id
stringlengths 11
11
| tags
stringlengths 10
777
| text
stringlengths 2
1.5k
| dataset_num
int64 1
3
| tokens
list | ner_tags
list |
|---|---|---|---|---|---|
NCT01908777
|
1:47:cancer
|
Subcutaneous panniculitis-like T-cell lymphoma
| 3
|
[
"Subcutaneous",
"panniculitis-like",
"T-cell",
"lymphoma"
] |
[
3,
3,
3,
3
] |
NCT03153319
|
1:27:treatment,
|
Immune suppression therapy less than 1 year prior to enrollment
| 3
|
[
"Immune",
"suppression",
"therapy",
"less",
"than",
"1",
"year",
"prior",
"to",
"enrollment"
] |
[
1,
1,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT01554371
|
59:69:allergy_name
|
Patients with known hypersensitivity to the components of study drug or its analogs
| 3
|
[
"Patients",
"with",
"known",
"hypersensitivity",
"to",
"the",
"components",
"of",
"study",
"drug",
"or",
"its",
"analogs"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
4,
4,
0,
0,
0
] |
NCT02925923
|
1:13:treatment
|
Voriconazole
| 3
|
[
"Voriconazole"
] |
[
1
] |
NCT02595372
|
75:89:allergy_name
|
Known hypersensitivity to any component of the formulation or substituted benzimidazoles
| 3
|
[
"Known",
"hypersensitivity",
"to",
"any",
"component",
"of",
"the",
"formulation",
"or",
"substituted",
"benzimidazoles"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4
] |
NCT01639508
|
,,52:77:treatment
|
Absolute neutrophil count (ANC) ≥ 1500/mm3 without colony stimulating factor support
| 3
|
[
"Absolute",
"neutrophil",
"count",
"(",
"ANC",
")",
"≥",
"1500/mm3",
"without",
"colony",
"stimulating",
"factor",
"support"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
0
] |
NCT01130077
|
43:49:chronic_disease,82:94:treatment,111:120:treatment
|
Newly diagnosed, non-brainstem high-grade glioma* Patients may not have received chemotherapy during or after radiation
| 3
|
[
"Newly",
"diagnosed",
",",
"non-brainstem",
"high-grade",
"glioma",
"*",
"Patients",
"may",
"not",
"have",
"received",
"chemotherapy",
"during",
"or",
"after",
"radiation"
] |
[
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
1
] |
NCT01841333
|
1:24:chronic_disease
|
Grade III/IV acute GVHD
| 3
|
[
"Grade",
"III/IV",
"acute",
"GVHD"
] |
[
2,
2,
2,
2
] |
NCT00739362
|
1:26:cancer,19:26:cancer,143:166:cancer
|
non-melanoma skin cancers or cancers that have clearly been cured or, in the opinion of the investigator, carry an excellent prognosis (e.g., Stage 1 cervical cancer)
| 3
|
[
"non-melanoma",
"skin",
"cancers",
"or",
"cancers",
"that",
"have",
"clearly",
"been",
"cured",
"or",
",",
"in",
"the",
"opinion",
"of",
"the",
"investigator",
",",
"carry",
"an",
"excellent",
"prognosis",
"(",
"e.g.",
",",
"Stage",
"1",
"cervical",
"cancer",
")"
] |
[
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
3,
3,
0
] |
NCT02139436
|
13:24:chronic_disease
|
significant arrhythmias
| 3
|
[
"significant",
"arrhythmias"
] |
[
0,
2
] |
NCT02746458
|
1:21:chronic_disease
|
Impaired circulation
| 3
|
[
"Impaired",
"circulation"
] |
[
2,
2
] |
NCT02181257
|
,41:51:treatment,75:103:treatment,133:141:treatment,149:159:treatment,,,283:307:chronic_disease
|
any patient who at least one year after transplant is treated with either lymphocyte depleting therapy or with an escalated dose of steroids (i.e., prednisone greater than 30 mg/day) for more than one month for an acute decline in lung function that is suspected to be secondary to acute cellular rejection
| 3
|
[
"any",
"patient",
"who",
"at",
"least",
"one",
"year",
"after",
"transplant",
"is",
"treated",
"with",
"either",
"lymphocyte",
"depleting",
"therapy",
"or",
"with",
"an",
"escalated",
"dose",
"of",
"steroids",
"(",
"i.e.",
",",
"prednisone",
"greater",
"than",
"30",
"mg/day",
")",
"for",
"more",
"than",
"one",
"month",
"for",
"an",
"acute",
"decline",
"in",
"lung",
"function",
"that",
"is",
"suspected",
"to",
"be",
"secondary",
"to",
"acute",
"cellular",
"rejection"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02928991
|
1:23:chronic_disease
|
Dyskeratosis Congenita
| 3
|
[
"Dyskeratosis",
"Congenita"
] |
[
2,
2
] |
NCT01690468
|
7:21:treatment
|
Prior TCN-PM therapy
| 3
|
[
"Prior",
"TCN-PM",
"therapy"
] |
[
0,
1,
1
] |
NCT01697371
|
1:11:cancer,
|
Metastases location within 2cm of GI tract
| 3
|
[
"Metastases",
"location",
"within",
"2cm",
"of",
"GI",
"tract"
] |
[
3,
0,
0,
0,
0,
0,
0
] |
NCT02579044
|
21:31:treatment
|
currently receiving lonafarnib under protocol 09-06-0298
| 3
|
[
"currently",
"receiving",
"lonafarnib",
"under",
"protocol",
"09-06-0298"
] |
[
0,
0,
1,
0,
0,
0
] |
NCT02480114
|
20:51:treatment
|
Planned primary or adjuvant chemoradiation therapy
| 3
|
[
"Planned",
"primary",
"or",
"adjuvant",
"chemoradiation",
"therapy"
] |
[
0,
0,
0,
1,
1,
1
] |
NCT01532687
|
,14:27:treatment,29:38:treatment,61:72:chronic_disease,,
|
Male partner sterilization (vasectomy with documentation of azoospermia) prior to the female subject's entry into the study, and this male is the sole partner for that subject
| 3
|
[
"Male",
"partner",
"sterilization",
"(",
"vasectomy",
"with",
"documentation",
"of",
"azoospermia",
")",
"prior",
"to",
"the",
"female",
"subject",
"'s",
"entry",
"into",
"the",
"study",
",",
"and",
"this",
"male",
"is",
"the",
"sole",
"partner",
"for",
"that",
"subject"
] |
[
0,
0,
1,
0,
1,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02505984
|
12:39:chronic_disease
|
At risk of postpartum depression (PPD)
| 3
|
[
"At",
"risk",
"of",
"postpartum",
"depression",
"(",
"PPD",
")"
] |
[
0,
0,
0,
2,
2,
2,
0,
0
] |
NCT01941316
|
23:38:chronic_disease,42:63:chronic_disease,,,,,122:135:chronic_disease,137:156:chronic_disease,176:199:chronic_disease,221:244:chronic_disease,246:265:chronic_disease,270:290:treatment,309:317:chronic_disease
|
Must not have had any unstable angina or myocardial infarction within 4 months prior to enrollment, NYHA Class III or IV heart failure, uncontrolled angina, history of severe coronary artery disease, severe uncontrolled ventricular arrhythmias, sick sinus syndrome, or electrocardiographic evidence of acute ischemia or Grade 3 conduction system abnormalities unless subject has a pacemaker
| 3
|
[
"Must",
"not",
"have",
"had",
"any",
"unstable",
"angina",
"or",
"myocardial",
"infarction",
"within",
"4",
"months",
"prior",
"to",
"enrollment",
",",
"NYHA",
"Class",
"III",
"or",
"IV",
"heart",
"failure",
",",
"uncontrolled",
"angina",
",",
"history",
"of",
"severe",
"coronary",
"artery",
"disease",
",",
"severe",
"uncontrolled",
"ventricular",
"arrhythmias",
",",
"sick",
"sinus",
"syndrome",
",",
"or",
"electrocardiographic",
"evidence",
"of",
"acute",
"ischemia",
"or",
"Grade",
"3",
"conduction",
"system",
"abnormalities",
"unless",
"subject",
"has",
"a",
"pacemaker"
] |
[
0,
0,
0,
0,
0,
2,
2,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
2,
2,
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
2,
2,
0,
2,
2,
2,
0,
0,
1,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01653093
|
1:44:chronic_disease
|
Acute or chronic severe renal insufficiency
| 3
|
[
"Acute",
"or",
"chronic",
"severe",
"renal",
"insufficiency"
] |
[
2,
2,
2,
2,
2,
2
] |
NCT03016351
|
1:21:chronic_disease
|
rheumatoid arthritis
| 3
|
[
"rheumatoid",
"arthritis"
] |
[
2,
2
] |
NCT01433965
|
,,30:45:treatment
|
Between 6 months to 8 months post transplant
| 3
|
[
"Between",
"6",
"months",
"to",
"8",
"months",
"post",
"transplant"
] |
[
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT03011567
|
1:34:chronic_disease
|
Preeclampsia with severe features
| 3
|
[
"Preeclampsia",
"with",
"severe",
"features"
] |
[
2,
2,
2,
2
] |
NCT02091141
|
4:22:treatment
|
No previous treatment with the specific assigned study drug or any other drug sharing the same target
| 3
|
[
"No",
"previous",
"treatment",
"with",
"the",
"specific",
"assigned",
"study",
"drug",
"or",
"any",
"other",
"drug",
"sharing",
"the",
"same",
"target"
] |
[
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02819440
|
12:24:chronic_disease
|
History of hearing loss
| 3
|
[
"History",
"of",
"hearing",
"loss"
] |
[
0,
0,
2,
2
] |
NCT02281409
|
16:43:treatment,
|
Any history of systemic anticancer therapy (standard or experimental) completed within 30 days prior to dosing
| 3
|
[
"Any",
"history",
"of",
"systemic",
"anticancer",
"therapy",
"(",
"standard",
"or",
"experimental",
")",
"completed",
"within",
"30",
"days",
"prior",
"to",
"dosing"
] |
[
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00919503
|
15:38:chronic_disease,,,,,,,
|
Patients with impaired renal function as evidenced by creatinine-clearance < 50% for age, weight, height or serum creatinine > 2 x upper normal limit or dialysis-dependent
| 3
|
[
"Patients",
"with",
"impaired",
"renal",
"function",
"as",
"evidenced",
"by",
"creatinine-clearance",
"<",
"50",
"%",
"for",
"age",
",",
"weight",
",",
"height",
"or",
"serum",
"creatinine",
">",
"2",
"x",
"upper",
"normal",
"limit",
"or",
"dialysis-dependent"
] |
[
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02481713
|
8:34:chronic_disease
|
severe auditory/visual impairment
| 3
|
[
"severe",
"auditory/visual",
"impairment"
] |
[
0,
2,
2
] |
NCT01976585
|
1:7:treatment,28:43:cancer,47:72:cancer,,,,135:161:cancer,166:183:cancer
|
Biopsy-confirmed low-grade B-cell lymphoma or cutaneous T cell lymphoma; specifically, follicular grade 1, 2, or 3A, marginal zone or small lymphocytic lymphoma, or mycosis fungoides of any initial stage
| 3
|
[
"Biopsy-confirmed",
"low-grade",
"B-cell",
"lymphoma",
"or",
"cutaneous",
"T",
"cell",
"lymphoma",
";",
"specifically",
",",
"follicular",
"grade",
"1",
",",
"2",
",",
"or",
"3A",
",",
"marginal",
"zone",
"or",
"small",
"lymphocytic",
"lymphoma",
",",
"or",
"mycosis",
"fungoides",
"of",
"any",
"initial",
"stage"
] |
[
1,
0,
3,
3,
0,
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
3,
0,
0,
3,
3,
0,
0,
0,
0
] |
NCT02309892
|
12:42:treatment,44:56:treatment,60:75:treatment
|
Concurrent chronic systemic immunotherapy, chemotherapy or hormone therapy
| 3
|
[
"Concurrent",
"chronic",
"systemic",
"immunotherapy",
",",
"chemotherapy",
"or",
"hormone",
"therapy"
] |
[
0,
1,
1,
1,
0,
1,
0,
1,
1
] |
NCT02418195
|
1:21:chronic_disease
|
Autoimmune hepatitis
| 3
|
[
"Autoimmune",
"hepatitis"
] |
[
2,
2
] |
NCT01869114
|
25:78:treatment,113:117:chronic_disease,133:150:treatment
|
Patients may have had a prior stem cell transplant (autologous or allogeneic), however they may not have active GvHD, nor be on any immunosuppression
| 3
|
[
"Patients",
"may",
"have",
"had",
"a",
"prior",
"stem",
"cell",
"transplant",
"(",
"autologous",
"or",
"allogeneic",
")",
",",
"however",
"they",
"may",
"not",
"have",
"active",
"GvHD",
",",
"nor",
"be",
"on",
"any",
"immunosuppression"
] |
[
0,
0,
0,
0,
0,
1,
1,
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
1
] |
NCT03006770
|
1:17:treatment,
|
minor amputation less than 2 weeks prior to screening
| 3
|
[
"minor",
"amputation",
"less",
"than",
"2",
"weeks",
"prior",
"to",
"screening"
] |
[
1,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02903446
|
14:28:chronic_disease
|
Uncontrolled hypothyroidism
| 3
|
[
"Uncontrolled",
"hypothyroidism"
] |
[
0,
2
] |
NCT00840047
|
80:98:chronic_disease
|
All participants under the care of St. Jude physicians with known or suspected neoplastic disease
| 3
|
[
"All",
"participants",
"under",
"the",
"care",
"of",
"St.",
"Jude",
"physicians",
"with",
"known",
"or",
"suspected",
"neoplastic",
"disease"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2
] |
NCT02564744
|
22:67:chronic_disease
|
Participants who are Hepatitis B surface antigen positive (HBsAg+) (must be PCR negative) who are taking antivirals, are allowed to enroll
| 3
|
[
"Participants",
"who",
"are",
"Hepatitis",
"B",
"surface",
"antigen",
"positive",
"(",
"HBsAg+",
")",
"(",
"must",
"be",
"PCR",
"negative",
")",
"who",
"are",
"taking",
"antivirals",
",",
"are",
"allowed",
"to",
"enroll"
] |
[
0,
0,
0,
2,
2,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03121352
|
28:59:treatment,
|
Patients who have received monoclonal anti-cancer antibody within 4 weeks of first dose of study drugs
| 3
|
[
"Patients",
"who",
"have",
"received",
"monoclonal",
"anti-cancer",
"antibody",
"within",
"4",
"weeks",
"of",
"first",
"dose",
"of",
"study",
"drugs"
] |
[
0,
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02249039
|
1:43:chronic_disease
|
Major Chromosomal anomaly (Trisomy 13, 18)
| 3
|
[
"Major",
"Chromosomal",
"anomaly",
"(",
"Trisomy",
"13",
",",
"18",
")"
] |
[
2,
2,
2,
2,
2,
2,
0,
0,
0
] |
NCT02512497
|
,113:123:treatment
|
Patients taking drugs leading to significant QT prolongation where the interaction is too great to proceed with romidepsin
| 3
|
[
"Patients",
"taking",
"drugs",
"leading",
"to",
"significant",
"QT",
"prolongation",
"where",
"the",
"interaction",
"is",
"too",
"great",
"to",
"proceed",
"with",
"romidepsin"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02479230
|
,,75:91:treatment
|
International normalized ratio (INR) < 1.5, except for subjects receiving warfarin therapy
| 3
|
[
"International",
"normalized",
"ratio",
"(",
"INR",
")",
"<",
"1.5",
",",
"except",
"for",
"subjects",
"receiving",
"warfarin",
"therapy"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02360579
|
25:31:chronic_disease,49:56:chronic_disease,,126:129:treatment,131:147:treatment,
|
At least one resectable lesion (or aggregate of lesions resected) of a minimum 1.5 cm in diameter post-resection to generate TIL; surgical removal with minimal morbidity (defined as any procedure for which expected hospitalization is ≤ 3 days)
| 3
|
[
"At",
"least",
"one",
"resectable",
"lesion",
"(",
"or",
"aggregate",
"of",
"lesions",
"resected",
")",
"of",
"a",
"minimum",
"1.5",
"cm",
"in",
"diameter",
"post-resection",
"to",
"generate",
"TIL",
";",
"surgical",
"removal",
"with",
"minimal",
"morbidity",
"(",
"defined",
"as",
"any",
"procedure",
"for",
"which",
"expected",
"hospitalization",
"is",
"≤",
"3",
"days",
")"
] |
[
0,
0,
0,
0,
2,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00881660
|
1:17:chronic_disease
|
Fetal aneuploidy, known structural genomic variants, other major fetal anomalies, or known syndromic mutation
| 3
|
[
"Fetal",
"aneuploidy",
",",
"known",
"structural",
"genomic",
"variants",
",",
"other",
"major",
"fetal",
"anomalies",
",",
"or",
"known",
"syndromic",
"mutation"
] |
[
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01624090
|
,,67:81:treatment,83:87:treatment,92:102:treatment
|
Cardiac Function: Left ventricular ejection fraction (EF) >40% by Echocardiogram, MUGA, or cardiac MR
| 3
|
[
"Cardiac",
"Function",
":",
"Left",
"ventricular",
"ejection",
"fraction",
"(",
"EF",
")",
">",
"40",
"%",
"by",
"Echocardiogram",
",",
"MUGA",
",",
"or",
"cardiac",
"MR"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
0,
1,
1
] |
NCT02538198
|
1:16:treatment
|
Bisphosphonates
| 3
|
[
"Bisphosphonates"
] |
[
1
] |
NCT02346201
|
5:50:chronic_disease,111:122:chronic_disease,,,163:188:chronic_disease,201:211:treatment,,,
|
Any cardiovascular or cerebrovascular abnormality deemed to be clinically significant by the study physician, tachycardia (heart rate > 100 beats per minute), or uncontrolled hypertension (defined as medication non-compliance or past 3 months with a diastolic reading > 105 mm Hg), at the time of screening
| 3
|
[
"Any",
"cardiovascular",
"or",
"cerebrovascular",
"abnormality",
"deemed",
"to",
"be",
"clinically",
"significant",
"by",
"the",
"study",
"physician",
",",
"tachycardia",
"(",
"heart",
"rate",
">",
"100",
"beats",
"per",
"minute",
")",
",",
"or",
"uncontrolled",
"hypertension",
"(",
"defined",
"as",
"medication",
"non-compliance",
"or",
"past",
"3",
"months",
"with",
"a",
"diastolic",
"reading",
">",
"105",
"mm",
"Hg",
")",
",",
"at",
"the",
"time",
"of",
"screening"
] |
[
0,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02371720
|
12:23:treatment,
|
Prescribed Hydroxyurea for at least the 6 months prior to study entry
| 3
|
[
"Prescribed",
"Hydroxyurea",
"for",
"at",
"least",
"the",
"6",
"months",
"prior",
"to",
"study",
"entry"
] |
[
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02835729
|
28:46:treatment,51:54:cancer,77:88:treatment,92:105:treatment
|
Patients who have received prior chemotherapy for AML with the exception of hydroxyurea or leukapheresis for leukocytosis
| 3
|
[
"Patients",
"who",
"have",
"received",
"prior",
"chemotherapy",
"for",
"AML",
"with",
"the",
"exception",
"of",
"hydroxyurea",
"or",
"leukapheresis",
"for",
"leukocytosis"
] |
[
0,
0,
0,
0,
1,
1,
0,
3,
0,
0,
0,
0,
1,
0,
1,
0,
0
] |
NCT02600897
|
6:17:chronic_disease,19:24:chronic_disease,29:45:chronic_disease
|
Poor hematologic, renal, or hepatic function
| 3
|
[
"Poor",
"hematologic",
",",
"renal",
",",
"or",
"hepatic",
"function"
] |
[
0,
2,
0,
2,
0,
0,
2,
2
] |
NCT01622868
|
,,42:53:treatment,,
|
Hemoglobin >= 8.0 g/dL (note: the use of transfusion or other intervention to achieve hemoglobin [Hgb] >= 8.0 g/dL is acceptable) (within 21 days prior to study entry)
| 3
|
[
"Hemoglobin",
">",
"=",
"8.0",
"g/dL",
"(",
"note",
":",
"the",
"use",
"of",
"transfusion",
"or",
"other",
"intervention",
"to",
"achieve",
"hemoglobin",
"[",
"Hgb",
"]",
">",
"=",
"8.0",
"g/dL",
"is",
"acceptable",
")",
"(",
"within",
"21",
"days",
"prior",
"to",
"study",
"entry",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02355002
|
41:50:treatment,58:71:chronic_disease,75:84:chronic_disease
|
Psychopathology not appropriate for the treatment (e.g., manic episode or psychosis)
| 3
|
[
"Psychopathology",
"not",
"appropriate",
"for",
"the",
"treatment",
"(",
"e.g.",
",",
"manic",
"episode",
"or",
"psychosis",
")"
] |
[
0,
0,
0,
0,
0,
1,
0,
0,
0,
2,
2,
0,
2,
0
] |
NCT02741180
|
15:31:chronic_disease
|
No history of heart arrhythmia
| 3
|
[
"No",
"history",
"of",
"heart",
"arrhythmia"
] |
[
0,
0,
0,
2,
2
] |
NCT01505062
|
22:59:allergy_name
|
Any known allergy to any component of the delivery vehicle
| 3
|
[
"Any",
"known",
"allergy",
"to",
"any",
"component",
"of",
"the",
"delivery",
"vehicle"
] |
[
0,
0,
0,
0,
4,
4,
4,
4,
4,
4
] |
NCT02048722
|
12:31:treatment,33:45:treatment,47:54:treatment,56:69:treatment,71:87:treatment,92:110:treatment,140:151:treatment
|
Concurrent anti-cancer therapy (chemotherapy, surgery, immunotherapy, biologic therapy, or tumor embolization) other than study treatment (regorafenib)
| 3
|
[
"Concurrent",
"anti-cancer",
"therapy",
"(",
"chemotherapy",
",",
"surgery",
",",
"immunotherapy",
",",
"biologic",
"therapy",
",",
"or",
"tumor",
"embolization",
")",
"other",
"than",
"study",
"treatment",
"(",
"regorafenib",
")"
] |
[
0,
1,
1,
0,
1,
0,
1,
0,
1,
0,
1,
1,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
1,
0
] |
NCT02587962
|
78:102:chronic_disease,104:116:chronic_disease,118:142:chronic_disease,144:162:chronic_disease,164:182:chronic_disease,186:207:chronic_disease,212:231:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, hypertension, unstable angina pectoris, cardiac arrhythmia, autoimmune disease or inflammatory diseases, or psychiatric illness/social situations that would limit compliance with study requirements
| 3
|
[
"Uncontrolled",
"intercurrent",
"illness",
"including",
",",
"but",
"not",
"limited",
"to",
",",
"symptomatic",
"congestive",
"heart",
"failure",
",",
"hypertension",
",",
"unstable",
"angina",
"pectoris",
",",
"cardiac",
"arrhythmia",
",",
"autoimmune",
"disease",
"or",
"inflammatory",
"diseases",
",",
"or",
"psychiatric",
"illness/social",
"situations",
"that",
"would",
"limit",
"compliance",
"with",
"study",
"requirements"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
0,
2,
0,
2,
2,
2,
0,
2,
2,
0,
2,
2,
0,
2,
2,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00715611
|
53:74:treatment
|
consideration should be given to drain the effusion prior to chemotherapy administration
| 3
|
[
"consideration",
"should",
"be",
"given",
"to",
"drain",
"the",
"effusion",
"prior",
"to",
"chemotherapy",
"administration"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
0
] |
NCT03007745
|
1:20:chronic_disease,29:35:chronic_disease,62:76:chronic_disease
|
central sleep apnea (50% of apneas on diagnostic testing are central apneas)
| 3
|
[
"central",
"sleep",
"apnea",
"(",
"50",
"%",
"of",
"apneas",
"on",
"diagnostic",
"testing",
"are",
"central",
"apneas",
")"
] |
[
2,
2,
2,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02796391
|
1:14:treatment
|
Phenobarbital
| 3
|
[
"Phenobarbital"
] |
[
1
] |
NCT02541903
|
44:72:chronic_disease
|
History or presence of clinically relevant cardiovascular abnormalities
| 3
|
[
"History",
"or",
"presence",
"of",
"clinically",
"relevant",
"cardiovascular",
"abnormalities"
] |
[
0,
0,
0,
0,
0,
0,
2,
2
] |
NCT02350764
|
19:33:cancer
|
All patients with adenocarcinoma histology must be tested for EGFR and ALK status
| 3
|
[
"All",
"patients",
"with",
"adenocarcinoma",
"histology",
"must",
"be",
"tested",
"for",
"EGFR",
"and",
"ALK",
"status"
] |
[
0,
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01754298
|
14:37:chronic_disease
|
Diagnosis of metabolic bone disorder
| 3
|
[
"Diagnosis",
"of",
"metabolic",
"bone",
"disorder"
] |
[
0,
0,
2,
2,
2
] |
NCT02354703
|
10:34:chronic_disease
|
Complete left bundle branch block
| 3
|
[
"Complete",
"left",
"bundle",
"branch",
"block"
] |
[
0,
2,
2,
2,
2
] |
NCT01920737
|
45:56:treatment
|
Active serious infections not controlled by antibiotics
| 3
|
[
"Active",
"serious",
"infections",
"not",
"controlled",
"by",
"antibiotics"
] |
[
0,
0,
0,
0,
0,
0,
1
] |
NCT02322203
|
21:47:treatment,78:85:treatment,87:95:treatment,100:122:treatment
|
Subjects taking any lipid modification therapy, including but not limited to statins, fibrates and bile acid sequestrants
| 3
|
[
"Subjects",
"taking",
"any",
"lipid",
"modification",
"therapy",
",",
"including",
"but",
"not",
"limited",
"to",
"statins",
",",
"fibrates",
"and",
"bile",
"acid",
"sequestrants"
] |
[
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1,
1,
1
] |
NCT02500602
|
17:41:treatment,30:41:treatment,,124:133:treatment
|
Subjects taking psychotropic medications will be required to be maintained on a stable dose for at least four weeks before treatment initiation. This is because initiation or change of medications during the course of the trial may interfere with interpretation of results
| 3
|
[
"Subjects",
"taking",
"psychotropic",
"medications",
"will",
"be",
"required",
"to",
"be",
"maintained",
"on",
"a",
"stable",
"dose",
"for",
"at",
"least",
"four",
"weeks",
"before",
"treatment",
"initiation",
".",
"This",
"is",
"because",
"initiation",
"or",
"change",
"of",
"medications",
"during",
"the",
"course",
"of",
"the",
"trial",
"may",
"interfere",
"with",
"interpretation",
"of",
"results"
] |
[
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01595529
|
67:97:treatment
|
Planned enrollment during this study coincides with enrollment in another therapeutic drug study
| 3
|
[
"Planned",
"enrollment",
"during",
"this",
"study",
"coincides",
"with",
"enrollment",
"in",
"another",
"therapeutic",
"drug",
"study"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
1
] |
NCT02566304
|
1:8:cancer,
|
Myeloma with < 5% plasma cells in the marrow
| 3
|
[
"Myeloma",
"with",
"<",
"5",
"%",
"plasma",
"cells",
"in",
"the",
"marrow"
] |
[
3,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02983240
|
1:14:chronic_disease
|
Fetal anomaly incompatible with life
| 3
|
[
"Fetal",
"anomaly",
"incompatible",
"with",
"life"
] |
[
2,
2,
0,
0,
0
] |
NCT00632853
|
54:72:treatment,89:100:treatment,127:138:treatment,142:151:treatment,156:165:treatment
|
Patients may have received one and only one cycle of chemotherapy prior to enrolling on CALGB 30610, which must have included carboplatin or cisplatin and etoposide
| 3
|
[
"Patients",
"may",
"have",
"received",
"one",
"and",
"only",
"one",
"cycle",
"of",
"chemotherapy",
"prior",
"to",
"enrolling",
"on",
"CALGB",
"30610",
",",
"which",
"must",
"have",
"included",
"carboplatin",
"or",
"cisplatin",
"and",
"etoposide"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1
] |
NCT03068130
|
107:125:treatment
|
Patients who have an ongoing SAE from a clinical study that is assessed by the investigator as related to bardoxolone methyl
| 3
|
[
"Patients",
"who",
"have",
"an",
"ongoing",
"SAE",
"from",
"a",
"clinical",
"study",
"that",
"is",
"assessed",
"by",
"the",
"investigator",
"as",
"related",
"to",
"bardoxolone",
"methyl"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02343042
|
33:58:treatment
|
Patients must not have received prior daratumumab therapy (Cohort 5.3 ONLY - dose expansion at RP2D)
| 3
|
[
"Patients",
"must",
"not",
"have",
"received",
"prior",
"daratumumab",
"therapy",
"(",
"Cohort",
"5.3",
"ONLY",
"-",
"dose",
"expansion",
"at",
"RP2D",
")"
] |
[
0,
0,
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01626079
|
47:69:allergy_name
|
Known hypersensitivity or contraindication to procedural medications which cannot be adequately managed medically
| 3
|
[
"Known",
"hypersensitivity",
"or",
"contraindication",
"to",
"procedural",
"medications",
"which",
"can",
"not",
"be",
"adequately",
"managed",
"medically"
] |
[
0,
0,
0,
0,
0,
4,
4,
0,
0,
0,
0,
0,
0,
0
] |
NCT02101034
|
74:96:treatment
|
Appropriate studies will be undertaken in patients receiving combination antiretroviral therapy when indicated
| 3
|
[
"Appropriate",
"studies",
"will",
"be",
"undertaken",
"in",
"patients",
"receiving",
"combination",
"antiretroviral",
"therapy",
"when",
"indicated"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0
] |
NCT02624258
|
,,69:79:treatment
|
A urine pregnancy test will be performed within 48 hours before the RNA CART19 infusion
| 3
|
[
"A",
"urine",
"pregnancy",
"test",
"will",
"be",
"performed",
"within",
"48",
"hours",
"before",
"the",
"RNA",
"CART19",
"infusion"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0
] |
NCT02656706
|
52:71:allergy_name
|
History of severe hypersensitivity reaction to any monoclonal antibody
| 3
|
[
"History",
"of",
"severe",
"hypersensitivity",
"reaction",
"to",
"any",
"monoclonal",
"antibody"
] |
[
0,
0,
0,
0,
0,
0,
0,
4,
4
] |
NCT02331095
|
1:13:treatment,
|
Thrombolysis within 6 weeks prior to enrollment
| 3
|
[
"Thrombolysis",
"within",
"6",
"weeks",
"prior",
"to",
"enrollment"
] |
[
1,
0,
0,
0,
0,
0,
0
] |
NCT02393794
|
34:50:cancer
|
Subjects with previously treated brain metastasis who are free of central nervous system (CNS) symptoms
| 3
|
[
"Subjects",
"with",
"previously",
"treated",
"brain",
"metastasis",
"who",
"are",
"free",
"of",
"central",
"nervous",
"system",
"(",
"CNS",
")",
"symptoms"
] |
[
0,
0,
0,
0,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02531880
|
86:94:chronic_disease,86:93:chronic_disease,,222:244:treatment,,
|
Drug resistant epilepsy participants will be defined as having clinically documented seizures with consistent EEG evidence as defined by the 1981 International Classification of Epileptic Seizures, refractory to standard anti-seizure treatment for at least one year prior to enrolling in this study and with an average of at least one seizure per month
| 3
|
[
"Drug",
"resistant",
"epilepsy",
"participants",
"will",
"be",
"defined",
"as",
"having",
"clinically",
"documented",
"seizures",
"with",
"consistent",
"EEG",
"evidence",
"as",
"defined",
"by",
"the",
"1981",
"International",
"Classification",
"of",
"Epileptic",
"Seizures",
",",
"refractory",
"to",
"standard",
"anti-seizure",
"treatment",
"for",
"at",
"least",
"one",
"year",
"prior",
"to",
"enrolling",
"in",
"this",
"study",
"and",
"with",
"an",
"average",
"of",
"at",
"least",
"one",
"seizure",
"per",
"month"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00969111
|
21:27:cancer,40:68:cancer,
|
Prior or concurrent cancer, other than non-melanomatous skin cancer, unless disease free for at least 5 years
| 3
|
[
"Prior",
"or",
"concurrent",
"cancer",
",",
"other",
"than",
"non-melanomatous",
"skin",
"cancer",
",",
"unless",
"disease",
"free",
"for",
"at",
"least",
"5",
"years"
] |
[
0,
0,
0,
3,
0,
0,
0,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02710240
|
28:34:allergy_name
|
Subjects with a history of iodide allergies
| 3
|
[
"Subjects",
"with",
"a",
"history",
"of",
"iodide",
"allergies"
] |
[
0,
0,
0,
0,
0,
4,
0
] |
NCT03170453
|
10:57:chronic_disease
|
Comorbid attention deficit hyperactivity disorder (ADHD) that is untreated
| 3
|
[
"Comorbid",
"attention",
"deficit",
"hyperactivity",
"disorder",
"(",
"ADHD",
")",
"that",
"is",
"untreated"
] |
[
0,
2,
2,
2,
2,
2,
0,
0,
0,
0,
0
] |
NCT01581580
|
8:21:chronic_disease
|
active heart disease needing immediate intervention
| 3
|
[
"active",
"heart",
"disease",
"needing",
"immediate",
"intervention"
] |
[
0,
2,
2,
0,
0,
0
] |
NCT01989585
|
47:63:chronic_disease,79:102:treatment,126:136:treatment,153:164:treatment,166:175:treatment,177:186:treatment,188:196:treatment,208:222:treatment,224:229:treatment,234:252:treatment,328:355:treatment,365:372:treatment,417:445:treatment,447:454:treatment,,611:626:treatment,631:641:chronic_disease,,,,,829:859:treatment
|
Due to the expected dose-limiting toxicity of thrombocytopenia, the following concomitant medications are not allowed during navitoclax administration: clopidogrel, ibuprofen, tirofiban, warfarin, and other anticoagulants, drugs, or herbal supplements that affect platelet function are excluded, with the exception of low-dose anticoagulation medications (such as heparin) that are used to maintain the patency of a central intravenous catheter; aspirin will not be allowed within 7 days prior to the first dose of navitoclax or during navitoclax administration; however, subjects who have previously received aspirin therapy for thrombosis prevention may resume a low dose (i.e., maximum 100 mg QD) of aspirin if platelet counts are stable (>= 50,000/mm^3) through 6 weeks of navitoclax administration; all decisions regarding treatment with aspirin therapy will be determined by the investigator in conjunction with the medical monitor
| 3
|
[
"Due",
"to",
"the",
"expected",
"dose-limiting",
"toxicity",
"of",
"thrombocytopenia",
",",
"the",
"following",
"concomitant",
"medications",
"are",
"not",
"allowed",
"during",
"navitoclax",
"administration",
":",
"clopidogrel",
",",
"ibuprofen",
",",
"tirofiban",
",",
"warfarin",
",",
"and",
"other",
"anticoagulants",
",",
"drugs",
",",
"or",
"herbal",
"supplements",
"that",
"affect",
"platelet",
"function",
"are",
"excluded",
",",
"with",
"the",
"exception",
"of",
"low-dose",
"anticoagulation",
"medications",
"(",
"such",
"as",
"heparin",
")",
"that",
"are",
"used",
"to",
"maintain",
"the",
"patency",
"of",
"a",
"central",
"intravenous",
"catheter",
";",
"aspirin",
"will",
"not",
"be",
"allowed",
"within",
"7",
"days",
"prior",
"to",
"the",
"first",
"dose",
"of",
"navitoclax",
"or",
"during",
"navitoclax",
"administration",
";",
"however",
",",
"subjects",
"who",
"have",
"previously",
"received",
"aspirin",
"therapy",
"for",
"thrombosis",
"prevention",
"may",
"resume",
"a",
"low",
"dose",
"(",
"i.e.",
",",
"maximum",
"100",
"mg",
"QD",
")",
"of",
"aspirin",
"if",
"platelet",
"counts",
"are",
"stable",
"(",
">",
"=",
"50,000/mm^3",
")",
"through",
"6",
"weeks",
"of",
"navitoclax",
"administration",
";",
"all",
"decisions",
"regarding",
"treatment",
"with",
"aspirin",
"therapy",
"will",
"be",
"determined",
"by",
"the",
"investigator",
"in",
"conjunction",
"with",
"the",
"medical",
"monitor"
] |
[
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
1,
1,
0,
0,
0,
0,
1,
0,
0,
1,
0,
1,
0,
1,
0,
1,
0,
0,
0,
1,
0,
1,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01970176
|
22:35:chronic_disease,,,,,
|
Patients with severe liver disease (AST > 3x normal, alkaline phosphatase or bilirubin > 2x normal)
| 3
|
[
"Patients",
"with",
"severe",
"liver",
"disease",
"(",
"AST",
">",
"3x",
"normal",
",",
"alkaline",
"phosphatase",
"or",
"bilirubin",
">",
"2x",
"normal",
")"
] |
[
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02521103
|
79:101:treatment
|
Patient is a candidate for revision of all femoral and tibial components of a total knee replacement
| 3
|
[
"Patient",
"is",
"a",
"candidate",
"for",
"revision",
"of",
"all",
"femoral",
"and",
"tibial",
"components",
"of",
"a",
"total",
"knee",
"replacement"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02353728
|
1:29:chronic_disease
|
Cytogenetic clonal evolution
| 3
|
[
"Cytogenetic",
"clonal",
"evolution"
] |
[
2,
2,
2
] |
NCT02140554
|
13:16:chronic_disease
|
Have severe SCD
| 3
|
[
"Have",
"severe",
"SCD"
] |
[
0,
0,
2
] |
NCT01990209
|
11:31:treatment,,,107:116:treatment,132:141:treatment
|
Use of an investigational drug ≤21 days or 5 half-lives (whichever is shorter) prior to the first dose of orteronel, or concurrent treatment
| 3
|
[
"Use",
"of",
"an",
"investigational",
"drug",
"≤21",
"days",
"or",
"5",
"half-lives",
"(",
"whichever",
"is",
"shorter",
")",
"prior",
"to",
"the",
"first",
"dose",
"of",
"orteronel",
",",
"or",
"concurrent",
"treatment"
] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
1
] |
NCT01461837
|
1:4:chronic_disease
|
SCD patients who have an unaffected HLA matched family donor willing to proceed to donation
| 3
|
[
"SCD",
"patients",
"who",
"have",
"an",
"unaffected",
"HLA",
"matched",
"family",
"donor",
"willing",
"to",
"proceed",
"to",
"donation"
] |
[
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02304458
|
54:71:chronic_disease
|
Parts A & C: patients must have either measurable or evaluable disease
| 3
|
[
"Parts",
"A",
"&",
"C",
":",
"patients",
"must",
"have",
"either",
"measurable",
"or",
"evaluable",
"disease"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2
] |
NCT03018704
|
1:23:treatment
|
bilateral oophorectomy
| 3
|
[
"bilateral",
"oophorectomy"
] |
[
1,
1
] |
NCT00977977
|
28:39:chronic_disease,114:123:treatment,186:206:chronic_disease
|
Patients with a history of arrhythmias will be evaluated by a cardiology consultant regarding recommendations as Rituximab has been reported to exacerbate arrhythmias (in patients with rheumatoid arthritis)
| 3
|
[
"Patients",
"with",
"a",
"history",
"of",
"arrhythmias",
"will",
"be",
"evaluated",
"by",
"a",
"cardiology",
"consultant",
"regarding",
"recommendations",
"as",
"Rituximab",
"has",
"been",
"reported",
"to",
"exacerbate",
"arrhythmias",
"(",
"in",
"patients",
"with",
"rheumatoid",
"arthritis",
")"
] |
[
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0
] |
NCT02566304
|
1:7:chronic_disease,9:18:cancer,23:30:cancer,,137:144:treatment,149:163:treatment,167:186:treatment,209:218:treatment
|
RAEB-1, RCMD+/-RS, or MDS NOS with stable disease for 6 months (as documented by serial bone marrow examinations) in the absence of any therapy but growth factors or transfusion support. Patients who require treatment to control their disease must show chemo-responsiveness
| 3
|
[
"RAEB-1",
",",
"RCMD+/-RS",
",",
"or",
"MDS",
"NOS",
"with",
"stable",
"disease",
"for",
"6",
"months",
"(",
"as",
"documented",
"by",
"serial",
"bone",
"marrow",
"examinations",
")",
"in",
"the",
"absence",
"of",
"any",
"therapy",
"but",
"growth",
"factors",
"or",
"transfusion",
"support",
".",
"Patients",
"who",
"require",
"treatment",
"to",
"control",
"their",
"disease",
"must",
"show",
"chemo-responsiveness"
] |
[
2,
0,
3,
0,
0,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
1,
0,
1,
1,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT01096368
|
64:87:cancer,111:130:cancer,134:165:cancer
|
Patients must be newly diagnosed with histologically confirmed intracranial ependymoma; patients with classic ependymoma (WHO II) or anaplastic ependymoma (WHO III) are eligible, as are various subtypes described as clear cell, papillary, cellular or a combination of the above
| 3
|
[
"Patients",
"must",
"be",
"newly",
"diagnosed",
"with",
"histologically",
"confirmed",
"intracranial",
"ependymoma",
";",
"patients",
"with",
"classic",
"ependymoma",
"(",
"WHO",
"II",
")",
"or",
"anaplastic",
"ependymoma",
"(",
"WHO",
"III",
")",
"are",
"eligible",
",",
"as",
"are",
"various",
"subtypes",
"described",
"as",
"clear",
"cell",
",",
"papillary",
",",
"cellular",
"or",
"a",
"combination",
"of",
"the",
"above"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03070535
|
1:26:chronic_disease
|
Mild cognitive impairment with no functional deficits is ok
| 3
|
[
"Mild",
"cognitive",
"impairment",
"with",
"no",
"functional",
"deficits",
"is",
"ok"
] |
[
2,
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT01896999
|
,48:58:treatment,,,
|
continuing for 5 months after the last dose of study drug (for female patients) and for 7 months after the last dose of study drug (for male patients who are sexually active with WOCBP)
| 3
|
[
"continuing",
"for",
"5",
"months",
"after",
"the",
"last",
"dose",
"of",
"study",
"drug",
"(",
"for",
"female",
"patients",
")",
"and",
"for",
"7",
"months",
"after",
"the",
"last",
"dose",
"of",
"study",
"drug",
"(",
"for",
"male",
"patients",
"who",
"are",
"sexually",
"active",
"with",
"WOCBP",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02379520
|
30:46:treatment
|
patient is unable to receive standard therapy
| 3
|
[
"patient",
"is",
"unable",
"to",
"receive",
"standard",
"therapy"
] |
[
0,
0,
0,
0,
0,
1,
1
] |
NCT02497300
|
1:22:chronic_disease,
|
myocardial infarction within the past 6 months
| 3
|
[
"myocardial",
"infarction",
"within",
"the",
"past",
"6",
"months"
] |
[
2,
2,
0,
0,
0,
0,
0
] |
NCT03018704
|
34:37:allergy_name
|
a history of hypersensitivity to TOP
| 3
|
[
"a",
"history",
"of",
"hypersensitivity",
"to",
"TOP"
] |
[
0,
0,
0,
0,
0,
4
] |
NCT02890979
|
34:52:chronic_disease
|
Subjects with known or suspected esophageal varices
| 3
|
[
"Subjects",
"with",
"known",
"or",
"suspected",
"esophageal",
"varices"
] |
[
0,
0,
0,
0,
0,
2,
2
] |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.