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list | ner_tags
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|---|---|---|---|---|---|
NCT02236013
|
1:21:treatment,,
|
Preemptive treatment with retinoic acid prior to exclusion of APL ≤ 7 days
| 3
|
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NCT02349958
|
9:19:cancer,50:63:chronic_disease,58:63:cancer,
|
Uterine malignancy of the corpus, or cervix with primary tumor Stage IIIA or greater, or recurrent tumor confined to the abdomen
| 3
|
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NCT03028012
|
1:27:chronic_disease
|
Pre-existing renal disease
| 3
|
[
"Pre-existing",
"renal",
"disease"
] |
[
2,
2,
2
] |
NCT02497690
|
8:24:chronic_disease
|
severe motor impairment
| 3
|
[
"severe",
"motor",
"impairment"
] |
[
0,
2,
2
] |
NCT02514070
|
12:27:cancer
|
History of prostate Cancer
| 3
|
[
"History",
"of",
"prostate",
"Cancer"
] |
[
0,
0,
3,
3
] |
NCT02932280
|
,,24:35:treatment,
|
Hemoglobin < 8.0 g/dL (transfusion permitted at least 7 days prior to baseline)
| 3
|
[
"Hemoglobin",
"<",
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"transfusion",
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NCT01799135
|
37:78:treatment
|
Adequate renal function to tolerate intravenous gadolinium contrast injection
| 3
|
[
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"renal",
"function",
"to",
"tolerate",
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"gadolinium",
"contrast",
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0,
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0,
0,
1,
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1,
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NCT01312857
|
37:62:cancer,63:86:cancer,132:152:chronic_disease
|
History of histologically confirmed colorectal adenocarcinoma metastatic to the liver with no clinical or radiographic evidence of extrahepatic disease
| 3
|
[
"History",
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"colorectal",
"adenocarcinoma",
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"to",
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"liver",
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NCT02374918
|
35:39:chronic_disease
|
The occurrence of a concussion or mTBI must be documented by a medical report or other professional witness documentation
| 3
|
[
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"a",
"concussion",
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NCT02464878
|
1:15:chronic_disease,
|
AAT deficiency (defined as < 1.0ng/mg AAT)
| 3
|
[
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0,
0,
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0,
0,
0,
0
] |
NCT02697201
|
1:10:chronic_disease
|
Sedentary
| 3
|
[
"Sedentary"
] |
[
2
] |
NCT02754752
|
1:36:cancer
|
Metastatic breast cancer (stage IV)
| 3
|
[
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"breast",
"cancer",
"(",
"stage",
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")"
] |
[
3,
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NCT02950337
|
22:61:chronic_disease
|
Patients with severe obstructive or restrictive lung disease
| 3
|
[
"Patients",
"with",
"severe",
"obstructive",
"or",
"restrictive",
"lung",
"disease"
] |
[
0,
0,
0,
2,
2,
2,
2,
2
] |
NCT03093272
|
1:16:cancer
|
Prostate cancer progression on or since last treatment as documented by PSA rise or bone progression according to PCWG2 or soft tissue radiographic progression according to RECIST criteria Version 1.1
| 3
|
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NCT02033616
|
28:44:cancer,73:98:treatment,136:147:treatment,151:161:treatment,238:247:treatment
|
Patients with one or a few brain metastases that have been treated with stereotactic radiotherapy consisting of a single dose, such as Gamma Knife or Cyberknife, are allowed to be included in the study, but need wait one week after such treatment
| 3
|
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NCT02628535
|
18:44:chronic_disease,18:29:chronic_disease,72:115:chronic_disease,120:131:chronic_disease
|
Known history of hepatitis B or C infection or known positive test for hepatitis B surface antigen or core antigen, or hepatitis C polymerase chain reaction (PCR)
| 3
|
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NCT02520427
|
12:31:chronic_disease,37:43:chronic_disease,47:72:chronic_disease,,95:104:chronic_disease,115:138:treatment,
|
History of arterial thrombosis (eg, stroke or transient ischemic attack) in the past 3 months Infection requiring intravenous antibiotics within 1 week of study enrollment (day 1)
| 3
|
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"History",
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"thrombosis",
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NCT02367196
|
24:36:cancer
|
relapsed or refractory solid tumors
| 3
|
[
"relapsed",
"or",
"refractory",
"solid",
"tumors"
] |
[
0,
0,
0,
3,
3
] |
NCT02901041
|
1:17:chronic_disease
|
Bipolar disorder
| 3
|
[
"Bipolar",
"disorder"
] |
[
2,
2
] |
NCT02101736
|
1:25:chronic_disease
|
unstable angina pectoris
| 3
|
[
"unstable",
"angina",
"pectoris"
] |
[
2,
2,
2
] |
NCT02388685
|
27:41:chronic_disease
|
heel cord contracture and foot deformity
| 3
|
[
"heel",
"cord",
"contracture",
"and",
"foot",
"deformity"
] |
[
0,
0,
0,
0,
2,
2
] |
NCT02875301
|
1:3:chronic_disease
|
MS
| 3
|
[
"MS"
] |
[
2
] |
NCT02311621
|
23:54:treatment
|
Must not be receiving external beam radiation therapy at the time of study enrollment
| 3
|
[
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"external",
"beam",
"radiation",
"therapy",
"at",
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NCT02235857
|
1:32:treatment,47:65:chronic_disease,82:94:chronic_disease
|
Pediatric post renal transplant patients with nephrotic syndrome associated with primary FSGS
| 3
|
[
"Pediatric",
"post",
"renal",
"transplant",
"patients",
"with",
"nephrotic",
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NCT02350764
|
6:22:cancer
|
Have residual disease following surgical resection that is measurable by RECIST v1.1
| 3
|
[
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"surgical",
"resection",
"that",
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NCT02964741
|
1:18:treatment
|
Prior use of tDCS
| 3
|
[
"Prior",
"use",
"of",
"tDCS"
] |
[
1,
1,
1,
1
] |
NCT01734512
|
23:32:treatment,34:46:treatment,54:66:treatment
|
Patients may have had treatment (chemotherapy and/or radiotherapy) for any number of relapses prior to this recurrence
| 3
|
[
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NCT02081404
|
1:21:chronic_disease
|
Peptic ulcer disease
| 3
|
[
"Peptic",
"ulcer",
"disease"
] |
[
2,
2,
2
] |
NCT02353728
|
12:28:chronic_disease
|
Congenital long QT syndrome or a known family history of long QT syndrome
| 3
|
[
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"long",
"QT",
"syndrome",
"or",
"a",
"known",
"family",
"history",
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[
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NCT02315612
|
43:55:chronic_disease
|
A subject will not be excluded because of pancytopenia related to disease
| 3
|
[
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"be",
"excluded",
"because",
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NCT03032328
|
32:41:chronic_disease,43:53:chronic_disease,58:78:chronic_disease,119:144:chronic_disease
|
Patients will be excluded if a metabolic, mechanical, or mucosal inflammatory cause has been defined to explain their gastrointestinal symptoms
| 3
|
[
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NCT02393157
|
7:47:chronic_disease
|
Known congenital or acquired immune deficiency
| 3
|
[
"Known",
"congenital",
"or",
"acquired",
"immune",
"deficiency"
] |
[
0,
2,
2,
2,
2,
2
] |
NCT02503722
|
1:26:chronic_disease
|
Uncontrolled hypertension
| 3
|
[
"Uncontrolled",
"hypertension"
] |
[
2,
2
] |
NCT02445339
|
1:19:chronic_disease,,
|
Acute liver injury (liver aminotransferase concentrations >5 times the upper limit of normal)
| 3
|
[
"Acute",
"liver",
"injury",
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"liver",
"aminotransferase",
"concentrations",
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"the",
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NCT01624090
|
15:34:cancer
|
Patients with cerebral metastases
| 3
|
[
"Patients",
"with",
"cerebral",
"metastases"
] |
[
0,
0,
3,
3
] |
NCT02382419
|
11:31:treatment,
|
Use of an investigational drug in the 3 months prior to screening and must agree to not participate in any drug or device study while enrolled in this study
| 3
|
[
"Use",
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"drug",
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NCT02251431
|
8:23:treatment
|
Use of DDP4 inhibitors
| 3
|
[
"Use",
"of",
"DDP4",
"inhibitors"
] |
[
0,
0,
1,
1
] |
NCT03108950
|
1:25:chronic_disease
|
Severe pulmonary disease
| 3
|
[
"Severe",
"pulmonary",
"disease"
] |
[
2,
2,
2
] |
NCT02278250
|
,,,,137:147:treatment
|
Men with pregnant or lactating partners or partners who plan to become pregnant during the study or within 6 months of the last dose of study drug
| 3
|
[
"Men",
"with",
"pregnant",
"or",
"lactating",
"partners",
"or",
"partners",
"who",
"plan",
"to",
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"pregnant",
"during",
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NCT01823198
|
1:26:cancer
|
Myelodysplastic syndromes with intermediat
| 3
|
[
"Myelodysplastic",
"syndromes",
"with",
"intermediat"
] |
[
3,
3,
0,
0
] |
NCT02512926
|
,55:80:treatment
|
At least 14 days must have elapsed since last dose of pegfilgrastim (Neulasta®)
| 3
|
[
"At",
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"days",
"must",
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0,
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NCT02267863
|
5:28:treatment,,,71:90:treatment,112:121:treatment
|
Off previous cancer therapy for at least 14 days, or 5 half-lives for noncytotoxic agents prior to first study treatment administration
| 3
|
[
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NCT02593123
|
45:71:cancer
|
Any of the following high risk or recurrent hematological malignancies
| 3
|
[
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"or",
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NCT02985554
|
23:35:treatment,39:51:treatment,96:107:treatment
|
Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events (AEs) due to agents administered more than 4 weeks earlier
| 3
|
[
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"due",
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"administered",
"more",
"than",
"4",
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"earlier"
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NCT02709980
|
1:12:chronic_disease
|
Sleep apnea
| 3
|
[
"Sleep",
"apnea"
] |
[
2,
2
] |
NCT02554253
|
21:44:treatment
|
schedule to undergo complex cardiac surgery
| 3
|
[
"schedule",
"to",
"undergo",
"complex",
"cardiac",
"surgery"
] |
[
0,
0,
0,
1,
1,
1
] |
NCT01505569
|
1:34:cancer,,
|
Primary Malignant Brain Neoplasms <18 years of age - at diagnosis and/or relapse
| 3
|
[
"Primary",
"Malignant",
"Brain",
"Neoplasms",
"<",
"18",
"years",
"of",
"age",
"-",
"at",
"diagnosis",
"and/or",
"relapse"
] |
[
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02778867
|
17:35:chronic_disease
|
Have concurrent H pylori gastritis
| 3
|
[
"Have",
"concurrent",
"H",
"pylori",
"gastritis"
] |
[
0,
0,
2,
2,
2
] |
NCT02366871
|
13:19:treatment
|
Concomitant NSAIDS
| 3
|
[
"Concomitant",
"NSAIDS"
] |
[
0,
1
] |
NCT02468453
|
17:22:treatment,23:31:treatment,32:46:treatment,67:115:treatment,,155:164:treatment
|
Having received Botox/collagen/fat injections or other methods of augmentation with injected or implanted material in the treated area within 9 months of treatment or during the study (if face is treated)
| 3
|
[
"Having",
"received",
"Botox/collagen/fat",
"injections",
"or",
"other",
"methods",
"of",
"augmentation",
"with",
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"implanted",
"material",
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NCT01389024
|
9:34:treatment
|
Chronic blood transfusion therapy, ongoing or planned
| 3
|
[
"Chronic",
"blood",
"transfusion",
"therapy",
",",
"ongoing",
"or",
"planned"
] |
[
0,
1,
1,
1,
0,
0,
0,
0
] |
NCT02833207
|
,31:51:treatment
|
Regularly (≥5 days/week) take acetylsalicylic acid
| 3
|
[
"Regularly",
"(",
"≥5",
"days/week",
")",
"take",
"acetylsalicylic",
"acid"
] |
[
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT03158974
|
182:204:treatment
|
Are willing and able to participate as an outpatient, making regularly scheduled visits to the study center during the treatment and to comply with all study requirements including concomitant medication and other treatment restrictions
| 3
|
[
"Are",
"willing",
"and",
"able",
"to",
"participate",
"as",
"an",
"outpatient",
",",
"making",
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"scheduled",
"visits",
"to",
"the",
"study",
"center",
"during",
"the",
"treatment",
"and",
"to",
"comply",
"with",
"all",
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"requirements",
"including",
"concomitant",
"medication",
"and",
"other",
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] |
NCT02706353
|
26:48:cancer
|
Patients with history of hematologic malignancy
| 3
|
[
"Patients",
"with",
"history",
"of",
"hematologic",
"malignancy"
] |
[
0,
0,
0,
0,
3,
3
] |
NCT02675114
|
8:28:chronic_disease,
|
Severe aortic regurgitation (>3+)
| 3
|
[
"Severe",
"aortic",
"regurgitation",
"(",
">",
"3+",
")"
] |
[
0,
2,
2,
0,
0,
0,
0
] |
NCT03159702
|
,,,264:292:treatment,
|
Females of child bearing potential should agree to practice 2 effective methods of contraception, at the same time, from the time of signing the informed consent form through 90 days after the last dose of study drug and must also adhere to the guidelines of any treatment-specific pregnancy prevention program, if applicable, or agree to practice true abstinence when this is in line with the preferred and usual lifestyle of the subject
| 3
|
[
"Females",
"of",
"child",
"bearing",
"potential",
"should",
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"to",
"practice",
"2",
"effective",
"methods",
"of",
"contraception",
",",
"at",
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"same",
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",",
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NCT03053453
|
1:26:chronic_disease
|
Ligamentous Insufficiency
| 3
|
[
"Ligamentous",
"Insufficiency"
] |
[
2,
2
] |
NCT02323191
|
86:126:cancer,128:142:cancer,144:158:cancer,160:174:cancer,179:198:cancer
|
Participants must have histologically confirmed diagnosis of locally advanced and/or metastatic triple negative breast cancer, ovarian cancer, bladder cancer, gastric cancer, or soft tissue sarcoma
| 3
|
[
"Participants",
"must",
"have",
"histologically",
"confirmed",
"diagnosis",
"of",
"locally",
"advanced",
"and/or",
"metastatic",
"triple",
"negative",
"breast",
"cancer",
",",
"ovarian",
"cancer",
",",
"bladder",
"cancer",
",",
"gastric",
"cancer",
",",
"or",
"soft",
"tissue",
"sarcoma"
] |
[
0,
0,
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3,
3,
0,
3,
3,
0,
3,
3,
0,
0,
3,
3,
3
] |
NCT02188745
|
18:23:cancer,69:75:treatment,,,151:162:treatment,166:181:treatment,208:212:treatment
|
Freshly acquired tumor specimens: As part of a clinically indicated biopsy procedure, an additional 1-3 cores or tissue fragments will be obtained by core needle or surgical biopsy for research purposes and FFPE
| 3
|
[
"Freshly",
"acquired",
"tumor",
"specimens",
":",
"As",
"part",
"of",
"a",
"clinically",
"indicated",
"biopsy",
"procedure",
",",
"an",
"additional",
"1-3",
"cores",
"or",
"tissue",
"fragments",
"will",
"be",
"obtained",
"by",
"core",
"needle",
"or",
"surgical",
"biopsy",
"for",
"research",
"purposes",
"and",
"FFPE"
] |
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1,
0,
1,
1,
0,
0,
0,
0,
1
] |
NCT01951885
|
1:17:cancer
|
Multiple myeloma
| 3
|
[
"Multiple",
"myeloma"
] |
[
3,
3
] |
NCT02317991
|
37:49:chronic_disease,51:62:chronic_disease,83:88:chronic_disease,105:115:chronic_disease,117:133:chronic_disease,135:152:chronic_disease,154:168:chronic_disease,170:193:chronic_disease,195:213:chronic_disease,217:229:chronic_disease
|
Evidence or history of uncontrolled hypertension, proteinuria, non-healing wound, ulcer, bone fracture, hemoptysis, valvular disease, abdominal fistula, GI perforation, intra-abdominal abscess, bleeding diathesis or coagulopathy
| 3
|
[
"Evidence",
"or",
"history",
"of",
"uncontrolled",
"hypertension",
",",
"proteinuria",
",",
"non-healing",
"wound",
",",
"ulcer",
",",
"bone",
"fracture",
",",
"hemoptysis",
",",
"valvular",
"disease",
",",
"abdominal",
"fistula",
",",
"GI",
"perforation",
",",
"intra-abdominal",
"abscess",
",",
"bleeding",
"diathesis",
"or",
"coagulopathy"
] |
[
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2,
0,
2,
2,
0,
2,
2,
0,
2,
2,
0,
2,
2,
0,
2
] |
NCT02557321
|
,,190:195:treatment
|
At least 1 Injectable Lesion (i.e., cutaneous, subcutaneous, soft tissue, superficial nodal or palpable nodal lesion with longest diameter at least 5 mm that is suitable for injection with PV-10)
| 3
|
[
"At",
"least",
"1",
"Injectable",
"Lesion",
"(",
"i.e.",
",",
"cutaneous",
",",
"subcutaneous",
",",
"soft",
"tissue",
",",
"superficial",
"nodal",
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"palpable",
"nodal",
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"with",
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"diameter",
"at",
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"5",
"mm",
"that",
"is",
"suitable",
"for",
"injection",
"with",
"PV-10",
")"
] |
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0,
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0,
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0,
0,
0,
1,
0
] |
NCT01967823
|
,,52:62:treatment
|
ANC greater than 1000/mm(3) without the support of filgrastim
| 3
|
[
"ANC",
"greater",
"than",
"1000/mm",
"(",
"3",
")",
"without",
"the",
"support",
"of",
"filgrastim"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT03111121
|
41:51:allergy_name
|
Patients with contraindications towards sugammadex
| 3
|
[
"Patients",
"with",
"contraindications",
"towards",
"sugammadex"
] |
[
0,
0,
0,
0,
4
] |
NCT02210078
|
34:44:chronic_disease
|
Patients with other uncontrolled infections
| 3
|
[
"Patients",
"with",
"other",
"uncontrolled",
"infections"
] |
[
0,
0,
0,
0,
2
] |
NCT02502799
|
14:18:chronic_disease
|
Diagnosis of ADHD
| 3
|
[
"Diagnosis",
"of",
"ADHD"
] |
[
0,
0,
2
] |
NCT02122185
|
27:55:treatment
|
subjects who will undergo intraperitoneal chemotherapy
| 3
|
[
"subjects",
"who",
"will",
"undergo",
"intraperitoneal",
"chemotherapy"
] |
[
0,
0,
0,
0,
1,
1
] |
NCT03035890
|
1:17:chronic_disease
|
hepatitis B or C
| 3
|
[
"hepatitis",
"B",
"or",
"C"
] |
[
2,
2,
2,
2
] |
NCT02442297
|
53:75:treatment,
|
Subjects should have been off other investigational antineoplastic therapy for two weeks prior to entry in this study
| 3
|
[
"Subjects",
"should",
"have",
"been",
"off",
"other",
"investigational",
"antineoplastic",
"therapy",
"for",
"two",
"weeks",
"prior",
"to",
"entry",
"in",
"this",
"study"
] |
[
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02763228
|
1:23:cancer
|
Stage IV breast cancer
| 3
|
[
"Stage",
"IV",
"breast",
"cancer"
] |
[
3,
3,
3,
3
] |
NCT02058095
|
15:35:chronic_disease,59:87:chronic_disease,113:124:chronic_disease,140:158:chronic_disease
|
Patients with retinitis pigmentosa, previous diagnosis of nonischemic optic neuropathy, untreated proliferative retinopathy or unexplained visual disturbance
| 3
|
[
"Patients",
"with",
"retinitis",
"pigmentosa",
",",
"previous",
"diagnosis",
"of",
"nonischemic",
"optic",
"neuropathy",
",",
"untreated",
"proliferative",
"retinopathy",
"or",
"unexplained",
"visual",
"disturbance"
] |
[
0,
0,
2,
2,
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
2,
0,
0,
2,
2
] |
NCT02514083
|
1:23:chronic_disease,57:82:chronic_disease,87:148:chronic_disease,150:188:chronic_disease,193:230:chronic_disease
|
Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel or ulcerative colitis, symptomatic inflammatory bowel disease, or partial or complete bowel obstruction
| 3
|
[
"Malabsorption",
"syndrome",
",",
"disease",
"significantly",
"affecting",
"gastrointestinal",
"function",
",",
"or",
"resection",
"of",
"the",
"stomach",
"or",
"small",
"bowel",
"or",
"ulcerative",
"colitis",
",",
"symptomatic",
"inflammatory",
"bowel",
"disease",
",",
"or",
"partial",
"or",
"complete",
"bowel",
"obstruction"
] |
[
2,
2,
0,
0,
0,
0,
2,
2,
0,
0,
2,
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2,
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2,
2,
2,
2,
2,
2,
0,
2,
2,
2,
2,
0,
0,
2,
2,
2,
2,
2
] |
NCT00809991
|
44:74:cancer
|
Histologically confirmed, locally confined adenocarcinoma of the prostate
| 3
|
[
"Histologically",
"confirmed",
",",
"locally",
"confined",
"adenocarcinoma",
"of",
"the",
"prostate"
] |
[
0,
0,
0,
0,
0,
3,
3,
3,
3
] |
NCT01853163
|
18:22:treatment
|
has received one GdCA injection at the standard dose
| 3
|
[
"has",
"received",
"one",
"GdCA",
"injection",
"at",
"the",
"standard",
"dose"
] |
[
0,
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT02494869
|
1:5:cancer
|
DCIS
| 3
|
[
"DCIS"
] |
[
3
] |
NCT02124772
|
41:44:cancer,48:51:cancer,52:58:cancer
|
Recurrent or refractory BRAFV600 mutant LGG or LCH tumors
| 3
|
[
"Recurrent",
"or",
"refractory",
"BRAFV600",
"mutant",
"LGG",
"or",
"LCH",
"tumors"
] |
[
0,
0,
0,
0,
0,
3,
0,
3,
3
] |
NCT02515773
|
70:102:chronic_disease
|
Diagnosed or told by a clinician that they have any of the following bipolar spectrum disorders (BSD)
| 3
|
[
"Diagnosed",
"or",
"told",
"by",
"a",
"clinician",
"that",
"they",
"have",
"any",
"of",
"the",
"following",
"bipolar",
"spectrum",
"disorders",
"(",
"BSD",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT01570998
|
1:5:cancer
|
HER2 positive (as defined in Treatment Policy under HER2)
| 3
|
[
"HER2",
"positive",
"(",
"as",
"defined",
"in",
"Treatment",
"Policy",
"under",
"HER2",
")"
] |
[
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02543866
|
1:19:chronic_disease
|
Bleeding diatheses
| 3
|
[
"Bleeding",
"diatheses"
] |
[
2,
2
] |
NCT02452008
|
23:32:chronic_disease,38:41:chronic_disease,43:54:chronic_disease,59:70:chronic_disease
|
Have known history of infection with HIV, hepatitis B, or hepatitis C
| 3
|
[
"Have",
"known",
"history",
"of",
"infection",
"with",
"HIV",
",",
"hepatitis",
"B",
",",
"or",
"hepatitis",
"C"
] |
[
0,
0,
0,
0,
2,
0,
2,
0,
2,
2,
0,
0,
0,
0
] |
NCT01696734
|
90:100:treatment
|
Patient has signed the informed consent document agreeing to the use of the study drug, domperidone
| 3
|
[
"Patient",
"has",
"signed",
"the",
"informed",
"consent",
"document",
"agreeing",
"to",
"the",
"use",
"of",
"the",
"study",
"drug",
",",
"domperidone"
] |
[
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1
] |
NCT01993810
|
1:16:chronic_disease,24:48:chronic_disease,59:74:treatment,
|
Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months
| 3
|
[
"Unstable",
"angina",
"and/or",
"congestive",
"heart",
"failure",
"requiring",
"hospitalization",
"within",
"the",
"last",
"6",
"months"
] |
[
2,
2,
0,
2,
2,
2,
0,
1,
0,
0,
0,
0,
0
] |
NCT03121586
|
1:11:treatment
|
Olanzapine
| 3
|
[
"Olanzapine"
] |
[
1
] |
NCT01473628
|
1:25:chronic_disease
|
Unstable angina pectoris
| 3
|
[
"Unstable",
"angina",
"pectoris"
] |
[
2,
2,
2
] |
NCT02269293
|
5:29:chronic_disease
|
Any life-threatening illness, medical condition or organ system dysfunction which, in the investigator's opinion, could compromise the subject's safety, or put the study outcomes at undue risk
| 3
|
[
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"life-threatening",
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0,
0,
0,
0,
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0
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NCT02338999
|
22:25:chronic_disease,,
|
Patients with severe SLE at baseline, as quantified as SLEDAI-2K >20
| 3
|
[
"Patients",
"with",
"severe",
"SLE",
"at",
"baseline",
",",
"as",
"quantified",
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0,
0,
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2,
0,
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0,
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0,
0,
0,
0,
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NCT02078102
|
30:73:treatment,
|
Patients must not have taken nonsteroidal antiinflammatory drugs (NSAID) in the past 14 days before treatment on this protocol
| 3
|
[
"Patients",
"must",
"not",
"have",
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"nonsteroidal",
"antiinflammatory",
"drugs",
"(",
"NSAID",
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02514083
|
12:34:treatment
|
history of bilateral oophorectomy
| 3
|
[
"history",
"of",
"bilateral",
"oophorectomy"
] |
[
0,
0,
1,
1
] |
NCT01555905
|
24:45:chronic_disease
|
Confirmed diagnosis of neuromuscular disease
| 3
|
[
"Confirmed",
"diagnosis",
"of",
"neuromuscular",
"disease"
] |
[
0,
0,
0,
2,
2
] |
NCT02498613
|
46:76:cancer,80:112:cancer,154:160:treatment
|
Patients may not have features suggestive of myelodysplastic syndrome (MDS) or acute myelogenous leukemia (AML) on peripheral blood smear or bone marrow biopsy
| 3
|
[
"Patients",
"may",
"not",
"have",
"features",
"suggestive",
"of",
"myelodysplastic",
"syndrome",
"(",
"MDS",
")",
"or",
"acute",
"myelogenous",
"leukemia",
"(",
"AML",
")",
"on",
"peripheral",
"blood",
"smear",
"or",
"bone",
"marrow",
"biopsy"
] |
[
0,
0,
0,
0,
0,
0,
0,
3,
3,
3,
0,
0,
0,
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT03171493
|
16:39:treatment
|
indication for Radical cystectomy (RC)
| 3
|
[
"indication",
"for",
"Radical",
"cystectomy",
"(",
"RC",
")"
] |
[
0,
0,
1,
1,
1,
0,
0
] |
NCT02938559
|
,65:68:treatment,69:71:treatment,76:86:chronic_disease
|
Lifetime history of failure to respond to 4 or more sessions of CBT/CT for depression
| 3
|
[
"Lifetime",
"history",
"of",
"failure",
"to",
"respond",
"to",
"4",
"or",
"more",
"sessions",
"of",
"CBT/CT",
"for",
"depression"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
2
] |
NCT01524536
|
27:39:treatment
|
Appropriate candidate for GC treatment after challenge
| 3
|
[
"Appropriate",
"candidate",
"for",
"GC",
"treatment",
"after",
"challenge"
] |
[
0,
0,
0,
1,
1,
0,
0
] |
NCT00887146
|
267:307:treatment
|
the 1p/19q analysis results will be accepted from the local site, as determined by either a locally available or reference laboratory (for US, must be Clinical Laboratory Improvement Act [CLIA] certified); acceptable methods for determination of 1p/19q loss include fluorescent in-situ hybridization (FISH), by genomic sequencing or methylomic analyses; US and Canadian sites must send a copy of the official report to the pathology coordinator and quality assurance specialist (QAS)
| 3
|
[
"the",
"1p/19q",
"analysis",
"results",
"will",
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"local",
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"as",
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"by",
"either",
"a",
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"reference",
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"(",
"for",
"US",
",",
"must",
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"CLIA",
"]",
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"acceptable",
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"(",
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",",
"by",
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"the",
"official",
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"and",
"quality",
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"(",
"QAS",
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0,
0,
0,
0,
0,
0,
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0,
0,
0,
0,
0,
0,
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0,
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02163317
|
8:19:treatment,
|
Use of finasteride within 30 days prior to registration
| 3
|
[
"Use",
"of",
"finasteride",
"within",
"30",
"days",
"prior",
"to",
"registration"
] |
[
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
NCT02664168
|
55:72:treatment
|
Subjects with a known history of poor compliance with medical treatment
| 3
|
[
"Subjects",
"with",
"a",
"known",
"history",
"of",
"poor",
"compliance",
"with",
"medical",
"treatment"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02397889
|
1:18:chronic_disease,,
|
hyroid impairment, as reflected by TSH> 4.2 mU/L
| 3
|
[
"hyroid",
"impairment",
",",
"as",
"reflected",
"by",
"TSH",
">",
"4.2",
"mU/L"
] |
[
2,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02057133
|
23:41:treatment,46:59:cancer,71:83:treatment,76:83:treatment,85:97:treatment,99:112:treatment,118:141:treatment,177:196:treatment,,223:246:treatment,,262:288:treatment,308:321:treatment,
|
Have discontinued all previous therapies for breast cancer (including chemotherapy, radiotherapy, immunotherapy, and investigational therapy), except for ongoing corresponding combination therapy, for at least 21 days for myelosuppressive agents or 14 days for nonmyelosuppressive agents prior to receiving study drug(s), and recovered from the acute effects of therapy (until the toxicity resolves to either baseline or at least Grade 1)
| 3
|
[
"Have",
"discontinued",
"all",
"previous",
"therapies",
"for",
"breast",
"cancer",
"(",
"including",
"chemotherapy",
",",
"radiotherapy",
",",
"immunotherapy",
",",
"and",
"investigational",
"therapy",
")",
",",
"except",
"for",
"ongoing",
"corresponding",
"combination",
"therapy",
",",
"for",
"at",
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"21",
"days",
"for",
"myelosuppressive",
"agents",
"or",
"14",
"days",
"for",
"nonmyelosuppressive",
"agents",
"prior",
"to",
"receiving",
"study",
"drug",
"(",
"s",
")",
",",
"and",
"recovered",
"from",
"the",
"acute",
"effects",
"of",
"therapy",
"(",
"until",
"the",
"toxicity",
"resolves",
"to",
"either",
"baseline",
"or",
"at",
"least",
"Grade",
"1",
")"
] |
[
0,
0,
0,
1,
1,
0,
3,
3,
0,
0,
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0,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02155699
|
26:40:chronic_disease
|
people who are extremely claustrophobic
| 3
|
[
"people",
"who",
"are",
"extremely",
"claustrophobic"
] |
[
0,
0,
0,
0,
2
] |
NCT00959140
|
1:4:cancer,20:29:treatment,34:49:treatment
|
AML: Refractory to Induction and salvage therapy
| 3
|
[
"AML",
":",
"Refractory",
"to",
"Induction",
"and",
"salvage",
"therapy"
] |
[
3,
0,
0,
0,
1,
0,
1,
1
] |
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