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NCT01795573
|
77:80:treatment,77:94:cancer,77:95:cancer,104:113:treatment,263:265:treatment,321:352:treatment,334:352:treatment,445:465:treatment
|
NHL: No clinical evidence of disease or disease-related symptoms; Typically FDG-avid lymphomas: a post-treatment residual mass of any size is permitted as long as it is PET negative; Variably FDG-avid lymphoma/FDG avidity unknown: all lymph nodes normal size by CT; Spleen and liver non-palpable and without nodules; If pretreatment bone marrow biopsy was positive, repeat bone marrow biopsy must be negative; if morphologically indeterminate, immunohistochemistry should be negative If pretreatment bone marrow biopsy was positive, repeat bone marrow biopsy must be negative; if morphologically indeterminate, immunohistochemistry should be negative
| 1
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NCT01553942
|
7:23:treatment
|
Prior EGFR TKI therapy
| 1
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NCT03078153
|
1:4:chronic_disease
|
HIV negative
| 1
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"HIV",
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NCT02128100
|
71:81:cancer
|
A reasonable attempt should be made to make a pathologic diagnosis of malignancy
| 1
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NCT02762266
|
11:41:cancer
|
Confirmed hepatocellular carcinoma (HCC)
| 1
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NCT01827384
|
15:24:treatment,33:69:cancer,57:60:cancer,70:100:cancer,96:99:cancer,158:197:treatment,201:244:treatment
|
Patients with treatment-related acute myeloid leukemia (AML) (t-AML)/myelodysplastic syndrome (MDS), or with features suggestive of AML/MDS, or who have had prior allogeneic bone marrow transplant or double umbilical cord blood transplantation
| 1
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NCT01174108
|
,,110:114:treatment
|
ECOG performance status of 3 or more (See Bone & Marrow Transplant Consortium Supportive Care Guidelines for HSCT Recipients)
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NCT00911560
|
,,178:190:treatment
|
stage 4 with (any age) or without (>18 months old) MYCN amplification, MYCN-amplified stage 3 (unresectable; any age), MYCN-amplified stage 4S, or disease resistant to standard chemotherapy
| 1
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NCT02982564
|
18:31:cancer,,
|
Be classified in breast cancer stage grouping 0 to III according to the American Joint Committee on Cancer Classification of Malignant Tumors (TNM) Staging System (2013)
| 1
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NCT02109627
|
,,67:79:treatment,129:139:treatment,,187:198:treatment
|
Pregnant women are excluded from this study because the effect of ficlatuzumab on the developing fetus remains unknown and that cytarabine is a pregnancy risk category D drug with known teratogenic or abortifacient effects
| 1
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NCT00904046
|
1:7:chronic_disease
|
Anemia
| 1
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NCT02495935
|
15:24:treatment,80:97:chronic_disease,108:127:chronic_disease,129:142:chronic_disease
|
Presence of a pacemaker, any metal artifacts in head and trunk, any history of epileptic seizure or severe psychiatric disease (schizophrenia, etc.)
| 1
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NCT03058029
|
12:28:chronic_disease,,,,
|
History of eating disorders including binge eating (except for mild binge eating)or emesis ≥2/week from any cause Weight change >3% within three(3) months prior to and during the Screening period
| 1
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NCT02465060
|
50:84:treatment
|
Registration to Step 0 must occur after stopping prior systemic anti-cancer therapy
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NCT02502006
|
6:35:treatment,17:35:treatment,47:58:treatment,60:69:treatment,71:79:treatment,
|
Used dietary or herbal supplements containing salicylates, Vitamin E, fish oil, or any other herbal supplements, within 14 days of study drug administration
| 1
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NCT02148003
|
53:69:allergy_name
|
Subjects who have a history of adverse reactions to local anesthetic
| 1
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NCT02600897
|
1:25:treatment,31:39:cancer,47:81:treatment
|
fluorodeoxyglucose (FDG)-avid lymphoma (i.e., positron emission tomography (PET)-positive lymphoma)
| 1
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NCT03075826
|
43:53:cancer
|
Individuals with a history of a different malignancy
| 1
|
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NCT02759211
|
42:57:chronic_disease,59:92:chronic_disease,111:145:chronic_disease,147:185:chronic_disease,187:210:chronic_disease,214:234:chronic_disease,247:250:chronic_disease,252:269:chronic_disease,273:285:chronic_disease,287:311:chronic_disease,313:338:chronic_disease,344:365:chronic_disease
|
Current self-reported medical history of unstable angina, uncontrolled cardiac dysrhythmias causing symptoms, symptomatic severe aortic stenosis, uncontrolled symptomatic heart failure, acute pulmonary embolus or pulmonary infarction, history of DVT, acute myocarditis or pericarditis, acute systemic infection, uncontrolled hypertension, and uncontrolled diabetes [11]
| 1
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NCT01827384
|
15:42:chronic_disease,138:153:treatment,192:217:treatment,240:262:chronic_disease,268:295:chronic_disease
|
Patients with gastrointestinal conditions that might predispose for drug intolerability or poor drug absorption (e.g., inability to take oral medication or a requirement for IV alimentation, prior surgical procedures affecting absorption, malabsorption syndrome, and active peptic ulcer disease)
| 1
|
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NCT02112565
|
,,,,,,101:117:cancer
|
Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) =< 2.5 x ULN; AST/ALT =< 5 x ULN if liver metastasis is present
| 1
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NCT02110069
|
1:15:cancer
|
Tufted angioma
| 1
|
[
"Tufted",
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[
3,
3
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NCT01756040
|
1:32:chronic_disease
|
Lethal chromosome abnormalities
| 1
|
[
"Lethal",
"chromosome",
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[
2,
2,
2
] |
NCT02503722
|
31:53:treatment,57:69:treatment,71:93:treatment,129:143:treatment
|
Documentation of irreversible surgical sterilization by hysterectomy, bilateral oophorectomy or bilateral salpingectomy but not tubal ligation
| 1
|
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NCT02403193
|
108:117:treatment
|
Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up
| 1
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NCT01986075
|
19:22:chronic_disease,,105:132:chronic_disease,302:317:treatment,321:334:treatment
|
Participants with MDD, with symptom severity that exceeds a HAM-D score of 20, and/or any other current Axis I psychiatric disorder as defined by DSM-V supported by the MINI that in the investigator's judgment are unstable, would be disrupted by study medication, or are likely to require specialized pharmacotherapy or psychotherapy during the study period
| 1
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NCT02983240
|
1:32:chronic_disease,,
|
Severe fetal growth restriction (EFW < 5%)
| 1
|
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NCT02531932
|
28:66:treatment,68:77:treatment,79:91:treatment,93:103:treatment
|
Patients who have received prior treatment with an mTOR inhibitor (sirolimus, temsirolimus, everolimus)
| 1
|
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NCT02393690
|
77:93:chronic_disease,95:116:chronic_disease,118:139:chronic_disease,153:177:chronic_disease,179:203:chronic_disease,205:223:chronic_disease,228:265:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, hepatitis B infection, hepatitis C infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
| 1
|
[
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NCT01530958
|
1:18:treatment
|
Kidney transplant recipients
| 1
|
[
"Kidney",
"transplant",
"recipients"
] |
[
1,
1,
0
] |
NCT02903446
|
1:21:chronic_disease,,,
|
Vitamin D deficiency [25(OH) vitamin D level < 20 ng/mL (<49.9 nmol/L)]†
| 1
|
[
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0
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NCT02358187
|
4:17:chronic_disease,19:35:chronic_disease,37:46:chronic_disease,50:69:chronic_disease
|
No overt cardiac, gastrointestinal, pulmonary or psychiatric disease
| 1
|
[
"No",
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",",
"gastrointestinal",
",",
"pulmonary",
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[
0,
2,
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0,
2,
0,
2,
0,
2,
2
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NCT02427581
|
25:38:cancer,
|
Evidence of progressive breast cancer within the last 30 days
| 1
|
[
"Evidence",
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"breast",
"cancer",
"within",
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"30",
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0,
0,
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3,
3,
0,
0,
0,
0,
0
] |
NCT02312518
|
18:48:treatment,,87:96:treatment,98:107:treatment,111:120:treatment
|
Received another investigational device or drug within 30 days of enrollment Received allograft, autograft or xenograft within 30 days of enrollment
| 1
|
[
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"30",
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0,
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NCT01841333
|
1:18:treatment
|
azole antifungals
| 1
|
[
"azole",
"antifungals"
] |
[
1,
1
] |
NCT02106988
|
1:16:treatment,7:16:treatment,60:72:treatment
|
Prior radiation to the site of current primary disease, if re-treatment would lead to violation of known radiation dose tolerance limits for that site
| 1
|
[
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NCT02469519
|
46:61:treatment
|
Any contraindications to the maternal use of corticosteroids
| 1
|
[
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[
0,
0,
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0,
0,
0,
1
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NCT01959698
|
,,,31:36:cancer
|
Ann Arbor stage I to stage IV DLBCL at the time of relapsed/refractory disease to be eligible
| 1
|
[
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NCT01444209
|
45:80:cancer
|
Pathological or radiographic diagnosis of a pan-invasive pituitary macroadenoma
| 1
|
[
"Pathological",
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"radiographic",
"diagnosis",
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"macroadenoma"
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[
0,
0,
0,
0,
0,
0,
3,
3,
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NCT02581215
|
57:83:treatment,87:102:treatment,110:118:treatment,122:133:treatment
|
Subjects whose disease has progressed after 6 months of last systemic chemotherapy or chemo-radiation in the adjuvant or neoadjuvant setting
| 1
|
[
"Subjects",
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"has",
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"chemo-radiation",
"in",
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NCT02059239
|
,,,,95:98:treatment
|
Partial response of >50% reduction in bidirectional area of masses and SUV reduction to <8 in PET avid areas Subjects must have evaluable disease
| 1
|
[
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"50",
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NCT02095184
|
37:55:treatment,57:74:treatment,79:96:treatment,115:128:cancer
|
Patients must not have received any prior chemotherapy, radiation therapy, or endocrine therapy for their current breast cancer
| 1
|
[
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NCT02304458
|
35:50:treatment
|
Patients requiring daily systemic corticosteroids
| 1
|
[
"Patients",
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"daily",
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"corticosteroids"
] |
[
0,
0,
0,
0,
1
] |
NCT02465060
|
5:18:treatment,20:32:treatment,41:69:treatment,,99:112:treatment,,167:176:treatment
|
Any prior therapy, radiotherapy (except palliative radiation therapy of 30 gray [Gy] or less), or major surgery must have been completed >= 4 weeks prior to start of treatment
| 1
|
[
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NCT02332850
|
24:34:treatment
|
inability to take oral medication
| 1
|
[
"inability",
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"oral",
"medication"
] |
[
0,
0,
0,
0,
1
] |
NCT02734134
|
1:18:chronic_disease
|
Fungal infections
| 1
|
[
"Fungal",
"infections"
] |
[
2,
2
] |
NCT02474667
|
,43:67:treatment
|
Must have a negative serum pregnancy test prior to transplantation
| 1
|
[
"Must",
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"a",
"negative",
"serum",
"pregnancy",
"test",
"prior",
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"transplantation"
] |
[
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT01465100
|
13:19:chronic_disease,21:30:chronic_disease,38:54:chronic_disease
|
Subject has sepsis, pneumonia, other active infection
| 1
|
[
"Subject",
"has",
"sepsis",
",",
"pneumonia",
",",
"other",
"active",
"infection"
] |
[
0,
0,
2,
0,
2,
0,
0,
2,
2
] |
NCT02533674
|
7:51:chronic_disease
|
Known human immunodeficiency virus (HIV) infection
| 1
|
[
"Known",
"human",
"immunodeficiency",
"virus",
"(",
"HIV",
")",
"infection"
] |
[
0,
2,
2,
2,
2,
2,
0,
0
] |
NCT02146924
|
36:51:treatment
|
Research participant has undergone lymphodepletion
| 1
|
[
"Research",
"participant",
"has",
"undergone",
"lymphodepletion"
] |
[
0,
0,
0,
0,
1
] |
NCT00412594
|
13:29:chronic_disease
|
Presence of active infection
| 1
|
[
"Presence",
"of",
"active",
"infection"
] |
[
0,
0,
2,
2
] |
NCT02566304
|
28:39:treatment,43:65:treatment,,88:98:treatment,131:140:treatment
|
Patients who have received alemtuzumab or antithymocyte globulin within 8 weeks of the transplant admission. The absence of these therapies in the medical record will serve as documentation that they were not given
| 1
|
[
"Patients",
"who",
"have",
"received",
"alemtuzumab",
"or",
"antithymocyte",
"globulin",
"within",
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"weeks",
"of",
"the",
"transplant",
"admission",
".",
"The",
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"of",
"these",
"therapies",
"in",
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"medical",
"record",
"will",
"serve",
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[
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0,
0,
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0,
0,
0,
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] |
NCT02050347
|
5:13:cancer,102:116:treatment,122:148:treatment
|
Any leukemia specific marker (such as t(9:22) or t(4:11)) documented in the patient's leukemia cells pre transplant on a post transplant evaluation
| 1
|
[
"Any",
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[
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1,
1,
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0,
1,
1,
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NCT02181478
|
6:15:treatment
|
such treatment may continue until the planned course is completed
| 1
|
[
"such",
"treatment",
"may",
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"until",
"the",
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"course",
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[
0,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02019641
|
16:41:chronic_disease,53:88:chronic_disease,90:134:chronic_disease,136:147:chronic_disease,166:187:chronic_disease
|
A diagnosis of interstitial lung disease, including idiopathic pulmonary fibrosis (IPF), non-specific interstitial pneumonitis (NSIP), sarcoidosis, or other form of chronic lung fibrosis based on clinical context via clinic note from a pulmonologist
| 1
|
[
"A",
"diagnosis",
"of",
"interstitial",
"lung",
"disease",
",",
"including",
"idiopathic",
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"fibrosis",
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"IPF",
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",",
"non-specific",
"interstitial",
"pneumonitis",
"(",
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",",
"sarcoidosis",
",",
"or",
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"form",
"of",
"chronic",
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"based",
"on",
"clinical",
"context",
"via",
"clinic",
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"from",
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[
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02988960
|
57:75:chronic_disease,
|
Participant must not have an active or prior documented autoimmune disease in the last 2 years
| 1
|
[
"Participant",
"must",
"not",
"have",
"an",
"active",
"or",
"prior",
"documented",
"autoimmune",
"disease",
"in",
"the",
"last",
"2",
"years"
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
0,
0,
0
] |
NCT02177695
|
37:39:treatment,43:51:treatment,56:63:treatment,67:72:treatment,
|
Staging scans with abdominal/pelvic CT or MRI scan and CT scan or x-ray of the chest within 56 days prior to registration
| 1
|
[
"Staging",
"scans",
"with",
"abdominal/pelvic",
"CT",
"or",
"MRI",
"scan",
"and",
"CT",
"scan",
"or",
"x-ray",
"of",
"the",
"chest",
"within",
"56",
"days",
"prior",
"to",
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[
0,
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0,
0,
0,
0,
0,
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] |
NCT00703105
|
59:84:cancer
|
Patients must have a histologic or cytologic diagnosis of epithelial ovarian cancer
| 1
|
[
"Patients",
"must",
"have",
"a",
"histologic",
"or",
"cytologic",
"diagnosis",
"of",
"epithelial",
"ovarian",
"cancer"
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
3
] |
NCT02219555
|
81:89:chronic_disease
|
someone who could be considered a vulnerable person, such as an individual with dementia
| 1
|
[
"someone",
"who",
"could",
"be",
"considered",
"a",
"vulnerable",
"person",
",",
"such",
"as",
"an",
"individual",
"with",
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
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] |
NCT02583893
|
1:10:treatment,18:26:treatment,28:35:treatment,37:44:treatment
|
Verapamil (e.g., Calan SR, Isoptin, Verelan)
| 1
|
[
"Verapamil",
"(",
"e.g.",
",",
"Calan",
"SR",
",",
"Isoptin",
",",
"Verelan",
")"
] |
[
1,
0,
0,
0,
1,
1,
0,
1,
0,
1,
0
] |
NCT02332928
|
,67:76:treatment,
|
willing to use an acceptable method of birth control during study treatment and for 3 months afterwards
| 1
|
[
"willing",
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"use",
"an",
"acceptable",
"method",
"of",
"birth",
"control",
"during",
"study",
"treatment",
"and",
"for",
"3",
"months",
"afterwards"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
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0,
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0
] |
NCT02596776
|
1:25:chronic_disease
|
congestive heart failure
| 1
|
[
"congestive",
"heart",
"failure"
] |
[
2,
2,
2
] |
NCT02454010
|
14:48:chronic_disease,50:91:chronic_disease,95:118:chronic_disease
|
positive for human immunodeficiency virus (HIV), hepatitis B virus surface antigen (HBsAg) or hepatitis C virus (HCV)
| 1
|
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NCT02632721
|
33:69:treatment
|
Patients who are candidates for allogeneic stem cell transplantation
| 1
|
[
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1,
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NCT01787409
|
61:70:treatment
|
During the Active Monitoring Phase of a study (i.e., active treatment and observation), participants must be willing to return to the consenting institution for follow-up
| 1
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NCT01676259
|
1:18:chronic_disease
|
hepatitis B virus
| 1
|
[
"hepatitis",
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"virus"
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[
2,
2,
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NCT03105362
|
1:25:chronic_disease
|
epithelial cell disorder
| 1
|
[
"epithelial",
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"disorder"
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[
2,
2,
2
] |
NCT01494662
|
1:21:chronic_disease,27:47:chronic_disease,51:73:chronic_disease
|
Active liver disease from autoimmune disorders or sclerosing cholangitis
| 1
|
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NCT02181478
|
1:33:cancer
|
Acute myelogenous leukemia (AML)
| 1
|
[
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[
3,
3,
3,
3,
0,
0
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NCT01959204
|
10:20:treatment,60:66:treatment,,110:133:treatment,134:146:treatment,151:163:treatment,165:186:treatment,195:207:treatment,213:232:treatment,241:250:treatment,285:293:treatment,295:308:treatment,314:323:treatment
|
Uses any medication known to be an inhibitor or inducer of CYP3A4 within 14 days (for inhibitors such as the azole-antifungal agents voriconazole and ketoconazole, macrolide antibiotics such as erythromycin, and protease inhibitors such as ritonavir) or 28 days (for inducers such as rifampin, carbamazepine, and phenytoin) of dosing with study drug
| 1
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NCT02567227
|
5:22:chronic_disease,26:44:treatment,56:68:treatment,133:149:chronic_disease,,
|
Any medical condition or chronic medication use (e.g., neuroleptics) that will compromise safety or affect cognitive functioning or terminal illness with life expectancy less than 12 months
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NCT02723266
|
13:16:chronic_disease,33:51:chronic_disease,53:65:chronic_disease,,,,
|
at risk for GDM (such as having metabolic syndrome, pre-diabetes, or BMI > 85%; and an A1C < 6.5%)
| 1
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NCT02496208
|
,,75:87:chronic_disease
|
Lipase and amylase =< 2.0 x ULN and no radiologic or clinical evidence of pancreatitis
| 1
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NCT02759146
|
12:24:treatment
|
Undergoing chemotherapy
| 1
|
[
"Undergoing",
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] |
[
0,
1
] |
NCT02816736
|
8:25:chronic_disease,
|
Severe liver dysfunction (Childs-Pugh Class C)
| 1
|
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NCT03170349
|
19:22:treatment
|
Patient in whom a TEE is contraindicated or screening TEE is unsuccessful
| 1
|
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0,
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0,
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0
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NCT02453373
|
1:25:chronic_disease
|
Ventricular fibrillation
| 1
|
[
"Ventricular",
"fibrillation"
] |
[
2,
2
] |
NCT01430390
|
,,,51:75:chronic_disease
|
New York Heart Association (NYHA) stage III or IV congestive heart failure
| 1
|
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NCT02811679
|
1:38:chronic_disease
|
psychiatric illness/social situations that would limit compliance with study requirements
| 1
|
[
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2,
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0,
0,
0,
0,
0,
0,
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] |
NCT02057133
|
46:83:treatment
|
For Parts A, B, C, D, E, F, H: Have received prior therapy with a CDK4/6 inhibitor
| 1
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NCT00977977
|
53:75:treatment,115:123:chronic_disease,125:142:chronic_disease,146:158:chronic_disease
|
evidence of intolerance or toxicity associated with cyclosporine treatment of any duration including irreversible azotemia, liver dysfunction or hypertension
| 1
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NCT02527421
|
1:13:treatment
|
PUVA therapy
| 1
|
[
"PUVA",
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] |
[
1,
1
] |
NCT02169739
|
7:15:chronic_disease,19:33:chronic_disease,69:81:treatment
|
Prior cortical or retinal stroke (diagnosed either clinically or by neuroimaging)
| 1
|
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NCT02343042
|
1:10:treatment,12:24:treatment,29:42:treatment,56:74:treatment,,94:98:treatment,104:123:treatment,
|
Radiation, chemotherapy, or immunotherapy or any other anticancer therapy ≤ 2 weeks prior to C1D1, and radio-immunotherapy within 6 weeks prior to C1D1
| 1
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NCT02424968
|
7:17:cancer
|
Prior malignancy
| 1
|
[
"Prior",
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] |
[
0,
3
] |
NCT02931110
|
1:29:treatment
|
low-molecular-weight heparin
| 1
|
[
"low-molecular-weight",
"heparin"
] |
[
1,
1
] |
NCT03088072
|
1:37:treatment
|
LAA closure with the WATCHMAN device is planned
| 1
|
[
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[
1,
1,
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1,
1,
1,
0,
0
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NCT02366481
|
28:31:allergy_name
|
Subjects with a history of soy allergy
| 1
|
[
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[
0,
0,
0,
0,
0,
4,
0
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NCT02523443
|
21:38:allergy_name,59:77:chronic_disease,79:104:chronic_disease,106:141:chronic_disease,143:165:chronic_disease,171:188:chronic_disease,191:215:chronic_disease,217:235:chronic_disease,237:268:chronic_disease,272:315:chronic_disease,318:348:treatment,352:374:chronic_disease,397:411:treatment,499:525:chronic_disease,,,,,,,
|
Contraindication to epidural catheter placement including bleeding diathesis (essential thrombocythemia, idiopathic thrombocytopenic purpura, von Willebrand disease, and hemophilia A or B), neurological dysfunction (multiple sclerosis, subacute myelo-opticoneuropathy or preexisting lower limb neurological deficit), prior extensive spinal surgery or major spinal deformity, pre-operative use of anti-coagulant with planned use of therapeutic dose of anti-coagulant in post-operatively, documented pre-operative coagulopathy (INR greater than 1.3 not on Coumadin or PTT greater than 42), platelets less than 100,000/μL, or evidence of infection at potential epidural site
| 1
|
[
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NCT00788164
|
1:27:chronic_disease
|
Human papillomavirus (HPV) 16-positive disease by PCR
| 1
|
[
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[
2,
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT03088033
|
,,53:55:chronic_disease
|
Tricuspid valve regurgitation defined as grade > 2+ TR
| 1
|
[
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"regurgitation",
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[
0,
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT02564796
|
26:40:chronic_disease
|
Infants with significant co-morbidities
| 1
|
[
"Infants",
"with",
"significant",
"co-morbidities"
] |
[
0,
0,
0,
2
] |
NCT02263274
|
17:39:chronic_disease,50:61:cancer,63:88:chronic_disease,90:112:chronic_disease,114:138:treatment,154:169:chronic_disease
|
Space occupying intracranial pathology including brain tumor, ateriovenous malformation, cavernous malformation, prior surgical resection or significant encephalomalcia that would create unknown tissue inhomogeneity that cannot be accurately modeled
| 1
|
[
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"that",
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0,
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NCT03077243
|
1:7:treatment,15:38:cancer,47:50:chronic_disease
|
Biopsy proven squamous cell carcinoma that is HPV and/or p16 positive
| 1
|
[
"Biopsy",
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"carcinoma",
"that",
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[
1,
0,
3,
3,
3,
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0,
0
] |
NCT03049189
|
27:31:allergy_name,33:45:allergy_name,54:78:allergy_name,82:92:allergy_name,96:126:allergy_name
|
Known hypersensitivity to DOTA, lutetium-177, or any excipient of edotreotide or everolimus or any other Rapamycin derivative
| 1
|
[
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0,
0
] |
NCT02516813
|
104:115:treatment,119:137:treatment,171:186:treatment,187:194:treatment,198:205:treatment,,260:265:treatment,,344:381:treatment,
|
Subjects currently receiving (or unable to stop using prior to receiving the first dose of trial drug) medications or herbal supplements known to be potent inhibitors of cytochrome P450 (CYP)3A or CYP2C19 (must stop at least 1 week prior), potent inducers of CYP3A or CYP2C19 (must stop at least 3 weeks prior), or drugs mainly metabolized by CYP3A with a narrow therapeutic index (must stop at least one day prior)
| 1
|
[
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[
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] |
NCT01595529
|
1:11:chronic_disease
|
flank pain
| 1
|
[
"flank",
"pain"
] |
[
2,
2
] |
NCT01666665
|
35:48:chronic_disease
|
Previous diagnosis (pre -burn) of renal failure
| 1
|
[
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[
0,
0,
0,
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0,
0,
2,
2
] |
NCT02349867
|
,,,121:130:treatment
|
Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment
| 1
|
[
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0,
0,
0,
1
] |
NCT02427841
|
4:17:treatment,22:39:cancer,51:63:treatment,65:82:treatment,95:102:treatment,106:129:treatment
|
No prior therapy for pancreatic cancer, including chemotherapy, radiation therapy, definitive surgery or investigational therapy
| 1
|
[
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1
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