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1.5k
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list | ner_tags
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NCT01919619
|
1:12:chronic_disease
|
hepatitis B
| 1
|
[
"hepatitis",
"B"
] |
[
2,
2
] |
NCT02581215
|
12:28:chronic_disease
|
Ongoing or active infection
| 1
|
[
"Ongoing",
"or",
"active",
"infection"
] |
[
0,
0,
2,
2
] |
NCT02553161
|
26:50:chronic_disease,69:74:chronic_disease,76:89:chronic_disease,94:110:chronic_disease,116:125:chronic_disease
|
any history of syndromal bipolar I or II disorder (i.e., history of mania, mixed episode, or major depression with hypomania)
| 1
|
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NCT01389024
|
1:11:chronic_disease
|
Cytopenias
| 1
|
[
"Cytopenias"
] |
[
2
] |
NCT02646930
|
10:37:treatment
|
previous uterine artery embolization
| 1
|
[
"previous",
"uterine",
"artery",
"embolization"
] |
[
0,
1,
1,
1
] |
NCT02016781
|
1:45:chronic_disease
|
Human Immunodeficiency Virus (HIV) infection
| 1
|
[
"Human",
"Immunodeficiency",
"Virus",
"(",
"HIV",
")",
"infection"
] |
[
2,
2,
2,
2,
2,
0,
0
] |
NCT02323100
|
1:14:treatment,
|
Sinus surgery within 6 weeks of Screening Visit
| 1
|
[
"Sinus",
"surgery",
"within",
"6",
"weeks",
"of",
"Screening",
"Visit"
] |
[
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT02567227
|
1:9:chronic_disease
|
dementia diagnosed by baseline cognitive assessment
| 1
|
[
"dementia",
"diagnosed",
"by",
"baseline",
"cognitive",
"assessment"
] |
[
2,
0,
0,
0,
0,
0
] |
NCT02496611
|
36:63:cancer
|
Personal- and/or family history of medullary thyroid carcinoma
| 1
|
[
"Personal-",
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"family",
"history",
"of",
"medullary",
"thyroid",
"carcinoma"
] |
[
0,
0,
0,
0,
0,
3,
3,
3
] |
NCT01841333
|
,,24:44:treatment
|
Between days 28 and 50 post transplantation at the time of initiation of the study drug
| 1
|
[
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NCT02430077
|
13:37:cancer,,,94:104:chronic_disease,136:148:cancer
|
Evidence of hepatocellular carcinoma: alpha-fetoprotein levels greater than 200 ng/ml and/or liver mass on imaging study suggestive of liver cancer
| 1
|
[
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NCT01953263
|
15:35:chronic_disease
|
Patients with urinary incontinence other than the categories being investigated
| 1
|
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0,
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0,
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NCT02451488
|
1:29:treatment,31:39:treatment,41:79:treatment,81:93:treatment,
|
Immunosuppressive mediations (steroids, tumor necrosis factor (TNF)-inhibitors, azathioprine, etc.) within the past 6 weeks
| 1
|
[
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NCT02359864
|
36:58:treatment
|
Patient currently participating in another Clinical Trial
| 1
|
[
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NCT02986815
|
23:47:chronic_disease
|
NYHA class III and IV congestive heart failure
| 1
|
[
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[
0,
0,
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0,
2,
2,
2
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NCT02107261
|
35:43:chronic_disease
|
Patients with focal task-specific dystonia of one or both hands
| 1
|
[
"Patients",
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"task-specific",
"dystonia",
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0,
0,
0,
0,
2,
0,
0,
0,
0,
0
] |
NCT03035890
|
12:28:chronic_disease
|
ongoing or active infection
| 1
|
[
"ongoing",
"or",
"active",
"infection"
] |
[
0,
0,
2,
2
] |
NCT02639390
|
1:31:chronic_disease,
|
Ischemic or hemorrhagic stroke (with confirmatory neuroimaging) that occurred more than 6 months before entering the study
| 1
|
[
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NCT02990377
|
,26:47:treatment
|
Past 3-month non-medical opioid analgesic (OA) use
| 1
|
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NCT02556606
|
85:104:treatment
|
Past intolerance or hypersensitivity to ketamine, or history of recreational use of phencyclidine (PCP) or ketamine
| 1
|
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NCT02361554
|
28:46:chronic_disease
|
Subject has a diagnosis of mental retardation
| 1
|
[
"Subject",
"has",
"a",
"diagnosis",
"of",
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] |
[
0,
0,
0,
0,
0,
2,
2
] |
NCT02501473
|
41:49:cancer,61:72:cancer,77:99:cancer
|
Central nervous system involvement with lymphoma, including parenchymal and leptomeningeal disease
| 1
|
[
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"system",
"involvement",
"with",
"lymphoma",
",",
"including",
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0,
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0,
0,
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3,
0,
3,
3
] |
NCT02780401
|
59:68:treatment,
|
History of autoimmunity that has not been controlled with treatment in the last 12 months
| 1
|
[
"History",
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"autoimmunity",
"that",
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"not",
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NCT02874898
|
18:42:treatment,
|
Unstable dose of psychotropic medications in the prior 3 months
| 1
|
[
"Unstable",
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"of",
"psychotropic",
"medications",
"in",
"the",
"prior",
"3",
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] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0
] |
NCT02030015
|
33:77:chronic_disease
|
Subjects must have a documented infantile or juvenile gangliosidosis disease
| 1
|
[
"Subjects",
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"a",
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2,
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NCT02496208
|
1:16:treatment,22:33:treatment,26:33:treatment,176:196:cancer
|
Prior treatment with any therapy on the programmed cell death 1 (PD-1)/PD-L1 axis or anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors unless enrolling the urothelial carcinoma with previous checkpoint inhibition therapy expansion cohort
| 1
|
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NCT01905046
|
14:24:cancer,
|
Other active malignancy =< 5 years prior to pre-registration
| 1
|
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NCT02674984
|
1:26:chronic_disease,35:49:chronic_disease,51:77:chronic_disease
|
Gastrointestinal diseases such as celiac disease, inflammatory bowel disease
| 1
|
[
"Gastrointestinal",
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"celiac",
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",",
"inflammatory",
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2,
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0,
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2,
2
] |
NCT02393885
|
1:43:chronic_disease,47:101:chronic_disease,143:147:treatment
|
Symptomatic Persistent Atrial Fibrillation or Longstanding Persistent Atrial Fibrillation refractory to a minimum of one Class I or Class III AADs
| 1
|
[
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NCT02519946
|
1:14:chronic_disease
|
Acute illness
| 1
|
[
"Acute",
"illness"
] |
[
2,
2
] |
NCT01937884
|
4:46:treatment
|
On extracorporeal membrane oxygenation (ECMO)
| 1
|
[
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"oxygenation",
"(",
"ECMO",
")"
] |
[
0,
1,
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1,
0,
0
] |
NCT02133573
|
30:41:treatment,65:77:treatment,84:97:treatment,99:108:treatment,110:122:treatment,126:137:treatment
|
Prescription or ingestion of medications known to interact with progesterone (e.g. Bromocriptine, Rifamycin, Ketoconazole or Cyclosporin)
| 1
|
[
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NCT01690468
|
31:43:treatment
|
At least one prior regimen of chemotherapy, with no maximum number of chemotherapy cycles
| 1
|
[
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NCT02512926
|
1:9:cancer
|
Lymphoma patients are permitted
| 1
|
[
"Lymphoma",
"patients",
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] |
[
3,
0,
0,
0
] |
NCT02132598
|
72:117:allergy_name
|
The subject has a previously identified allergy or hypersensitivity to components of the study treatment formulation
| 1
|
[
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NCT02459119
|
15:25:chronic_disease,27:34:chronic_disease,36:42:chronic_disease,47:62:chronic_disease,72:96:chronic_disease,108:134:chronic_disease,136:156:chronic_disease,160:178:chronic_disease,,213:222:treatment
|
Subjects with thrombotic, embolic, venous, or arterial events, such as cerebrovascular accident (including transient ischemic attacks) deep vein thrombosis or pulmonary embolism within 6 months of start of study treatment within 6 months of informed consent
| 1
|
[
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NCT02862938
|
19:31:treatment
|
Participant is on chemotherapy
| 1
|
[
"Participant",
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[
0,
0,
0,
1
] |
NCT03058796
|
1:30:chronic_disease
|
uncontrolled seizure disorder
| 1
|
[
"uncontrolled",
"seizure",
"disorder"
] |
[
2,
2,
2
] |
NCT02143830
|
1:27:cancer
|
Acute Myelogenous Leukemia (untreated, in remission or with refractory or relapsed disease)
| 1
|
[
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[
3,
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0,
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0
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NCT02541903
|
1:17:chronic_disease
|
chronic diarrhea
| 1
|
[
"chronic",
"diarrhea"
] |
[
2,
2
] |
NCT02080221
|
13:23:chronic_disease
|
Preexisting neuropathy
| 1
|
[
"Preexisting",
"neuropathy"
] |
[
0,
2
] |
NCT02135874
|
23:46:chronic_disease
|
Patients with active, uncontrolled infections
| 1
|
[
"Patients",
"with",
"active",
",",
"uncontrolled",
"infections"
] |
[
0,
0,
0,
0,
2,
2
] |
NCT02332291
|
1:35:chronic_disease
|
generalized anxiety disorder (GAD) symptoms occurring during a depressive episode
| 1
|
[
"generalized",
"anxiety",
"disorder",
"(",
"GAD",
")",
"symptoms",
"occurring",
"during",
"a",
"depressive",
"episode"
] |
[
2,
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2,
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0,
0,
0,
0,
0,
0,
0
] |
NCT01624090
|
1:8:treatment
|
Dextran
| 1
|
[
"Dextran"
] |
[
1
] |
NCT02377089
|
23:37:treatment,39:50:treatment,52:65:treatment,70:96:treatment,
|
evidence of receiving antidepressant, antianxiety, antipsychotic, or mood-stabilizer medication where the dose has not been stable for a minimum of six weeks prior to entering the randomization
| 1
|
[
"evidence",
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NCT02135588
|
17:34:cancer
|
Presence of any intracranial mass
| 1
|
[
"Presence",
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"any",
"intracranial",
"mass"
] |
[
0,
0,
0,
3,
3
] |
NCT01261728
|
43:76:cancer,142:147:cancer,201:217:treatment
|
Histologically confirmed high-grade upper tract transitional cell carcinoma at MSKCC or a participating site and/or radiographically visible tumor stage T2-T4a N0/X M0 disease with positive selective urinary cytology or high-grade concomitant bladder tumor
| 1
|
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NCT02273362
|
3:24:treatment,
|
A clinical liver biopsy (with research tissue specimens available for analysis) =< 3 months prior to pre-registration
| 1
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NCT01925131
|
30:64:chronic_disease,
|
Patients who are known to be human immunodeficiency virus (HIV)+ are eligible providing they meet all of the following additional criteria within 28 days prior to registration
| 1
|
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NCT02203903
|
1:24:chronic_disease
|
Uncontrolled infections
| 1
|
[
"Uncontrolled",
"infections"
] |
[
2,
2
] |
NCT01811368
|
14:38:chronic_disease
|
uncontrolled congestive heart failure
| 1
|
[
"uncontrolled",
"congestive",
"heart",
"failure"
] |
[
0,
2,
2,
2
] |
NCT02663622
|
1:24:chronic_disease
|
Uncontrolled infections
| 1
|
[
"Uncontrolled",
"infections"
] |
[
2,
2
] |
NCT02270450
|
20:47:chronic_disease,58:88:cancer,95:102:cancer,104:115:cancer,138:146:cancer,148:153:cancer,155:161:cancer,163:174:cancer,176:183:cancer,185:192:cancer,194:202:cancer,204:210:cancer,212:219:cancer,221:229:cancer,231:268:cancer,286:293:cancer
|
Patients must have malignant bowel obstruction due to an intra-abdominal primary cancer (i.e. stomach, small bowel [including duodenum], pancreas, colon, rectum, appendiceal, ovarian, uterine, cervical, kidney, bladder, prostate, gastrointestinal stromal tumor [GIST] [all sites], and sarcoma)
| 1
|
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NCT01954966
|
16:39:treatment,41:56:treatment,58:72:treatment,77:88:treatment,124:135:chronic_disease,150:159:treatment,164:180:chronic_disease,191:207:chronic_disease,209:235:chronic_disease,237:265:chronic_disease,267:297:chronic_disease,302:316:chronic_disease
|
Regular use of psychotropic medication (antidepressants, antipsychotics, or anxiolytics) and recent (within previous year) psychiatric diagnosis and treatment for Axis I disorders including major depression, bipolar affective disorder, generalized anxiety disorder, post-traumatic stress disorder and panic disorder
| 1
|
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NCT01996865
|
27:49:chronic_disease,55:78:chronic_disease,80:103:chronic_disease,105:139:chronic_disease
|
Known seropositive for or active viral infection with hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV)
| 1
|
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NCT03086057
|
1:4:chronic_disease
|
HIV Positive at baseline
| 1
|
[
"HIV",
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"at",
"baseline"
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[
2,
0,
0,
0
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NCT02004275
|
1:10:treatment,21:24:chronic_disease,36:52:treatment,,,
|
Treatment sensitive HIV and, if on anti-HIV therapy, HIV viral load < 50 copies/mm^3 within 28 days prior to registration
| 1
|
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NCT00887146
|
22:25:chronic_disease
|
patients known to be HIV positive, but without clinical evidence of an immunocompromised state
| 1
|
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"be",
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NCT02508467
|
65:68:treatment
|
For Part 3, the patient has not received prior treatment with a TKI
| 1
|
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NCT02516332
|
4:6:treatment,10:46:treatment,54:58:treatment,62:96:treatment,
|
An MI or coronary revascularization procedure (i.e., CABG or percutaneous coronary intervention) within the last 3 months
| 1
|
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NCT02004275
|
55:69:treatment
|
Patients randomized to Arm 1 may opt to switch to the 3-drug regimen following disease progression; these patients must be re-registered to the study and meet the eligibility criteria
| 1
|
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NCT02506192
|
25:30:chronic_disease
|
Has been diagnosed with Lupus
| 1
|
[
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] |
[
0,
0,
0,
0,
2
] |
NCT03182907
|
66:86:treatment
|
is currently participating in or scheduled to participate in any other clinical study with an investigational agent during the 12-week study period
| 1
|
[
"is",
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"any",
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NCT02830074
|
,,102:110:chronic_disease
|
the investigators will offer to re-contact patients 90 days after a health event or after 90 days of sobriety
| 1
|
[
"the",
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"will",
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"90",
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"90",
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NCT02100891
|
11:29:cancer,82:99:treatment,110:124:treatment
|
High Risk Neuroblastoma (NB): Must have progressed on or recurred after standard frontline therapy including autologous HCT, or be ineligible for autologous HCT
| 1
|
[
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"NB",
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NCT01990209
|
51:70:treatment
|
This group of patients may be pre-menopausal with ovarian suppression or post-menopausal
| 1
|
[
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NCT01714596
|
32:42:treatment
|
Patients who have high risk of amputation of the study limb (based on opinion of the initial managing physician)
| 1
|
[
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] |
NCT02589522
|
28:59:treatment,61:74:treatment,,116:120:treatment,,,298:318:treatment,332:354:treatment,,,404:416:treatment,420:431:treatment,477:486:treatment
|
Patients who have received systemic cytotoxic chemotherapy, immunotherapy for 3 weeks before initiation of planned WBRT or patients who have not recovered from serious (Common Terminology Criteria for Adverse Events [CTCAE] grade 3 or more) adverse events from the previously received agents; for oral targeted agents or any other investigational agents, at least 4 half-lives of the agent (6 weeks for nitrosoureas or mitomycin C) should have elapsed prior to starting study treatment
| 1
|
[
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NCT01045148
|
24:31:cancer,43:48:cancer,50:57:cancer,62:88:cancer,
|
Previous or concurrent cancers other than basal, in situ, or squamous cell skin cancers unless disease-free for ≥ 5 years
| 1
|
[
"Previous",
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"concurrent",
"cancers",
"other",
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",",
"in",
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"or",
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"cell",
"skin",
"cancers",
"unless",
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0,
0,
0
] |
NCT03101085
|
17:70:treatment
|
Use any type of systemic estrogen or testosterone replacement therapy
| 1
|
[
"Use",
"any",
"type",
"of",
"systemic",
"estrogen",
"or",
"testosterone",
"replacement",
"therapy"
] |
[
0,
0,
0,
0,
1,
1,
1,
1,
1,
1
] |
NCT00881660
|
16:28:chronic_disease
|
Preterm labor, preeclampsia
| 1
|
[
"Preterm",
"labor",
",",
"preeclampsia"
] |
[
0,
0,
0,
2
] |
NCT00929006
|
23:31:chronic_disease,,,,
|
Previous diagnosis of diabetes, fasting glucose > or = 126 mg/dl, or a hemoglobin A1c > or = 6.5%
| 1
|
[
"Previous",
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"of",
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"or",
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[
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0,
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0,
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0,
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] |
NCT01532687
|
7:17:cancer
|
Prior malignancy
| 1
|
[
"Prior",
"malignancy"
] |
[
0,
3
] |
NCT02665338
|
28:44:chronic_disease
|
Life time history of major Axis I disorders
| 1
|
[
"Life",
"time",
"history",
"of",
"major",
"Axis",
"I",
"disorders"
] |
[
0,
0,
0,
0,
0,
2,
2,
2
] |
NCT02696902
|
101:110:chronic_disease
|
expected to require prolonged intubation and mechanical ventilation, without any evidence of active pneumonia
| 1
|
[
"expected",
"to",
"require",
"prolonged",
"intubation",
"and",
"mechanical",
"ventilation",
",",
"without",
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT02561104
|
40:54:chronic_disease
|
Active, significant external ocular or eyelid disease
| 1
|
[
"Active",
",",
"significant",
"external",
"ocular",
"or",
"eyelid",
"disease"
] |
[
0,
0,
0,
0,
0,
0,
2,
2
] |
NCT02501954
|
23:60:treatment
|
Patients who have had pelvic or abdominal radiation therapy
| 1
|
[
"Patients",
"who",
"have",
"had",
"pelvic",
"or",
"abdominal",
"radiation",
"therapy"
] |
[
0,
0,
0,
0,
1,
1,
1,
1,
1
] |
NCT02000115
|
1:17:chronic_disease,30:40:cancer,,,63:69:chronic_disease,,,86:102:chronic_disease,,
|
Blood dyscrasias as defined: leukopenia (WBC<3000 mm3), acute anemia (Hb < 9 mg/dL), thrombocytopenia (platelet count <50,000 cells/mm³)
| 1
|
[
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",",
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"thrombocytopenia",
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"50,000",
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NCT02272556
|
19:26:treatment,
|
Current or recent steroid use in last 3 months
| 1
|
[
"Current",
"or",
"recent",
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0,
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0,
0,
0,
0
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NCT02323126
|
19:36:chronic_disease,40:57:chronic_disease,78:95:chronic_disease
|
positive test for hepatitis B virus or hepatitis C virus indicating acute or chronic infection
| 1
|
[
"positive",
"test",
"for",
"hepatitis",
"B",
"virus",
"or",
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"C",
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"chronic",
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0,
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0,
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2
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NCT01941316
|
37:54:treatment,
|
Patients may have received previous radiation therapy, but it must have been completed at least 21 days prior to enrollment and the patient should have recovered from all associated toxicities
| 1
|
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NCT03005782
|
1:23:treatment,,
|
Corticosteroid therapy (>10 mg prednisone/day or equivalent) within 1 week prior to the first dose of study drug
| 1
|
[
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NCT02648347
|
5:37:treatment,
|
Any erythropoietic stimulating agent within 8 weeks prior to randomization
| 1
|
[
"Any",
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"agent",
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"weeks",
"prior",
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NCT01526603
|
43:55:treatment,
|
Patients who are delayed in consolidation chemotherapy beyond 8 weeks
| 1
|
[
"Patients",
"who",
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"in",
"consolidation",
"chemotherapy",
"beyond",
"8",
"weeks"
] |
[
0,
0,
0,
0,
0,
0,
1,
0,
0,
0
] |
NCT03011307
|
18:36:chronic_disease
|
Suffering from a psychotic disorder
| 1
|
[
"Suffering",
"from",
"a",
"psychotic",
"disorder"
] |
[
0,
0,
0,
2,
2
] |
NCT01595529
|
56:64:allergy_name
|
A child with known anaphylactic allergies to the study products
| 1
|
[
"A",
"child",
"with",
"known",
"anaphylactic",
"allergies",
"to",
"the",
"study",
"products"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
4
] |
NCT00719888
|
,81:93:treatment
|
patients persistently aplastic for greater than one month since completing last chemotherapy are also eligible with PI approval
| 1
|
[
"patients",
"persistently",
"aplastic",
"for",
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"one",
"month",
"since",
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"are",
"also",
"eligible",
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NCT02287558
|
9:16:treatment,18:31:treatment,33:56:treatment,60:79:treatment
|
Chronic aspirin, NSAID therapy, anticoagulation therapy or antiplatelet agents
| 1
|
[
"Chronic",
"aspirin",
",",
"NSAID",
"therapy",
",",
"anticoagulation",
"therapy",
"or",
"antiplatelet",
"agents"
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0,
1,
0,
1,
1,
0,
1,
1,
0,
1,
1
] |
NCT02826577
|
1:19:chronic_disease
|
psychotic disorder
| 1
|
[
"psychotic",
"disorder"
] |
[
2,
2
] |
NCT02666638
|
15:30:chronic_disease,32:42:chronic_disease,44:56:cancer
|
no history of chronic illness, concussion, malignancies, etc
| 1
|
[
"no",
"history",
"of",
"chronic",
"illness",
",",
"concussion",
",",
"malignancies",
",",
"etc"
] |
[
0,
0,
0,
2,
2,
0,
2,
0,
3,
0,
0
] |
NCT02518594
|
32:45:cancer,110:120:treatment
|
Known, suspected or history of breast cancer because breast cancer is a contraindication to the active study medication
| 1
|
[
"Known",
",",
"suspected",
"or",
"history",
"of",
"breast",
"cancer",
"because",
"breast",
"cancer",
"is",
"a",
"contraindication",
"to",
"the",
"active",
"study",
"medication"
] |
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] |
NCT03043807
|
1:33:treatment,43:58:cancer,65:82:treatment,84:97:treatment
|
Prior local non-surgical therapy to treat prostate cancer (e.g. radiation therapy, brachytherapy)
| 1
|
[
"Prior",
"local",
"non-surgical",
"therapy",
"to",
"treat",
"prostate",
"cancer",
"(",
"e.g",
".",
"radiation",
"therapy",
",",
"brachytherapy",
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1,
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3,
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0,
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1,
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0,
1,
0
] |
NCT01951885
|
35:69:chronic_disease
|
Patients who are seropositive for human immunodeficiency virus (HIV)
| 1
|
[
"Patients",
"who",
"are",
"seropositive",
"for",
"human",
"immunodeficiency",
"virus",
"(",
"HIV",
")"
] |
[
0,
0,
0,
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT02837510
|
1:20:treatment
|
Anti-anxiety agents
| 1
|
[
"Anti-anxiety",
"agents"
] |
[
1,
1
] |
NCT03139227
|
,,47:59:treatment
|
Must be > 1 year from pregnancy, lactation or chemotherapy
| 1
|
[
"Must",
"be",
">",
"1",
"year",
"from",
"pregnancy",
",",
"lactation",
"or",
"chemotherapy"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT01379573
|
22:37:treatment,88:96:treatment,242:245:treatment,,278:281:chronic_disease
|
Mother is taking any glucocorticoids. Although unlikely to be preventative, the use of steroids may confound the interpretation of results. The final point of intense discussion centered around whether another exclusion should be the use of HCQ in the first pregnancy in which CHB occurred. While one could argue that in these mothers HCQ was not effective and perhaps will not be again, this assumption remains speculative and thus prior absence of efficacy of HCQ will not constitute an exclusion criteria
| 1
|
[
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"to",
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"preventative",
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"final",
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"an",
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NCT01624090
|
61:81:treatment
|
Normal ionized calcium, magnesium and phosphorus (can be on oral supplementation)
| 1
|
[
"Normal",
"ionized",
"calcium",
",",
"magnesium",
"and",
"phosphorus",
"(",
"can",
"be",
"on",
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"supplementation",
")"
] |
[
0,
0,
0,
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0,
0,
0,
0,
0,
0,
0,
1,
1,
0
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NCT02108860
|
16:19:treatment,
|
Treatment with CYC within 3 months prior to screening
| 1
|
[
"Treatment",
"with",
"CYC",
"within",
"3",
"months",
"prior",
"to",
"screening"
] |
[
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
NCT01952730
|
,37:49:treatment,51:63:treatment,65:78:treatment,89:111:treatment
|
At least 4 weeks since last dose of chemotherapy, radiotherapy, immunotherapy, systemic glucocorticoid therapy or operation in order to receive vaccine
| 1
|
[
"At",
"least",
"4",
"weeks",
"since",
"last",
"dose",
"of",
"chemotherapy",
",",
"radiotherapy",
",",
"immunotherapy",
",",
"systemic",
"glucocorticoid",
"therapy",
"or",
"operation",
"in",
"order",
"to",
"receive",
"vaccine"
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[
0,
0,
0,
0,
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0,
0,
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0,
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0,
1,
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0,
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1,
0,
0,
0,
0,
0,
0,
0
] |
NCT01967238
|
36:42:chronic_disease,44:48:chronic_disease,52:69:chronic_disease,103:124:chronic_disease
|
Documented previous infection with dengue, zika or chikungunya virus or no history of dengue, zika or chikungunya infection
| 1
|
[
"Documented",
"previous",
"infection",
"with",
"dengue",
",",
"zika",
"or",
"chikungunya",
"virus",
"or",
"no",
"history",
"of",
"dengue",
",",
"zika",
"or",
"chikungunya",
"infection"
] |
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0,
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0,
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] |
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