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1.5k
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list | ner_tags
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|---|---|---|---|---|---|
NCT02687464
|
39:47:cancer
|
presentation with an appendix mass or phlegmon (on physical examination and/or imaging)
| 1
|
[
"presentation",
"with",
"an",
"appendix",
"mass",
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"phlegmon",
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0,
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NCT03002389
|
12:43:chronic_disease
|
History of alpha 1 anti-trypsin deficiency
| 1
|
[
"History",
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"anti-trypsin",
"deficiency"
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[
0,
0,
2,
2,
2,
2
] |
NCT02015390
|
35:50:cancer
|
Disseminated and/or nonresectable malignant tumor involving bone
| 1
|
[
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"tumor",
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[
0,
0,
0,
3,
3,
0,
0
] |
NCT02131597
|
,,,,,157:170:treatment
|
Women who are able to become pregnant and men who can father a child must use birth control while on study and for at least 8 weeks after your last dose of study drug(s)
| 1
|
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NCT02180412
|
,149:158:chronic_disease
|
Acute symptoms (7 days duration or less to time of enrollment) such as abdominal, back and/or limb pain, diagnosed by the investigator as caused by porphyria after initial evaluation has excluded other causes
| 1
|
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NCT03090607
|
,,41:52:treatment
|
GERD-HRQL score ≥15 after discontinuing PPI therapy
| 1
|
[
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NCT02200445
|
,,,104:113:treatment,
|
Men and women of reproductive potential must agree to use an acceptable method of birth control during treatment and for six months after completion of treatment
| 1
|
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NCT02236013
|
76:85:treatment
|
Subject agrees not to participate in another interventional study while on treatment
| 1
|
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0,
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0,
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NCT01174121
|
42:72:treatment
|
Grade 3 or 4 major organ irAEs following treatment with anti-PD-1/PD-L1
| 1
|
[
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NCT02099591
|
49:61:treatment
|
Patients currently receiving the first cycle of chemotherapy
| 1
|
[
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0,
0,
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0,
0,
0,
0,
1
] |
NCT02003222
|
18:30:treatment
|
RANDOMIZATION TO BLINATUMOMAB OR NO BLINATUMOMAB-STEP 3
| 1
|
[
"RANDOMIZATION",
"TO",
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"OR",
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"BLINATUMOMAB-STEP",
"3"
] |
[
0,
0,
1,
0,
0,
0,
0
] |
NCT01532687
|
1:23:chronic_disease
|
Malabsorption syndrome
| 1
|
[
"Malabsorption",
"syndrome"
] |
[
2,
2
] |
NCT02091999
|
1:13:treatment
|
chemotherapy
| 1
|
[
"chemotherapy"
] |
[
1
] |
NCT02315612
|
47:51:treatment,86:93:chronic_disease,150:177:treatment
|
(For children who are unable to cooperate for PFTs, the criterion is: No evidence of dyspnea at rest, no exercise intolerance and no requirement for supplemental oxygen therapy. )
| 1
|
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NCT02503722
|
15:24:treatment,28:34:treatment,64:89:treatment,
|
substrates of CYP 3A4/5 or CYP1A2 that are sensitive or have a narrow therapeutic window at least three weeks prior to study registration
| 1
|
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NCT02478684
|
11:31:chronic_disease
|
Any major congenital anomalies
| 1
|
[
"Any",
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"congenital",
"anomalies"
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[
0,
0,
2,
2
] |
NCT02565901
|
1:20:chronic_disease,31:49:chronic_disease,68:75:treatment
|
Atrial fibrillation, or other cardiac arrhythmia requiring medical therapy
| 1
|
[
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0,
0,
2,
2,
0,
0,
1
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NCT01676259
|
10:20:chronic_disease
|
unstable arrhythmia
| 1
|
[
"unstable",
"arrhythmia"
] |
[
0,
2
] |
NCT01648023
|
15:37:chronic_disease,,
|
Patients with liver-dominant disease defined as ≥80% tumor burden confined to the liver
| 1
|
[
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] |
NCT02407028
|
25:58:treatment,,112:122:treatment,123:134:treatment,138:162:treatment
|
Ability to initiate the first hyperbaric oxygen treatment within 14 hours of admission in patients requiring a craniotomy/craniectomy or major surgical procedure
| 1
|
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NCT01543490
|
40:49:treatment
|
provide documentation for having had a vasectomy (with documented infertility)
| 1
|
[
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NCT02592707
|
20:29:treatment,33:43:treatment,72:79:cancer,84:92:cancer,124:150:treatment
|
In countries where sunitinib or everolimus are marketed, patients with GEP NET and lung NET will be progressive under this prior anti-tumor treatment for the respective indication
| 1
|
[
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NCT02531880
|
19:22:chronic_disease
|
Positive test for HIV
| 1
|
[
"Positive",
"test",
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"HIV"
] |
[
0,
0,
0,
2
] |
NCT02037048
|
,40:52:treatment
|
for 90 days following the last dose of chemotherapy
| 1
|
[
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[
0,
0,
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NCT02953509
|
1:26:treatment
|
Prior treatment with CD47
| 1
|
[
"Prior",
"treatment",
"with",
"CD47"
] |
[
1,
1,
1,
1
] |
NCT02061761
|
1:19:chronic_disease
|
Autoimmune disease
| 1
|
[
"Autoimmune",
"disease"
] |
[
2,
2
] |
NCT02347995
|
1:9:chronic_disease
|
dementia by clinical evaluation
| 1
|
[
"dementia",
"by",
"clinical",
"evaluation"
] |
[
2,
0,
0,
0
] |
NCT02264678
|
37:48:allergy_name
|
Contra-indicated for treatment with carboplatin
| 1
|
[
"Contra-indicated",
"for",
"treatment",
"with",
"carboplatin"
] |
[
0,
0,
0,
0,
4
] |
NCT02639065
|
49:61:chronic_disease
|
Known history of previous clinical diagnosis of tuberculosis
| 1
|
[
"Known",
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"previous",
"clinical",
"diagnosis",
"of",
"tuberculosis"
] |
[
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT02167958
|
1:13:treatment
|
Chemotherapy-sensitive (complete or partial response
| 1
|
[
"Chemotherapy-sensitive",
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"partial",
"response"
] |
[
1,
0,
0,
0,
0,
0
] |
NCT02311361
|
,,,,,,255:264:treatment
|
Enrolled patients must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, the duration of study participation and 180 days (female patients) or 90 days (male patients) after the end of the treatment
| 1
|
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NCT02240498
|
10:46:chronic_disease
|
Severely compromised cardiopulmonary function
| 1
|
[
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NCT02498613
|
73:83:cancer,112:146:cancer,152:187:cancer,,,,284:310:treatment,350:391:treatment,417:449:cancer,458:487:cancer
|
Patients must have histologically confirmed, metastatic or unresectable malignancy of the following types: (a) non-small cell lung cancer (NSCLC), (b) triple-negative breast cancer (TNBC; defined by estrogen receptor [ER] < 1%, progesterone receptor [PR] < 1% and HER2 1+ or less by immunohistochemistry [IHC]; if HER-2 expression is 2+, a negative fluorescence in situ hybridization [FISH] testing is required) (c) pancreatic adenocarcinoma (PDAC), or (d) small cell lung cancer (SCLC)
| 1
|
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NCT02525029
|
16:45:cancer
|
Diagnosis of a hormone responsive malignancy
| 1
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NCT02302976
|
35:49:chronic_disease,54:74:chronic_disease,79:106:chronic_disease,135:157:chronic_disease,160:166:chronic_disease,180:219:chronic_disease,221:238:chronic_disease,251:279:treatment,281:301:chronic_disease,310:336:chronic_disease,338:344:chronic_disease,353:361:chronic_disease
|
a history of significant medical (cardiovascular) or neurological illness, ie prior myocardial infarction, current active symptoms of cardiovascular disease / angina, evidence of cocaine-related cardiovascular symptoms, prior arrhythmias or need for cardiovascular resuscitation, neurovascular events such as transient ischemic attacks, stroke, and/or seizures Parameters re: elevations in vital signs are now explicitly specified under Safety features built into our one-day self-administration paradigm)
| 1
|
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NCT02369653
|
1:14:treatment,26:73:treatment,78:100:treatment,105:120:treatment,
|
Major surgery [excluding Central Venous Access Device (CVAD) replacement and bone marrow aspiration and non-open biopsy] within the last 7 days prior to enrollment that may be associated with a risk of bleeding
| 1
|
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NCT02667418
|
36:65:treatment,
|
Anticipation of need for long term systemic antibiotic treatment (beyond 7 days)
| 1
|
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NCT01333046
|
,54:64:treatment,68:81:treatment,86:102:treatment
|
Patients greater than or equal to 18 years old after autologous or syngeneic SCT (as adjuvant therapy)
| 1
|
[
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NCT03042689
|
14:35:chronic_disease,78:94:chronic_disease,108:132:chronic_disease,134:159:chronic_disease,161:185:chronic_disease,200:218:chronic_disease,223:260:chronic_disease
|
Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, uncontrolled cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
| 1
|
[
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NCT02098252
|
53:72:treatment
|
Hemorrhagic presentation with mass effect requiring surgical management
| 1
|
[
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0,
0,
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1,
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NCT00065676
|
1:25:chronic_disease
|
congestive heart failure
| 1
|
[
"congestive",
"heart",
"failure"
] |
[
2,
2,
2
] |
NCT02819635
|
1:19:treatment
|
immunosuppressants
| 1
|
[
"immunosuppressants"
] |
[
1
] |
NCT00432094
|
23:46:chronic_disease
|
Patients with serious uncontrolled infections
| 1
|
[
"Patients",
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"uncontrolled",
"infections"
] |
[
0,
0,
0,
2,
2
] |
NCT02012296
|
21:33:treatment,
|
Record of subject's enzalutamide start date and baseline PSA (within 28 days of starting) before starting enzalutamide available
| 1
|
[
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NCT02520791
|
24:57:cancer,61:102:cancer,,138:153:treatment
|
Confirmed diagnosis of peripheral T-cell lymphoma (PTCL) or angioimmunoblastic T-cell lymphoma (AITL) that is refractory to at least one line of therapy
| 1
|
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NCT02365766
|
1:26:cancer
|
Clinical stage cT2-4aN0M0
| 1
|
[
"Clinical",
"stage",
"cT2-4aN0M0"
] |
[
3,
3,
3
] |
NCT02982759
|
63:71:chronic_disease
|
Exclusion criteria include children with clinically-diagnosed dementia
| 1
|
[
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[
0,
0,
0,
0,
0,
0,
2
] |
NCT02842658
|
49:62:cancer
|
Subjects will have been recently diagnosed with breast cancer
| 1
|
[
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[
0,
0,
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0,
0,
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3,
3
] |
NCT02505035
|
1:45:chronic_disease,
|
Chronic obstructive pulmonary disease (COPD) with home oxygen dependence or 2 or more hospitalizations in the past 12 months
| 1
|
[
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NCT02191098
|
39:50:chronic_disease
|
History or evidence of uncontrollable CNS disease
| 1
|
[
"History",
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"CNS",
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] |
[
0,
0,
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0,
0,
2,
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NCT01140087
|
1:4:chronic_disease
|
HIV positive
| 1
|
[
"HIV",
"positive"
] |
[
2,
0
] |
NCT02389465
|
1:4:allergy_name,30:55:allergy_name,57:66:allergy_name
|
MRI contraindications (e.g., foreign metallic implants, pacemaker)
| 1
|
[
"MRI",
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"(",
"e.g.",
",",
"foreign",
"metallic",
"implants",
",",
"pacemaker",
")"
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[
4,
0,
0,
0,
0,
4,
4,
4,
0,
4,
0
] |
NCT02165007
|
7:28:treatment
|
First allogeneic transplant
| 1
|
[
"First",
"allogeneic",
"transplant"
] |
[
0,
1,
1
] |
NCT02232516
|
1:18:chronic_disease,62:80:cancer,112:116:cancer
|
topical treatment may have been given for prior existence of cutaneous lymphoma that has since become systemic PTCL
| 1
|
[
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] |
NCT03067571
|
61:79:chronic_disease
|
has any concurrent medical condition or disease (eg, active systemic infection, laboratory abnormalities) that is likely to interfere with study procedures or results, or that in the opinion of the investigator would constitute a hazard for participating in this study
| 1
|
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NCT03059888
|
24:36:chronic_disease
|
Subject is at risk for tuberculosis
| 1
|
[
"Subject",
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"tuberculosis"
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[
0,
0,
0,
0,
0,
2
] |
NCT02524379
|
22:30:treatment,
|
Known treatment with Bosentan within past 7 days
| 1
|
[
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"7",
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] |
[
0,
0,
0,
1,
0,
0,
0,
0
] |
NCT03179605
|
15:24:chronic_disease,,
|
Subjects with psoriasis involving ≥10% Body Surface Area (BSA), not including the face, scalp, groin, axillae and other intertriginous areas at the Baseline Visit
| 1
|
[
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NCT01730118
|
27:36:treatment,40:60:treatment,91:104:cancer
|
Stable, concurrent use of tamoxifen or aromatase inhibitors for hormone receptor positive breast cancer are allowed
| 1
|
[
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NCT01983475
|
,16:28:chronic_disease
|
Men with known hypogonadism prior to SCI
| 1
|
[
"Men",
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"SCI"
] |
[
0,
0,
0,
2,
0,
0,
0
] |
NCT02429830
|
13:22:chronic_disease,,
|
Symptoms of dysphagia more than once per week within the last 3 months
| 1
|
[
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0,
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0
] |
NCT02323191
|
,,60:69:treatment,,
|
Negative serum pregnancy test within 7 days prior to study treatment in premenopausal women and women less than or equal to (<=) 12 months post-menopause
| 1
|
[
"Negative",
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NCT03021902
|
1:54:chronic_disease
|
Pre-existing cognitive impairment or language barrier that prohibits outcomes assessment
| 1
|
[
"Pre-existing",
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"language",
"barrier",
"that",
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"outcomes",
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[
2,
2,
2,
2,
2,
2,
0,
0,
0,
0
] |
NCT02057133
|
13:35:treatment,73:105:treatment,,124:156:treatment,158:169:treatment,171:180:treatment,186:204:cancer,234:257:treatment
|
For Part D (LY2835219 + exemestane): The participant must have received prior systemic endocrine therapy with at least one nonsteroidal aromatase inhibitor (anastrozole, letrozole) for metastatic disease and may be receiving ongoing therapy with exemestane
| 1
|
[
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NCT01996449
|
21:34:allergy_name
|
Hypersensitivity to nitroprusside
| 1
|
[
"Hypersensitivity",
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] |
[
0,
0,
4
] |
NCT02473250
|
1:15:treatment,17:26:treatment,28:44:treatment,46:74:treatment,78:86:treatment
|
Metal implants, pacemaker, metal prostheses, metal orthodontic appliances or shrapnel in the body
| 1
|
[
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",",
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0,
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] |
NCT03008408
|
88:100:treatment,,
|
Patients in whom ovaries are present and were not previously menopausal at the time of hysterectomy, should have a serum estradiol <10 pm/mL to confirm ovarian senescence
| 1
|
[
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NCT02495168
|
21:30:treatment
|
on the first day of treatment (prior to randomization at Visit 2)
| 1
|
[
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NCT02250664
|
36:51:chronic_disease,101:110:treatment,114:127:treatment,
|
Be in good physical health without serious illness or change in health or medication (not including methadone or buprenorphine dose) in the past three months as determined by the license medical professional at each site
| 1
|
[
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NCT02562716
|
,,,151:163:treatment
|
women/men of reproductive potential must have agreed to use an effective contraceptive method for up to 3 months after the final administered dose of chemotherapy
| 1
|
[
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NCT02152995
|
11:20:treatment,,
|
All prior treatment-related toxicities must be Common Terminology Criteria for Adverse Events version 4.0 (CTCAE v 4.0) grade =< 1
| 1
|
[
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"Adverse",
"Events",
"version",
"4.0",
"(",
"CTCAE",
"v",
"4.0",
")",
"grade",
"=",
"<",
"1"
] |
[
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01940757
|
12:34:chronic_disease
|
History of iron deficiency anemia
| 1
|
[
"History",
"of",
"iron",
"deficiency",
"anemia"
] |
[
0,
0,
2,
2,
2
] |
NCT02437370
|
40:53:allergy_name
|
Has known hypersensitivity to MK-3475 (pembrolizumab) or any of its incipients
| 1
|
[
"Has",
"known",
"hypersensitivity",
"to",
"MK-3475",
"(",
"pembrolizumab",
")",
"or",
"any",
"of",
"its",
"incipients"
] |
[
0,
0,
0,
0,
0,
0,
4,
0,
0,
0,
0,
0,
0
] |
NCT02193373
|
19:26:chronic_disease
|
Current or recent illness
| 1
|
[
"Current",
"or",
"recent",
"illness"
] |
[
0,
0,
0,
2
] |
NCT01464034
|
,52:64:treatment,
|
Male pts cannot donate semen or sperm while taking pomalidomide and for 28 days after completing the study
| 1
|
[
"Male",
"pts",
"can",
"not",
"donate",
"semen",
"or",
"sperm",
"while",
"taking",
"pomalidomide",
"and",
"for",
"28",
"days",
"after",
"completing",
"the",
"study"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02784535
|
21:32:allergy_name
|
Hypersensitivity to atomoxetine
| 1
|
[
"Hypersensitivity",
"to",
"atomoxetine"
] |
[
0,
0,
4
] |
NCT02991677
|
,15:35:treatment
|
History of >1 chemotherapy regimen
| 1
|
[
"History",
"of",
">",
"1",
"chemotherapy",
"regimen"
] |
[
0,
0,
0,
0,
1,
1
] |
NCT02064036
|
10:28:treatment,30:52:treatment,57:78:treatment
|
Previous pelvic irradiation, prostate brachytherapy, or bilateral orchiectomy
| 1
|
[
"Previous",
"pelvic",
"irradiation",
",",
"prostate",
"brachytherapy",
",",
"or",
"bilateral",
"orchiectomy"
] |
[
0,
1,
1,
0,
1,
1,
0,
0,
1,
1
] |
NCT02128906
|
48:64:chronic_disease,66:87:chronic_disease,89:114:chronic_disease
|
No uncontrolled intercurrent illness including active infection, uncontrolled diabetes, uncontrolled hypertension
| 1
|
[
"No",
"uncontrolled",
"intercurrent",
"illness",
"including",
"active",
"infection",
",",
"uncontrolled",
"diabetes",
",",
"uncontrolled",
"hypertension"
] |
[
0,
2,
2,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT02102113
|
29:38:chronic_disease
|
Having a family member with psychosis
| 1
|
[
"Having",
"a",
"family",
"member",
"with",
"psychosis"
] |
[
0,
0,
0,
0,
0,
2
] |
NCT02332369
|
14:30:chronic_disease
|
Preoperative ocular infection
| 1
|
[
"Preoperative",
"ocular",
"infection"
] |
[
0,
2,
2
] |
NCT02582827
|
34:42:chronic_disease,51:69:treatment,71:78:treatment,83:95:treatment,
|
All adverse events (AEs) (except alopecia) of any prior chemotherapy, surgery, or radiotherapy must have resolved to Grade ≤ 1
| 1
|
[
"All",
"adverse",
"events",
"(",
"AEs",
")",
"(",
"except",
"alopecia",
")",
"of",
"any",
"prior",
"chemotherapy",
",",
"surgery",
",",
"or",
"radiotherapy",
"must",
"have",
"resolved",
"to",
"Grade",
"≤",
"1"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
1,
1,
0,
1,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02760498
|
28:50:treatment
|
Patients with a history of solid organ transplant
| 1
|
[
"Patients",
"with",
"a",
"history",
"of",
"solid",
"organ",
"transplant"
] |
[
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02519322
|
,,,,184:207:treatment
|
WOCBP must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]) within 24 hours prior to the start of investigational product
| 1
|
[
"WOCBP",
"must",
"have",
"a",
"negative",
"serum",
"or",
"urine",
"pregnancy",
"test",
"(",
"minimum",
"sensitivity",
"25",
"IU/L",
"or",
"equivalent",
"units",
"of",
"human",
"chorionic",
"gonadotropin",
"[",
"HCG",
"]",
")",
"within",
"24",
"hours",
"prior",
"to",
"the",
"start",
"of",
"investigational",
"product"
] |
[
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
] |
NCT02710396
|
,25:35:chronic_disease
|
Subjects with ≤ Grade 2 neuropathy are an exception to this criterion and may qualify for the study
| 1
|
[
"Subjects",
"with",
"≤",
"Grade",
"2",
"neuropathy",
"are",
"an",
"exception",
"to",
"this",
"criterion",
"and",
"may",
"qualify",
"for",
"the",
"study"
] |
[
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02924194
|
8:32:treatment
|
Use of cholinesterase inhibitor
| 1
|
[
"Use",
"of",
"cholinesterase",
"inhibitor"
] |
[
0,
0,
1,
1
] |
NCT02564744
|
79:97:treatment
|
For Part 2 and Part 3 of the study, participants that are eligible to undergo first time HD-ASCT
| 1
|
[
"For",
"Part",
"2",
"and",
"Part",
"3",
"of",
"the",
"study",
",",
"participants",
"that",
"are",
"eligible",
"to",
"undergo",
"first",
"time",
"HD-ASCT"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT01415752
|
,,,45:58:chronic_disease,60:79:chronic_disease,101:124:chronic_disease,129:149:treatment,168:176:chronic_disease
|
Patients must not have NYHA Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia
| 1
|
[
"Patients",
"must",
"not",
"have",
"NYHA",
"Class",
"III",
"or",
"IV",
"heart",
"failure",
",",
"uncontrolled",
"angina",
",",
"severe",
"uncontrolled",
"ventricular",
"arrhythmias",
",",
"or",
"electrocardiographic",
"evidence",
"of",
"acute",
"ischemia"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
2,
2,
0,
0,
0,
2,
2,
0,
0,
1,
0,
0,
0,
2
] |
NCT00902720
|
21:49:treatment
|
patients undergoing elective removal of an ovary for fertility preservation only
| 1
|
[
"patients",
"undergoing",
"elective",
"removal",
"of",
"an",
"ovary",
"for",
"fertility",
"preservation",
"only"
] |
[
0,
0,
1,
1,
1,
1,
1,
0,
0,
0,
0
] |
NCT02397889
|
,,100:120:treatment
|
Women of childbearing potential must have a negative pregnancy test at screening and prior to each intravenous infusion
| 1
|
[
"Women",
"of",
"childbearing",
"potential",
"must",
"have",
"a",
"negative",
"pregnancy",
"test",
"at",
"screening",
"and",
"prior",
"to",
"each",
"intravenous",
"infusion"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT03104725
|
10:43:treatment
|
Taking a monoamine oxidase (MAO) inhibitor
| 1
|
[
"Taking",
"a",
"monoamine",
"oxidase",
"(",
"MAO",
")",
"inhibitor"
] |
[
0,
0,
1,
1,
1,
1,
0,
0
] |
NCT03092635
|
1:19:treatment,
|
Prior chemotherapy is allowed, but last dose must have been at least 2 months prior to enrollment
| 1
|
[
"Prior",
"chemotherapy",
"is",
"allowed",
",",
"but",
"last",
"dose",
"must",
"have",
"been",
"at",
"least",
"2",
"months",
"prior",
"to",
"enrollment"
] |
[
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02740543
|
1:19:chronic_disease,28:60:chronic_disease,64:89:chronic_disease
|
Pulmonary diseases such as Chronic Pulmonary Disease (COPD) or Interstitial Lung Disease
| 1
|
[
"Pulmonary",
"diseases",
"such",
"as",
"Chronic",
"Pulmonary",
"Disease",
"(",
"COPD",
")",
"or",
"Interstitial",
"Lung",
"Disease"
] |
[
2,
2,
0,
0,
2,
2,
2,
2,
0,
0,
0,
2,
2,
2
] |
NCT02169739
|
1:33:treatment,,112:120:chronic_disease
|
Diffusion-weighted imaging (DWI) lesion < 2.0cm in size at largest dimension and corresponding to the clinical syndrome
| 1
|
[
"Diffusion-weighted",
"imaging",
"(",
"DWI",
")",
"lesion",
"<",
"2.0cm",
"in",
"size",
"at",
"largest",
"dimension",
"and",
"corresponding",
"to",
"the",
"clinical",
"syndrome"
] |
[
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT00492778
|
23:35:treatment
|
Patients who received chemotherapy directed at the present recurrence
| 1
|
[
"Patients",
"who",
"received",
"chemotherapy",
"directed",
"at",
"the",
"present",
"recurrence"
] |
[
0,
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT02669173
|
23:37:treatment
|
Patients on full-dose anticoagulants
| 1
|
[
"Patients",
"on",
"full-dose",
"anticoagulants"
] |
[
0,
0,
0,
1
] |
NCT02272998
|
28:55:treatment
|
Patients who have received prior FGFR targeted therapy
| 1
|
[
"Patients",
"who",
"have",
"received",
"prior",
"FGFR",
"targeted",
"therapy"
] |
[
0,
0,
0,
0,
1,
1,
1,
1
] |
NCT00338377
|
15:18:treatment,31:34:cancer,64:86:cancer
|
Patients with MRI evidence of LMD, with or without evidence of malignant cells in CSF (positive cytology)
| 1
|
[
"Patients",
"with",
"MRI",
"evidence",
"of",
"LMD",
",",
"with",
"or",
"without",
"evidence",
"of",
"malignant",
"cells",
"in",
"CSF",
"(",
"positive",
"cytology",
")"
] |
[
0,
0,
1,
0,
0,
3,
0,
0,
0,
0,
0,
0,
3,
3,
3,
3,
0,
0,
0,
0
] |
NCT03158974
|
1:24:treatment,
|
Topical corticosteroids if greater than 2 gm/day
| 1
|
[
"Topical",
"corticosteroids",
"if",
"greater",
"than",
"2",
"gm/day"
] |
[
1,
1,
0,
0,
0,
0,
0
] |
NCT02573883
|
8:11:chronic_disease
|
Active UTI
| 1
|
[
"Active",
"UTI"
] |
[
0,
2
] |
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