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1.5k
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list | ner_tags
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|---|---|---|---|---|---|
NCT02495545
|
18:21:chronic_disease
|
Prior history of SCI
| 1
|
[
"Prior",
"history",
"of",
"SCI"
] |
[
0,
0,
0,
2
] |
NCT01953900
|
53:65:treatment
|
Recovered from the acute toxic effects of all prior chemotherapy
| 1
|
[
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[
0,
0,
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0,
0,
0,
0,
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1
] |
NCT02966665
|
43:47:chronic_disease,49:52:chronic_disease,54:56:chronic_disease,61:73:chronic_disease
|
Subject has physical ailments (other than COPD, PAH, HF, or hypertension) that would prevent them from study participation in the judgment of the investigator
| 1
|
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NCT02484404
|
59:71:chronic_disease
|
Patients with a history of previous clinical diagnosis of tuberculosis are not eligible
| 1
|
[
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NCT01876511
|
28:72:treatment
|
Requires any other form of systemic or localized antineoplastic therapy while on study
| 1
|
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NCT01730794
|
37:49:treatment
|
Immunosuppressed patients receiving chemotherapy
| 1
|
[
"Immunosuppressed",
"patients",
"receiving",
"chemotherapy"
] |
[
0,
0,
0,
1
] |
NCT02498951
|
,53:65:treatment
|
Effective contraception is required while receiving obinutuzumab
| 1
|
[
"Effective",
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[
0,
0,
0,
0,
0,
0,
1
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NCT02245997
|
15:19:cancer,,
|
Patients with INSS stage 2a or 2b
| 1
|
[
"Patients",
"with",
"INSS",
"stage",
"2a",
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"2b"
] |
[
0,
0,
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0,
0,
0,
0
] |
NCT02074436
|
1:26:chronic_disease
|
Grade 2 renal dysfunction
| 1
|
[
"Grade",
"2",
"renal",
"dysfunction"
] |
[
2,
2,
2,
2
] |
NCT01666665
|
1:14:chronic_disease
|
renal failure
| 1
|
[
"renal",
"failure"
] |
[
2,
2
] |
NCT02758847
|
1:13:treatment
|
chemotherapy
| 1
|
[
"chemotherapy"
] |
[
1
] |
NCT02315196
|
,81:93:treatment
|
imaging must have been performed no greater than 30 days prior to initiation of chemotherapy
| 1
|
[
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NCT02770326
|
22:32:allergy_name
|
Contraindications to anesthesia for procedure
| 1
|
[
"Contraindications",
"to",
"anesthesia",
"for",
"procedure"
] |
[
0,
0,
4,
0,
0
] |
NCT01850758
|
35:49:chronic_disease,92:112:chronic_disease,114:142:chronic_disease,144:163:chronic_disease,165:176:chronic_disease,178:190:chronic_disease,192:207:chronic_disease
|
Inflammatory or auto-immune based joint diseases or other lower extremity pathology (e.g., rheumatoid arthritis, systemic lupus erythematosus, psoriatic arthritis, polymyalgia, polymyositis, gout pseudogout)
| 1
|
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"rheumatoid",
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NCT03179397
|
1:10:chronic_disease
|
Amblyopia
| 1
|
[
"Amblyopia"
] |
[
2
] |
NCT00739362
|
1:14:chronic_disease,,
|
Renal disease (serum creatinine concentrations greater than or equal to 1.5 mg/dl and/or overt proteinuria)
| 1
|
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NCT02004275
|
16:48:treatment
|
progression on lenalidomide maintenance therapy after initial induction +/- consolidation
| 1
|
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"progression",
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NCT02981082
|
1:45:chronic_disease
|
Moderate to severe interstitial lung disease
| 1
|
[
"Moderate",
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"severe",
"interstitial",
"lung",
"disease"
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[
2,
2,
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2,
2,
2
] |
NCT03082612
|
42:54:treatment
|
Have completed surgery with no plans for chemotherapy
| 1
|
[
"Have",
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"with",
"no",
"plans",
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] |
[
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02437773
|
16:26:treatment
|
Not taking any medication, prescription or non-prescription, with psychotropic effects
| 1
|
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0,
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0,
0,
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0
] |
NCT02826382
|
12:31:chronic_disease
|
history of hyperparathyroidism
| 1
|
[
"history",
"of",
"hyperparathyroidism"
] |
[
0,
0,
2
] |
NCT02835729
|
7:10:chronic_disease
|
Known HIV-infected patients
| 1
|
[
"Known",
"HIV-infected",
"patients"
] |
[
0,
2,
0
] |
NCT03127358
|
37:45:allergy_name,47:58:allergy_name,63:72:allergy_name
|
Known hypersensitivity (allergy) to elbasvir, grazoprevir, or ribavirin
| 1
|
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NCT02501473
|
29:40:chronic_disease,55:63:treatment,94:119:chronic_disease
|
History of (non-infectious) pneumonitis that required steroids or has current pneumonitis or interstitial lung disease
| 1
|
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NCT02530034
|
65:87:chronic_disease,78:87:chronic_disease,,,,225:244:chronic_disease,308:321:chronic_disease,342:363:chronic_disease,,402:425:chronic_disease,450:461:chronic_disease,480:490:treatment,508:532:chronic_disease,,,
|
Uncontrolled intercurrent illness including, but not limited to uncontrolled infection (patients must have no temperature >= 38.3 degree Celsius [C] due to infection for at least 48 hrs to consider an infection controlled), psychiatric illness that would limit compliance with study requirements, or active heart disease including confirmed myocardial infarction within previous 3 months, symptomatic coronary artery disease, clinically significant arrhythmias not controlled by medication, or uncontrolled congestive heart failure New York (NY) Heart Association class III or IV
| 1
|
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NCT01953575
|
33:48:treatment
|
undergoing clinically indicated upper endoscopy
| 1
|
[
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"indicated",
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] |
[
0,
0,
0,
1,
1
] |
NCT02269124
|
32:55:chronic_disease
|
with mild to moderately severe unilateral hearing loss
| 1
|
[
"with",
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"severe",
"unilateral",
"hearing",
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[
0,
0,
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0,
2,
2,
2
] |
NCT02547662
|
13:37:cancer,39:77:cancer,53:62:cancer
|
EXCEPTIONS: Non-melanoma skin cancer, ductal breast carcinoma in situ (DCIS) or carcinoma-in-situ of the cervix
| 1
|
[
"EXCEPTIONS",
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NCT02365766
|
23:37:treatment,69:77:treatment,81:116:treatment,
|
Subjects on full dose anticoagulants must be on a stable regimen of warfarin or low molecular weight heparin (LMWH) for at least two weeks
| 1
|
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NCT02310464
|
21:36:treatment
|
Uses of inhaled and topical steroids are allowed
| 1
|
[
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0,
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0,
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NCT00720785
|
52:63:cancer
|
Disease not evaluable radiographically (applies to solid tumor patients only)
| 1
|
[
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NCT02844465
|
,34:64:chronic_disease
|
MRI has evidence consistent with mesial temporal lobe sclerosis
| 1
|
[
"MRI",
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[
0,
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2,
2
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NCT03177265
|
20:28:chronic_disease
|
ICD 9 diagnosis of dementia (excluded during data abstraction process)
| 1
|
[
"ICD",
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NCT01269034
|
1:9:chronic_disease
|
diabetes
| 1
|
[
"diabetes"
] |
[
2
] |
NCT03001830
|
31:44:chronic_disease,,
|
confirmed diagnosis of severe Haemophilia A defined as baseline plasma FVIII levels of <1% of normal as assessed by a validated one-stage clotting assay or a chromogenic assay, resulting from intron 22 inversions, intron 1 inversions, splice-site mutations, small deletions/insertions and missense mutations
| 1
|
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NCT02209636
|
1:15:chronic_disease
|
CKD stage IIIb
| 1
|
[
"CKD",
"stage",
"IIIb"
] |
[
2,
2,
2
] |
NCT03070535
|
1:6:chronic_disease,11:25:chronic_disease,27:47:chronic_disease
|
Liver and kidney disease: Active liver disease will be excluded
| 1
|
[
"Liver",
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"liver",
"disease",
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[
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0,
2,
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2,
0,
0,
0
] |
NCT02551679
|
13:42:chronic_disease
|
Uncorrected aorto-iliac occlusive disease
| 1
|
[
"Uncorrected",
"aorto-iliac",
"occlusive",
"disease"
] |
[
0,
2,
2,
2
] |
NCT02305537
|
107:116:treatment
|
those who report that they are unwilling to refrain from self-injurious behaviors during the waitlist and treatment periods
| 1
|
[
"those",
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"that",
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"are",
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"to",
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"during",
"the",
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"treatment",
"periods"
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0,
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NCT03040778
|
15:38:chronic_disease
|
Patients with ischemic heart diseases
| 1
|
[
"Patients",
"with",
"ischemic",
"heart",
"diseases"
] |
[
0,
0,
2,
2,
2
] |
NCT02496585
|
41:51:chronic_disease,,,,,
|
Inherited predisposition to bleeding or thrombosis, INR >2, PT and PTT >1.5x ULN
| 1
|
[
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NCT01595061
|
34:44:chronic_disease,53:62:chronic_disease,64:89:chronic_disease,100:125:chronic_disease,136:163:treatment
|
Patients with evidence of active septicemia, severe infection, gastrointestinal bleeding or severe gastrointestinal symptoms requiring medical or surgical therapy
| 1
|
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] |
NCT01239160
|
14:38:chronic_disease
|
Diagnosis of congestive heart failure (uncontrolled)
| 1
|
[
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NCT02033616
|
18:33:chronic_disease,50:72:chronic_disease,87:111:treatment
|
Known underlying cardiac disease associated with myocardial dysfunction that requires active medical treatment
| 1
|
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NCT01989585
|
1:17:treatment,19:33:treatment,39:52:treatment
|
Prior navitoclax, BRAF inhibitor, and MEK inhibitor is prohibited; (exceptions for Phase I are described above)
| 1
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NCT02573597
|
1:11:chronic_disease
|
ASA I & II
| 1
|
[
"ASA",
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[
2,
2,
2,
2
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NCT03153982
|
1:14:treatment,19:39:cancer,110:126:treatment,,202:211:treatment,304:324:treatment
|
Prior therapy for head and neck cancer is allowed, and the number of treatments is not limited. However, any systemic therapy should have been completed at least 30 days prior to study enrollment. Any radiation to the head and neck should have been completed at least 30 days prior to study enrollment. Palliative radiation outside of the head and neck does not require a washout
| 1
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NCT01859819
|
1:53:cancer
|
B-Cell Anaplastic Large cell Ki 1 positive lymphomas
| 1
|
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3,
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NCT01445821
|
10:13:treatment,69:86:treatment,259:279:chronic_disease,283:313:treatment
|
Abnormal EKG [non-specific ST-segment and T-wave (ST-T) (pattern in electrocardiogram) wave abnormalities, low QRS (a pattern seen in an electrocardiogram that indicates the pulses in a heart beat and their duration) voltage, or ventricular hypertrophy], or pericardial effusion or pericardial enhancement on MRI
| 1
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NCT00788164
|
13:23:chronic_disease
|
Symptomatic arrhythmia not controlled by medication
| 1
|
[
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[
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NCT01894061
|
,56:66:treatment,68:94:chronic_disease,103:118:chronic_disease,120:155:treatment,157:187:chronic_disease,189:219:chronic_disease,221:252:chronic_disease,254:277:chronic_disease
|
Any of the following within 6 months prior to starting study drug: myocardial infarction (MI), severe/unstable angina, Coronary Artery Bypass Graft (CABG), Congestive Heart Failure (CHF), Cerebrovascular Accident (CVA), Transient Ischemic Attack (TIA), Pulmonary Embolism (PE)
| 1
|
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NCT02089607
|
1:27:chronic_disease
|
Uncorrectable coagulopathy
| 1
|
[
"Uncorrectable",
"coagulopathy"
] |
[
2,
2
] |
NCT02312596
|
7:20:chronic_disease,,
|
Known renal failure as determined by a Creatinine > 2.5 mg/dl
| 1
|
[
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NCT02584647
|
,,,,,,150:159:treatment
|
Creatinine ≤ 1.5 x ULN or calculated creatinine clearance (CrCl) > 60 mL/min using the Cockcroft-Gault formula less than eight days pior to start of treatment
| 1
|
[
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NCT02728050
|
12:23:treatment
|
The use of hydroxyurea prior to study registration
| 1
|
[
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NCT02169739
|
23:39:chronic_disease,46:69:treatment,79:101:chronic_disease
|
Known history of limb vascular disease, limb vascular bypass surgery, or limb deep venous thrombosis
| 1
|
[
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NCT00887146
|
21:28:treatment,50:65:treatment,67:79:treatment,72:79:treatment
|
patients with prior surgery cannot have received prior radiation, chemotherapy or targeted therapy
| 1
|
[
"patients",
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1
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NCT02471430
|
30:44:chronic_disease
|
History or other evidence of severe illness or other conditions
| 1
|
[
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"severe",
"illness",
"or",
"other",
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[
0,
0,
0,
0,
0,
2,
2,
0,
0,
0
] |
NCT01037790
|
1:25:cancer,,,,155:166:treatment,171:188:treatment,
|
Metastatic breast cancer (7 triple negative, 23 ER+ after the first 15 patients are enrolled on the non-CCND1cohort; in addition 10 HER2+ for combination trastuzumab and PD0332991 therapy) up to 55 total enrollment slots B
| 1
|
[
"Metastatic",
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NCT02111850
|
,,122:131:treatment
|
Women of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects of the treatment on the fetus
| 1
|
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NCT02350764
|
15:38:chronic_disease,40:54:chronic_disease,70:89:treatment,110:116:chronic_disease,117:122:chronic_disease,155:190:treatment,192:206:chronic_disease,216:224:chronic_disease,226:235:chronic_disease,240:248:chronic_disease,264:282:treatment
|
Subjects with type I diabetes melitis, hypothyroidism only requiring hormone replacement, resolved childhood asthma/atopy, patients with asthma requiring intermittent bronchodilator therapy, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger
| 1
|
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NCT02257424
|
15:31:cancer,45:56:treatment,60:67:treatment,,250:261:treatment
|
patients with brain metastases treated with gamma knife or surgery are allowed to participate after 3 weeks have elapsed since their procedure . Demonstration of brain stability by an imaging study after the procedure is required for gamma knife or CNS surgery patients
| 1
|
[
"patients",
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NCT02414269
|
25:49:treatment,92:109:treatment,113:136:treatment
|
A requirement for daily systemic corticosteroids for any reason or a requirement for other immunosuppressive or immunomodulatory agents
| 1
|
[
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NCT01659203
|
1:34:chronic_disease
|
Uncontrolled intercurrent illness
| 1
|
[
"Uncontrolled",
"intercurrent",
"illness"
] |
[
2,
2,
2
] |
NCT02595866
|
77:86:chronic_disease
|
Mild autoimmunity not impacting the function of major organs (e.g., limited psoriasis)
| 1
|
[
"Mild",
"autoimmunity",
"not",
"impacting",
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"of",
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"limited",
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0
] |
NCT02158793
|
1:23:chronic_disease
|
Serious co-morbidities
| 1
|
[
"Serious",
"co-morbidities"
] |
[
2,
2
] |
NCT02481245
|
,46:61:treatment
|
Subjects having failed two or more trials of somatic therapy
| 1
|
[
"Subjects",
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"two",
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"more",
"trials",
"of",
"somatic",
"therapy"
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[
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02437812
|
27:37:cancer,
|
Subjects with concomitant malignancy or a previous malignancy within the past three years
| 1
|
[
"Subjects",
"with",
"concomitant",
"malignancy",
"or",
"a",
"previous",
"malignancy",
"within",
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"three",
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[
0,
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NCT02603757
|
29:41:treatment
|
Patients who do not undergo chemotherapy
| 1
|
[
"Patients",
"who",
"do",
"not",
"undergo",
"chemotherapy"
] |
[
0,
0,
0,
0,
0,
1
] |
NCT02089607
|
51:72:chronic_disease
|
Absence of a non-aneurysmal aortic segment in the distal thoracic aorta above the diaphragmatic hiatus
| 1
|
[
"Absence",
"of",
"a",
"non-aneurysmal",
"aortic",
"segment",
"in",
"the",
"distal",
"thoracic",
"aorta",
"above",
"the",
"diaphragmatic",
"hiatus"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
0
] |
NCT02203903
|
15:38:chronic_disease
|
Patients with uncontrolled infections
| 1
|
[
"Patients",
"with",
"uncontrolled",
"infections"
] |
[
0,
0,
2,
2
] |
NCT02531932
|
24:51:treatment,59:71:treatment,73:85:treatment,87:96:treatment,101:121:treatment
|
Co-administration with strong inhibitors of CYP3A4 (e.g., ketoconazole, itraconazole, ritonavir) or P-glycoprotein (PgP)
| 1
|
[
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"itraconazole",
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0
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NCT01672138
|
22:39:chronic_disease,48:63:chronic_disease,65:76:chronic_disease,78:96:chronic_disease
|
Reversible causes of atrial arrhythmia such as hyperthyroidism, sarcoidosis, pulmonary embolism etc
| 1
|
[
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"arrhythmia",
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",",
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",",
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[
0,
0,
0,
2,
2,
0,
0,
2,
0,
2,
0,
2,
2,
0
] |
NCT01817751
|
37:43:cancer,,,80:104:treatment,108:140:treatment
|
Pathologically confirmed high-grade glioma (WHO grade 3 or 4), with documented computed tomography (CT) or magnetic resonance imaging (MRI) progression or recurrence
| 1
|
[
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"confirmed",
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"WHO",
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"CT",
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"MRI",
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1,
1,
1,
1,
0,
0,
0,
0,
0
] |
NCT01966367
|
10:17:chronic_disease
|
Adequate cardiac function per protocol
| 1
|
[
"Adequate",
"cardiac",
"function",
"per",
"protocol"
] |
[
0,
2,
0,
0,
0
] |
NCT02446093
|
13:16:chronic_disease
|
Known to be HIV+
| 1
|
[
"Known",
"to",
"be",
"HIV+"
] |
[
0,
0,
0,
2
] |
NCT02991651
|
45:52:allergy_name,56:65:allergy_name,93:101:allergy_name,105:125:allergy_name
|
History of allergic reactions attributed to IRX4204 or erlotinib or to compounds of similar chemical or biologic composition
| 1
|
[
"History",
"of",
"allergic",
"reactions",
"attributed",
"to",
"IRX4204",
"or",
"erlotinib",
"or",
"to",
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"composition"
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0,
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0,
0,
0,
4,
0,
4,
4
] |
NCT02845596
|
16:50:chronic_disease
|
Infection with human immunodeficiency virus (HIV)
| 1
|
[
"Infection",
"with",
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"immunodeficiency",
"virus",
"(",
"HIV",
")"
] |
[
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT02637349
|
30:39:chronic_disease,41:49:chronic_disease,51:65:chronic_disease
|
Altered mental status (e.g., psychosis, delirium, disorientation)
| 1
|
[
"Altered",
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"e.g.",
",",
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[
0,
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0,
0,
0,
0,
2,
0,
2,
0,
2,
0
] |
NCT02931110
|
19:22:cancer,26:29:cancer,,85:112:treatment,,
|
For subjects with ALL or AML, presence of >5% blasts in the bone marrow (based on a bone marrow aspirate/biopsy sample with ≥200 nucleated cells and the presence of bone marrow spicules)
| 1
|
[
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NCT02078102
|
13:21:cancer
|
Transformed lymphoma
| 1
|
[
"Transformed",
"lymphoma"
] |
[
0,
3
] |
NCT02927392
|
,26:44:treatment
|
Women who have undergone surgical menopause
| 1
|
[
"Women",
"who",
"have",
"undergone",
"surgical",
"menopause"
] |
[
0,
0,
0,
0,
1,
1
] |
NCT02547818
|
20:51:treatment,59:68:treatment,103:114:treatment,
|
subjects receiving acetylcholinesterase inhibitors and/or memantine should be on stable dose of those medications for at least 12 weeks prior to study start with every effort to maintain stable dose for the duration of the study
| 1
|
[
"subjects",
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0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02912572
|
8:26:chronic_disease
|
Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent
| 1
|
[
"Active",
"autoimmune",
"disease",
"that",
"might",
"deteriorate",
"when",
"receiving",
"an",
"immunostimulatory",
"agent"
] |
[
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01905709
|
,,,,86:96:treatment,128:138:treatment,146:155:treatment,157:169:treatment,171:182:treatment
|
At least three episodes of mild-to-moderate CDI and failure of a 6-8 week taper with vancomycin with or without an alternative antibiotic (e.g., rifaximin, nitazoxanide, fidaxomicin)
| 1
|
[
"At",
"least",
"three",
"episodes",
"of",
"mild-to-moderate",
"CDI",
"and",
"failure",
"of",
"a",
"6-8",
"week",
"taper",
"with",
"vancomycin",
"with",
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"without",
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"(",
"e.g.",
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"rifaximin",
",",
"nitazoxanide",
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0,
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1,
0,
0,
0,
1,
0,
1,
0,
1,
0
] |
NCT02387216
|
,13:52:treatment
|
Received >2 prior systemic anti-cancer drug regimen for locally advanced disease
| 1
|
[
"Received",
">",
"2",
"prior",
"systemic",
"anti-cancer",
"drug",
"regimen",
"for",
"locally",
"advanced",
"disease"
] |
[
0,
0,
0,
1,
1,
1,
1,
1,
0,
0,
0,
0
] |
NCT01925573
|
40:52:cancer,62:87:cancer,108:119:cancer,121:144:cancer
|
Patients with recurrent or progressive glioblastoma or other grade IV malignant glioma (i.e. glioblastoma, gliosarcoma, giant cell glioblastoma, etc.)
| 1
|
[
"Patients",
"with",
"recurrent",
"or",
"progressive",
"glioblastoma",
"or",
"other",
"grade",
"IV",
"malignant",
"glioma",
"(",
"i.e",
".",
"glioblastoma",
",",
"gliosarcoma",
",",
"giant",
"cell",
"glioblastoma",
",",
"etc",
".",
")"
] |
[
0,
0,
0,
0,
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0,
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3,
0,
3,
3,
3,
0,
0,
0,
0
] |
NCT03109210
|
1:17:chronic_disease,25:31:cancer,37:70:chronic_disease,78:86:chronic_disease
|
terminal illness (e.g., cancer), or neurological degenerative disease (e.g., dementia)
| 1
|
[
"terminal",
"illness",
"(",
"e.g.",
",",
"cancer",
")",
",",
"or",
"neurological",
"degenerative",
"disease",
"(",
"e.g.",
",",
"dementia",
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] |
[
2,
2,
0,
0,
0,
3,
0,
0,
0,
2,
2,
2,
0,
0,
0,
2,
0
] |
NCT02131805
|
55:64:treatment,66:81:treatment,85:99:treatment
|
Receipt of drug that will affect biologic response to radiation (radiosensitizer or radioprotector)
| 1
|
[
"Receipt",
"of",
"drug",
"that",
"will",
"affect",
"biologic",
"response",
"to",
"radiation",
"(",
"radiosensitizer",
"or",
"radioprotector",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1,
0
] |
NCT02694029
|
12:28:chronic_disease
|
ongoing or active infection
| 1
|
[
"ongoing",
"or",
"active",
"infection"
] |
[
0,
0,
2,
2
] |
NCT01822522
|
1:42:treatment
|
Prior treatment with cabozantinib (XL184)
| 1
|
[
"Prior",
"treatment",
"with",
"cabozantinib",
"(",
"XL184",
")"
] |
[
1,
1,
1,
1,
1,
0,
0
] |
NCT02759575
|
18:42:chronic_disease
|
Known history of active tuberculosis (TB)
| 1
|
[
"Known",
"history",
"of",
"active",
"tuberculosis",
"(",
"TB",
")"
] |
[
0,
0,
0,
2,
2,
2,
0,
0
] |
NCT02914171
|
,67:89:treatment
|
Individuals with the following conditions within 60 days prior to Ebstein repair surgery
| 1
|
[
"Individuals",
"with",
"the",
"following",
"conditions",
"within",
"60",
"days",
"prior",
"to",
"Ebstein",
"repair",
"surgery"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02132598
|
,99:108:treatment
|
Patients must have normal organ and marrow function as defined below: (within 4 days of beginning treatment unless noted otherwise)
| 1
|
[
"Patients",
"must",
"have",
"normal",
"organ",
"and",
"marrow",
"function",
"as",
"defined",
"below",
":",
"(",
"within",
"4",
"days",
"of",
"beginning",
"treatment",
"unless",
"noted",
"otherwise",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0
] |
NCT02425566
|
1:23:chronic_disease
|
cardiovascular disease
| 1
|
[
"cardiovascular",
"disease"
] |
[
2,
2
] |
NCT02373644
|
21:43:chronic_disease
|
Patient must report sacroiliac dysfunction
| 1
|
[
"Patient",
"must",
"report",
"sacroiliac",
"dysfunction"
] |
[
0,
0,
0,
2,
2
] |
NCT02236013
|
46:58:treatment,
|
documented surgically sterile or status post hysterectomy (at least 1 month prior to Screening)
| 1
|
[
"documented",
"surgically",
"sterile",
"or",
"status",
"post",
"hysterectomy",
"(",
"at",
"least",
"1",
"month",
"prior",
"to",
"Screening",
")"
] |
[
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02427997
|
11:19:chronic_disease,,
|
free from dementia as determined using the Mini Mental State Exam (MMSE>=24)
| 1
|
[
"free",
"from",
"dementia",
"as",
"determined",
"using",
"the",
"Mini",
"Mental",
"State",
"Exam",
"(",
"MMSE",
">",
"=24",
")"
] |
[
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02482376
|
34:43:treatment
|
Subjects unable to receive study treatment planning secondary to body habitus or inability to lie flat on the stomach at length
| 1
|
[
"Subjects",
"unable",
"to",
"receive",
"study",
"treatment",
"planning",
"secondary",
"to",
"body",
"habitus",
"or",
"inability",
"to",
"lie",
"flat",
"on",
"the",
"stomach",
"at",
"length"
] |
[
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02092324
|
28:48:chronic_disease
|
subjects with a history of Hepatitis B and/or C are allowed on trial if the virus is undetected at the time of enrollment
| 1
|
[
"subjects",
"with",
"a",
"history",
"of",
"Hepatitis",
"B",
"and/or",
"C",
"are",
"allowed",
"on",
"trial",
"if",
"the",
"virus",
"is",
"undetected",
"at",
"the",
"time",
"of",
"enrollment"
] |
[
0,
0,
0,
0,
0,
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2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
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