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NCT02191098
|
1:37:chronic_disease,39:63:chronic_disease,68:89:chronic_disease,
|
Symptomatic congestive heart failure, unstable angina pectoris, or Myocardial infarction within 6 months prior to screening
| 3
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NCT02392572
|
63:78:cancer,82:95:cancer,118:127:treatment
|
For Arms A, B, C, D patients must have relapsed or refractory acute leukemias or high-risk MDS for which no standard therapies are anticipated to result in a durable remission
| 3
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NCT01880567
|
21:24:cancer,49:71:chronic_disease,108:119:chronic_disease,121:145:chronic_disease,149:170:chronic_disease,,,,250:265:chronic_disease,
|
Relapsed/refractory MCL: Clinically significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure or myocardial infarction within 6 months at the time of consent or any class 3 (moderate) or 4 (severe) cardiac disease defined by the New York Heart Association classification
| 3
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NCT02452268
|
13:28:treatment,37:43:cancer,50:65:treatment,58:65:treatment,70:85:cancer
|
Subjects on bisphosphonates for any cancer or on hormone therapy for prostate cancer may continue this therapy
| 3
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NCT02349867
|
11:24:chronic_disease
|
Suspected malabsorption or obstruction
| 3
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NCT02570984
|
,24:43:treatment,
|
More than one night of albuterol treatment (for symptoms) in the past two weeks
| 3
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NCT01994382
|
9:18:treatment,31:56:treatment,58:77:treatment,79:101:treatment
|
Chronic treatment with strong CYP3A4 inhibitor/ inducer, acid reducing agent, Proton pump inhibitors
| 3
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NCT02774421
|
14:25:chronic_disease
|
uncontrolled arrhythmias
| 3
|
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NCT02058095
|
29:32:chronic_disease,,
|
A total of 39 patients with PDD as defined by an ejection fraction of greater than 50%
| 3
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NCT02304458
|
,26:40:chronic_disease
|
Patients with >= grade 2 hypothyroidism due to history of autoimmunity
| 3
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NCT02807272
|
1:22:chronic_disease
|
myocardial infarction within the prior year
| 3
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NCT01445821
|
4:18:treatment,,,,100:122:chronic_disease,126:169:chronic_disease
|
On echocardiogram tricuspid annular peak systolic excursion (TAPSE) ≤ 1.8 cm or, grade II or worse Right Ventricular (RV) or Left Ventricular (LV) diastolic dysfunction
| 3
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NCT02772562
|
23:27:allergy_name,29:41:allergy_name,43:69:allergy_name
|
History of allergy to eggs, egg products, aminoglycoside antibiotics
| 3
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NCT02389309
|
32:64:allergy_name
|
History of hypersensitivity to any component of the formulation
| 3
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NCT02132598
|
,,,,218:228:treatment
|
For this reason women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for 4 months after the last dose of study drug, even if oral contraceptives are used
| 3
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NCT01795573
|
73:82:treatment,217:249:treatment,267:294:treatment,385:405:treatment
|
HL: No clinical evidence of disease or disease-related symptoms; A post-treatment residual mass of any size is permitted as long as it is PET negative; Spleen and liver must be non-palpable and without nodules; If a pre-treatment bone marrow biopsy was positive, an adequate bone marrow biopsy from the same site must be cleared of infiltrate; if this is indeterminate by morphology, immunohistochemistry should be negative
| 3
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NCT02522715
|
12:19:chronic_disease,110:122:chronic_disease,124:130:chronic_disease,,153:173:cancer,175:191:cancer,193:207:chronic_disease
|
history of seizure or any condition that may predispose to seizure including, but not limited to, underlying brain injury, stroke in the past 6 months, primary brain tumors, brain metastases, prior seizures
| 3
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NCT02473536
|
23:35:treatment,,
|
Subjects who have had radiotherapy to a target within 3 cm of the IVC tumor thrombus
| 3
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NCT02930018
|
8:16:allergy_name,57:75:allergy_name,87:112:treatment,235:262:chronic_disease,300:310:treatment
|
Severe contrast allergy or absolute contraindication to iodinated contrast preventing endovascular intervention, including any contraindications listed in the prescribing information approved by local authorities (e.g., patients with decompensated heart failure as a contraindication for the use of VISIPAQUE™ 270 in Germany
| 3
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NCT02035085
|
1:17:treatment
|
Metallic implant
| 3
|
[
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[
1,
1
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NCT02412540
|
1:16:chronic_disease
|
hemochromatosis
| 3
|
[
"hemochromatosis"
] |
[
2
] |
NCT00391170
|
32:45:allergy_name
|
Documented hypersensitivity to dexamethasone
| 3
|
[
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[
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NCT02012296
|
1:20:chronic_disease,24:48:treatment,49:81:treatment
|
Progressive disease on computed tomography (CT)/magnetic resonance imaging (MRI) according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria
| 3
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NCT02191488
|
12:25:chronic_disease,
|
History of liver disease within the last 12 months
| 3
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NCT03023696
|
56:75:chronic_disease,85:98:chronic_disease,117:149:treatment,,,238:259:treatment,264:284:treatment
|
Cleveland Clinic patients who have been diagnosed with cervical myelopathy, without radiculopathy, and will undergo posterior cervical decompression involving the C4-C5 interspace between 2016 and 2018. This includes patients undergoing cervical laminoplasty and cervical laminectomy and fusion
| 3
|
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NCT02412540
|
23:45:treatment,63:89:treatment,,128:140:treatment
|
Current enrollment in another clinical trial or receipt of an investigational study drug within 6 months prior to the baseline liver biopsy
| 3
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NCT02387905
|
56:59:treatment
|
Patients unable to undergo magnetic resonance imaging (MRI) of the spine
| 3
|
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NCT02687906
|
55:66:treatment
|
subjects receiving peri-operative prophylactic use of antibiotics
| 3
|
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NCT02981082
|
,13:31:chronic_disease
|
ACR defined systemic sclerosis
| 3
|
[
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[
0,
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2
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NCT02301663
|
1:9:chronic_disease
|
Diabetes
| 3
|
[
"Diabetes"
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[
2
] |
NCT02553642
|
28:52:treatment,
|
Patients may have received prior focal radiotherapy for palliation of an isolated site of disease, which must be completed at least 14 days prior to day 1 of the study
| 3
|
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NCT01220583
|
1:16:chronic_disease,24:48:chronic_disease,59:74:treatment,
|
Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months
| 3
|
[
"Unstable",
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"and/or",
"congestive",
"heart",
"failure",
"requiring",
"hospitalization",
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NCT02033486
|
16:39:treatment
|
presenting for breast cancer treatment
| 3
|
[
"presenting",
"for",
"breast",
"cancer",
"treatment"
] |
[
0,
0,
1,
1,
1
] |
NCT02746458
|
1:11:treatment
|
skin graft
| 3
|
[
"skin",
"graft"
] |
[
1,
1
] |
NCT02923011
|
56:71:cancer
|
Patients must have medically uncontrolled pain from an osteoid osteoma, as defined by pain, which, in the view of the referring orthopedic oncologist significantly interferes with that patient's activities of daily living
| 3
|
[
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NCT02101944
|
,,30:41:treatment
|
Platelet count >= 75,000 and transfusion independent
| 3
|
[
"Platelet",
"count",
">",
"=",
"75,000",
"and",
"transfusion",
"independent"
] |
[
0,
0,
0,
0,
0,
0,
1,
0
] |
NCT01893307
|
1:20:chronic_disease
|
hematologic disease
| 3
|
[
"hematologic",
"disease"
] |
[
2,
2
] |
NCT02915744
|
24:42:treatment
|
Concomitant use of any anticancer therapy or use of any investigational agent(s)
| 3
|
[
"Concomitant",
"use",
"of",
"any",
"anticancer",
"therapy",
"or",
"use",
"of",
"any",
"investigational",
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"(",
"s",
")"
] |
[
0,
0,
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1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00969332
|
8:29:chronic_disease
|
recent myocardial infarction
| 3
|
[
"recent",
"myocardial",
"infarction"
] |
[
0,
2,
2
] |
NCT02234557
|
44:48:chronic_disease,76:95:chronic_disease,100:113:chronic_disease
|
Children must meet diagnostic criteria for ADHD on the Kiddie Schedule for Affective Disorders and Schizophrenia
| 3
|
[
"Children",
"must",
"meet",
"diagnostic",
"criteria",
"for",
"ADHD",
"on",
"the",
"Kiddie",
"Schedule",
"for",
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"Disorders",
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"Schizophrenia"
] |
[
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
2,
2,
0,
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] |
NCT03109041
|
17:35:treatment
|
Patient has had prior chemotherapy
| 3
|
[
"Patient",
"has",
"had",
"prior",
"chemotherapy"
] |
[
0,
0,
0,
1,
1
] |
NCT02643381
|
55:64:treatment
|
Any patient who has been previously randomized in the EvK Trial
| 3
|
[
"Any",
"patient",
"who",
"has",
"been",
"previously",
"randomized",
"in",
"the",
"EvK",
"Trial"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02188121
|
1:37:treatment
|
Concomitant psychotropic medications will be allowed
| 3
|
[
"Concomitant",
"psychotropic",
"medications",
"will",
"be",
"allowed"
] |
[
1,
1,
1,
0,
0,
0
] |
NCT02665338
|
1:38:chronic_disease
|
Post-traumatic Stress disorder (PTSD)
| 3
|
[
"Post-traumatic",
"Stress",
"disorder",
"(",
"PTSD",
")"
] |
[
2,
2,
2,
2,
0,
0
] |
NCT02323880
|
1:24:treatment
|
Concomitant medications
| 3
|
[
"Concomitant",
"medications"
] |
[
1,
1
] |
NCT01101451
|
29:36:chronic_disease
|
Patients with postoperative fistula
| 3
|
[
"Patients",
"with",
"postoperative",
"fistula"
] |
[
0,
0,
0,
2
] |
NCT03059888
|
82:87:chronic_disease,89:96:chronic_disease,98:109:chronic_disease,111:127:chronic_disease,129:138:chronic_disease,140:147:chronic_disease,149:159:chronic_disease,163:179:chronic_disease
|
Subject has the presence at screening of any severe, progressive or uncontrolled renal, hepatic, hematologic, gastrointestinal, pulmonary, cardiac, neurologic or cerebral disease, whether or not related to MG that, in the opinion of the Investigator, might place the subject at unacceptable risk for participation in the study
| 3
|
[
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"the",
"presence",
"at",
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"of",
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"progressive",
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"hepatic",
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"hematologic",
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"gastrointestinal",
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"pulmonary",
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NCT03185208
|
14:39:chronic_disease
|
Diagnosis of Mild Cognitive Impairment
| 3
|
[
"Diagnosis",
"of",
"Mild",
"Cognitive",
"Impairment"
] |
[
0,
0,
2,
2,
2
] |
NCT00065676
|
1:20:chronic_disease
|
renal insufficiency
| 3
|
[
"renal",
"insufficiency"
] |
[
2,
2
] |
NCT02498301
|
23:34:treatment,
|
Subject's duration of prophylaxis will be least 2 weeks
| 3
|
[
"Subject",
"'s",
"duration",
"of",
"prophylaxis",
"will",
"be",
"least",
"2",
"weeks"
] |
[
0,
0,
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT02436070
|
1:27:chronic_disease
|
Inflammatory bowel disease
| 3
|
[
"Inflammatory",
"bowel",
"disease"
] |
[
2,
2,
2
] |
NCT02563678
|
,32:48:treatment,52:75:treatment,79:97:treatment,115:127:treatment
|
Use in the past 30 days of any over-the-counter or prescription medication or dietary supplement beyond a general multivitamin
| 3
|
[
"Use",
"in",
"the",
"past",
"30",
"days",
"of",
"any",
"over-the-counter",
"or",
"prescription",
"medication",
"or",
"dietary",
"supplement",
"beyond",
"a",
"general",
"multivitamin"
] |
[
0,
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0,
0,
0,
0,
0,
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0,
1,
1,
0,
1,
1,
0,
0,
0,
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] |
NCT01868386
|
12:25:treatment
|
have had a prostatectomy
| 3
|
[
"have",
"had",
"a",
"prostatectomy"
] |
[
0,
0,
0,
1
] |
NCT02259504
|
21:66:treatment
|
Intended or planned aneurysm treatment by parent vessel occlusion
| 3
|
[
"Intended",
"or",
"planned",
"aneurysm",
"treatment",
"by",
"parent",
"vessel",
"occlusion"
] |
[
0,
0,
0,
1,
1,
1,
1,
1,
1
] |
NCT01585402
|
22:32:treatment
|
Known sensitivity to etidronate
| 3
|
[
"Known",
"sensitivity",
"to",
"etidronate"
] |
[
0,
0,
0,
1
] |
NCT02816736
|
1:24:chronic_disease,,54:80:treatment,107:126:chronic_disease
|
Acute coronary syndrome within 4 weeks as defined by electrocardiographic (ECG) changes and biomarkers of myocardial necrosis (e.g. troponin) in an appropriate clinical setting (chest discomfort or anginal equivalent)
| 3
|
[
"Acute",
"coronary",
"syndrome",
"within",
"4",
"weeks",
"as",
"defined",
"by",
"electrocardiographic",
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"ECG",
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"changes",
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"biomarkers",
"of",
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"necrosis",
"(",
"e.g",
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"troponin",
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"in",
"an",
"appropriate",
"clinical",
"setting",
"(",
"chest",
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"or",
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"equivalent",
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0,
0,
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0,
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NCT02995733
|
12:15:treatment
|
Prescribed ICS as daily maintenance therapy
| 3
|
[
"Prescribed",
"ICS",
"as",
"daily",
"maintenance",
"therapy"
] |
[
0,
1,
0,
0,
0,
0
] |
NCT00358657
|
15:31:chronic_disease,79:91:treatment,107:125:treatment,
|
Patients with fungal pneumonia with radiological progression after receipt of amphotericin formulation or mold-active azoles for greater than 1 month
| 3
|
[
"Patients",
"with",
"fungal",
"pneumonia",
"with",
"radiological",
"progression",
"after",
"receipt",
"of",
"amphotericin",
"formulation",
"or",
"mold-active",
"azoles",
"for",
"greater",
"than",
"1",
"month"
] |
[
0,
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2,
0,
0,
0,
0,
0,
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0,
0,
1,
1,
0,
0,
0,
0,
0
] |
NCT02624258
|
1:3:chronic_disease
|
HL with biopsy-proven relapse
| 3
|
[
"HL",
"with",
"biopsy-proven",
"relapse"
] |
[
2,
0,
0,
0
] |
NCT03150511
|
9:27:chronic_disease
|
Certain pituitary problems
| 3
|
[
"Certain",
"pituitary",
"problems"
] |
[
0,
2,
2
] |
NCT02504489
|
19:26:treatment
|
Modification of a regimen to manage toxicity with a different drug does not constitute a new regimen
| 3
|
[
"Modification",
"of",
"a",
"regimen",
"to",
"manage",
"toxicity",
"with",
"a",
"different",
"drug",
"does",
"not",
"constitute",
"a",
"new",
"regimen"
] |
[
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02394028
|
5:37:treatment,
|
Any prior treatment with ustekinumab within 14 weeks prior to randomization
| 3
|
[
"Any",
"prior",
"treatment",
"with",
"ustekinumab",
"within",
"14",
"weeks",
"prior",
"to",
"randomization"
] |
[
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT02778867
|
6:10:treatment
|
on a 6FED
| 3
|
[
"on",
"a",
"6FED"
] |
[
0,
0,
1
] |
NCT02053792
|
38:51:treatment,
|
Life-threatening bleeding episode or major surgery during the 3 months prior to substudy entry
| 3
|
[
"Life-threatening",
"bleeding",
"episode",
"or",
"major",
"surgery",
"during",
"the",
"3",
"months",
"prior",
"to",
"substudy",
"entry"
] |
[
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02471833
|
16:51:treatment
|
Current use of renin-angiotensin acting medication
| 3
|
[
"Current",
"use",
"of",
"renin-angiotensin",
"acting",
"medication"
] |
[
0,
0,
0,
1,
1,
1
] |
NCT01697293
|
5:10:cancer,84:99:treatment,101:148:treatment
|
the tumor must be human epidermal growth factor receptor 2 (Her2)/neu negative (by DAKO HercepTest, fluorescence based in situ hybridization [FISH], or other approved assay)
| 3
|
[
"the",
"tumor",
"must",
"be",
"human",
"epidermal",
"growth",
"factor",
"receptor",
"2",
"(",
"Her2",
")",
"/neu",
"negative",
"(",
"by",
"DAKO",
"HercepTest",
",",
"fluorescence",
"based",
"in",
"situ",
"hybridization",
"[",
"FISH",
"]",
",",
"or",
"other",
"approved",
"assay",
")"
] |
[
0,
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0,
1,
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01686373
|
23:30:chronic_disease
|
Patients must have an aphasia diagnosis as confirmed by the Western Aphasia Battery-Revised
| 3
|
[
"Patients",
"must",
"have",
"an",
"aphasia",
"diagnosis",
"as",
"confirmed",
"by",
"the",
"Western",
"Aphasia",
"Battery-Revised"
] |
[
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01568918
|
1:40:treatment
|
Cervical Anterior Discectomy and Fusion
| 3
|
[
"Cervical",
"Anterior",
"Discectomy",
"and",
"Fusion"
] |
[
1,
1,
1,
1,
1
] |
NCT01625923
|
5:18:chronic_disease
|
Has gastroparesis at screening (gastric half-time of emptying > upper limit of normal as determined by wireless motility capsule)
| 3
|
[
"Has",
"gastroparesis",
"at",
"screening",
"(",
"gastric",
"half-time",
"of",
"emptying",
">",
"upper",
"limit",
"of",
"normal",
"as",
"determined",
"by",
"wireless",
"motility",
"capsule",
")"
] |
[
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02209545
|
1:21:treatment
|
abdominal myomectomy
| 3
|
[
"abdominal",
"myomectomy"
] |
[
1,
1
] |
NCT02115685
|
1:25:chronic_disease
|
heterotopic ossification
| 3
|
[
"heterotopic",
"ossification"
] |
[
2,
2
] |
NCT02405078
|
156:159:treatment,182:193:chronic_disease,203:224:chronic_disease
|
Any condition that, in the opinion of the investigator, would interfere with the interpretation of study results or subject safety including non-malignant FDG avid diseases such as sarcoidosis or other granulomatous disease
| 3
|
[
"Any",
"condition",
"that",
",",
"in",
"the",
"opinion",
"of",
"the",
"investigator",
",",
"would",
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"with",
"the",
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"of",
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"results",
"or",
"subject",
"safety",
"including",
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"FDG",
"avid",
"diseases",
"such",
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"or",
"other",
"granulomatous",
"disease"
] |
[
0,
0,
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0,
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0,
0,
0,
0,
2,
0,
0,
2,
2
] |
NCT02253316
|
1:25:chronic_disease
|
unstable angina pectoris
| 3
|
[
"unstable",
"angina",
"pectoris"
] |
[
2,
2,
2
] |
NCT03137758
|
8:25:treatment,30:45:cancer,,68:77:treatment
|
use of opiate analgesics for prostate cancer pain within 4 week of treatment start
| 3
|
[
"use",
"of",
"opiate",
"analgesics",
"for",
"prostate",
"cancer",
"pain",
"within",
"4",
"week",
"of",
"treatment",
"start"
] |
[
0,
0,
1,
1,
0,
3,
3,
0,
0,
0,
0,
0,
1,
0
] |
NCT02549833
|
62:66:chronic_disease,68:86:chronic_disease,101:109:chronic_disease,111:124:chronic_disease
|
Any conditions that could potentially alter immune function (AIDS, multiple sclerosis, uncontrolled diabetes, renal failure)
| 3
|
[
"Any",
"conditions",
"that",
"could",
"potentially",
"alter",
"immune",
"function",
"(",
"AIDS",
",",
"multiple",
"sclerosis",
",",
"uncontrolled",
"diabetes",
",",
"renal",
"failure",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
2,
2,
0,
0,
2,
0,
2,
2,
0
] |
NCT02579044
|
16:29:treatment
|
ho may require major surgery during the course of the study
| 3
|
[
"ho",
"may",
"require",
"major",
"surgery",
"during",
"the",
"course",
"of",
"the",
"study"
] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT02501096
|
,,114:124:treatment
|
Must be on a stable dose of the same oral hormonal contraceptive product for at least 4 weeks before dosing with study drug and for the duration of the study
| 3
|
[
"Must",
"be",
"on",
"a",
"stable",
"dose",
"of",
"the",
"same",
"oral",
"hormonal",
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"product",
"for",
"at",
"least",
"4",
"weeks",
"before",
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"drug",
"and",
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0,
0,
0,
0,
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0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT01943851
|
,87:102:treatment,93:102:treatment,189:198:treatment
|
Female subjects who are lactating must discontinue nursing prior to the first dose of study treatment and must refrain from nursing throughout the treatment period and for 5 half-lives of GSK525762
| 3
|
[
"Female",
"subjects",
"who",
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"lactating",
"must",
"discontinue",
"nursing",
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0,
0,
0,
0,
0,
0,
1
] |
NCT02519452
|
1:30:cancer,,,,
|
immunoglobulin (Ig) G myeloma (serum monoclonal paraprotein [M-protein] level >=1.0 gram/deciliter [g/dL] or urine M-protein level greater than or equal to (>=) 200 milligram[mg]/24 hours[hrs]
| 3
|
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"Ig",
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"gram/deciliter",
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">",
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NCT02088554
|
1:13:treatment
|
LAA ligation
| 3
|
[
"LAA",
"ligation"
] |
[
1,
1
] |
NCT02249520
|
26:36:treatment
|
Any contraindications to MR imaging
| 3
|
[
"Any",
"contraindications",
"to",
"MR",
"imaging"
] |
[
0,
0,
0,
1,
1
] |
NCT01562626
|
17:28:treatment,36:53:treatment,64:83:treatment
|
Currently using antibiotics and/or anti fungal agent (however, topical antibiotics are permitted)
| 3
|
[
"Currently",
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"antibiotics",
"and/or",
"anti",
"fungal",
"agent",
"(",
"however",
",",
"topical",
"antibiotics",
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"permitted",
")"
] |
[
0,
0,
1,
0,
1,
1,
1,
0,
0,
0,
1,
1,
0,
0,
0
] |
NCT02043548
|
30:38:treatment,45:57:treatment,59:71:treatment,73:83:treatment,85:106:treatment
|
8 week washout for any other IS agent (e.g. azathioprine, cyclosporine, tacrolimus, mycophenolate mofetil)
| 3
|
[
"8",
"week",
"washout",
"for",
"any",
"other",
"IS",
"agent",
"(",
"e.g",
".",
"azathioprine",
",",
"cyclosporine",
",",
"tacrolimus",
",",
"mycophenolate",
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[
0,
0,
0,
0,
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0,
1,
1,
0,
0,
0,
1,
0,
1,
0,
1,
0,
1,
1,
0
] |
NCT01037790
|
47:59:cancer
|
The subject has disease that is assessable by tumor marker, physical, or radiologic means
| 3
|
[
"The",
"subject",
"has",
"disease",
"that",
"is",
"assessable",
"by",
"tumor",
"marker",
",",
"physical",
",",
"or",
"radiologic",
"means"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
0,
0,
0,
0,
0,
0
] |
NCT03135990
|
17:39:treatment,,,
|
Participants on psychiatric medication must be on a stable dose for at least 2 months prior to study participation and remain symptomatic to the level identified for study inclusion (Anxiety Disorders Interview Schedule-5 less than or equal to 4). Family agrees to refrain from med changes over the course of the study if at all possible
| 3
|
[
"Participants",
"on",
"psychiatric",
"medication",
"must",
"be",
"on",
"a",
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"dose",
"for",
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"2",
"months",
"prior",
"to",
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"Anxiety",
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"less",
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0,
0
] |
NCT01898793
|
1:12:treatment,14:26:treatment,30:39:treatment,97:106:treatment
|
CNS therapy (chemotherapy or radiation) should continue as medically indicated during the study treatment
| 3
|
[
"CNS",
"therapy",
"(",
"chemotherapy",
"or",
"radiation",
")",
"should",
"continue",
"as",
"medically",
"indicated",
"during",
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] |
[
1,
1,
0,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02278315
|
1:20:chronic_disease
|
Progressive disease
| 3
|
[
"Progressive",
"disease"
] |
[
2,
2
] |
NCT01876511
|
28:45:cancer
|
Patients with MSI negative colorectal cancer
| 3
|
[
"Patients",
"with",
"MSI",
"negative",
"colorectal",
"cancer"
] |
[
0,
0,
0,
0,
3,
3
] |
NCT02304458
|
1:28:treatment,36:57:treatment,59:68:treatment,,132:159:treatment
|
Radiopharmaceutical therapy (e.g., radiolabeled antibody, 131I-MIBG): >= 42 days must have elapsed since systemically administered radiopharmaceutical therapy
| 3
|
[
"Radiopharmaceutical",
"therapy",
"(",
"e.g.",
",",
"radiolabeled",
"antibody",
",",
"131I-MIBG",
")",
":",
">",
"=",
"42",
"days",
"must",
"have",
"elapsed",
"since",
"systemically",
"administered",
"radiopharmaceutical",
"therapy"
] |
[
1,
1,
0,
0,
0,
1,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT01795313
|
32:54:chronic_disease
|
must not have a history of any immune system disorder or laboratory abnormality or any condition that could potentially alter immune function
| 3
|
[
"must",
"not",
"have",
"a",
"history",
"of",
"any",
"immune",
"system",
"disorder",
"or",
"laboratory",
"abnormality",
"or",
"any",
"condition",
"that",
"could",
"potentially",
"alter",
"immune",
"function"
] |
[
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03085485
|
14:22:chronic_disease
|
Uncontrolled Diabetes
| 3
|
[
"Uncontrolled",
"Diabetes"
] |
[
0,
2
] |
NCT02243813
|
19:39:treatment,41:50:treatment,63:74:treatment,
|
Agree not to take sildenafil (Viagra®), tadalafil, or similar medications within 72 hours of each drug administration
| 3
|
[
"Agree",
"not",
"to",
"take",
"sildenafil",
"(",
"Viagra®",
")",
",",
"tadalafil",
",",
"or",
"similar",
"medications",
"within",
"72",
"hours",
"of",
"each",
"drug",
"administration"
] |
[
0,
0,
0,
0,
1,
1,
0,
0,
0,
1,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02106598
|
,,,53:66:chronic_disease
|
New York Heart Association Classification III or IV heart disease
| 3
|
[
"New",
"York",
"Heart",
"Association",
"Classification",
"III",
"or",
"IV",
"heart",
"disease"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
2,
2
] |
NCT02955394
|
16:29:treatment
|
Planned to get local surgery
| 3
|
[
"Planned",
"to",
"get",
"local",
"surgery"
] |
[
0,
0,
0,
1,
1
] |
NCT03137121
|
28:34:treatment
|
Not have concurrent use of ethyol
| 3
|
[
"Not",
"have",
"concurrent",
"use",
"of",
"ethyol"
] |
[
0,
0,
0,
0,
0,
1
] |
NCT02369458
|
23:29:treatment,31:35:treatment,37:46:treatment,51:57:treatment
|
Progression following platin, 5-FU, cetuximab and taxane given for incurable disease
| 3
|
[
"Progression",
"following",
"platin",
",",
"5-FU",
",",
"cetuximab",
"and",
"taxane",
"given",
"for",
"incurable",
"disease"
] |
[
0,
0,
1,
0,
1,
0,
1,
0,
1,
0,
0,
0,
0
] |
NCT02050113
|
1:27:treatment
|
Previous abdominal surgery
| 3
|
[
"Previous",
"abdominal",
"surgery"
] |
[
1,
1,
1
] |
NCT02922569
|
28:97:treatment
|
Participants enrolled in a concurrent clinical trial involving an investigational pharmaceutical
| 3
|
[
"Participants",
"enrolled",
"in",
"a",
"concurrent",
"clinical",
"trial",
"involving",
"an",
"investigational",
"pharmaceutical"
] |
[
0,
0,
0,
0,
1,
1,
1,
1,
1,
1,
1
] |
NCT03027388
|
14:34:chronic_disease,77:93:chronic_disease,107:131:chronic_disease,133:158:chronic_disease,159:177:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia
| 3
|
[
"Uncontrolled",
"intercurrent",
"illness",
"including",
",",
"but",
"not",
"limited",
"to",
",",
"ongoing",
"or",
"active",
"infection",
",",
"symptomatic",
"congestive",
"heart",
"failure",
",",
"unstable",
"angina",
"pectoris",
",",
"cardiac",
"arrhythmia"
] |
[
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
2,
2,
2,
0,
2,
2,
2,
0,
2,
2
] |
NCT03028831
|
1:14:chronic_disease
|
malabsorption
| 3
|
[
"malabsorption"
] |
[
2
] |
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