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NCT01990209
|
12:33:chronic_disease,56:78:chronic_disease,,,213:234:chronic_disease,240:260:chronic_disease,262:280:chronic_disease,297:319:chronic_disease,335:352:chronic_disease,358:405:chronic_disease,,446:456:treatment
|
History of myocardial infarction, unstable symptomatic ischemic heart disease, ongoing arrhythmias > Grade 2 (National Cancer Institute [NCI] Common Terminology Criteria for Adverse Events [CTCAE], Version 4.0), thromboembolic events (eg, deep vein thrombosis, pulmonary embolism, or symptomatic cerebrovascular events), or any other cardiac condition (eg, pericardial effusion restrictive cardiomyopathy) within 6 months prior to first dose of study drug
| 3
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NCT02342782
|
31:49:treatment,59:63:cancer,137:174:cancer,179:183:cancer
|
First remission after initial first-line therapy (CR1) in PTCL patients, except for anaplastic lymphoma receptor tyrosine kinase (ALK)+ anaplastic large cell lymphoma (ALCL) and CTCL
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NCT02108860
|
7:16:chronic_disease,22:56:chronic_disease,58:69:chronic_disease,85:96:chronic_disease
|
Known infection with human immunodeficiency virus (HIV), hepatitis C, or a positive hepatitis B surface antigen
| 3
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NCT01684904
|
12:23:treatment,,
|
the use of transfusion or other intervention to achieve Hgb ≥ 8.0 is acceptable
| 3
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NCT02091141
|
13:35:chronic_disease,,72:87:chronic_disease,,111:132:chronic_disease,137:161:chronic_disease,,207:216:treatment,218:237:chronic_disease,242:257:chronic_disease
|
Significant cardiovascular disease, such as New York Heart Association cardiac disease (Class II or greater), myocardial infarction, or cerebrovascular accident within 3 months prior to initiation of study treatment, unstable arrhythmia, or unstable angina
| 3
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NCT00368355
|
35:64:chronic_disease,,
|
Patients with pre-existing severe restrictive pulmonary disease (FVC less than 40% of predicted)
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NCT02430051
|
13:29:chronic_disease
|
Significant motor impairment
| 3
|
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[
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NCT02513797
|
34:67:treatment,76:96:treatment,98:118:treatment,122:154:treatment
|
Documented presence of implanted congenital defect closure devices, (e.g., atrial septal defect, patent foramen ovale or ventricular septal defect device)
| 3
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NCT02811679
|
32:45:chronic_disease,54:62:chronic_disease,64:71:chronic_disease,73:80:chronic_disease,81:88:chronic_disease,90:99:chronic_disease,101:122:chronic_disease,124:142:chronic_disease,144:166:chronic_disease,168:177:chronic_disease
|
History of or current relevant CNS pathology such as epilepsy, seizure, paresis,aphasia, apoplexia, severe brain injuries, cerebellar disease, organic brain syndrome, psychosis
| 3
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NCT02344355
|
14:34:chronic_disease,77:93:chronic_disease,143:152:treatment,166:190:chronic_disease,192:216:chronic_disease,218:236:chronic_disease,241:260:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection that would result in a hospital stay or delay of treatment, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements or impact patient safety
| 3
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NCT02484404
|
23:32:treatment,23:47:treatment,69:114:cancer
|
Patients who have had treatment with docetaxel for the treatment of metastatic castrate-sensitive prostate cancer
| 3
|
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NCT02460835
|
21:42:treatment
|
contraindication to contrast-enhanced MRI
| 3
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NCT03104725
|
18:21:allergy_name
|
Known allergy to NAC
| 3
|
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0,
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NCT02166905
|
38:56:cancer,58:72:cancer,85:105:cancer,112:124:treatment,156:180:cancer
|
Eligible patients will be women with epithelial ovarian, fallopian tube, or primary peritoneal carcinoma after chemotherapy with no evidence of disease or minimal residual disease for primary or recurrent disease; this may or may not be measurable; these patients would normally enter a period of observation after standard management
| 3
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NCT02476786
|
7:10:chronic_disease,37:59:treatment,123:142:treatment
|
Known HIV-positivity on combination antiretroviral therapy because of the potential for pharmacokinetic interactions with endocrine therapies
| 3
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NCT02159560
|
17:35:treatment,
|
Expected use of epidural analgesia for >24 hours
| 3
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NCT02433158
|
25:28:chronic_disease
|
Documented diagnosis of SCD
| 3
|
[
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[
0,
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2
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NCT03113695
|
1:14:treatment,
|
Major surgery within 4 weeks prior to the start of treatment
| 3
|
[
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NCT02442323
|
1:15:cancer
|
adenocarcinoma subtypes
| 3
|
[
"adenocarcinoma",
"subtypes"
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[
3,
0
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NCT03042689
|
11:17:chronic_disease,
|
new-onset angina within 3 months before randomization
| 3
|
[
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NCT02131389
|
4:9:chronic_disease,,
|
Is Obese: (Defined for this study as having a BMI>45)
| 3
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NCT02326818
|
11:37:treatment
|
Receiving botulinum toxin injections under 85-N-0195
| 3
|
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NCT02531295
|
31:45:chronic_disease
|
Screening TSH consistent with hypothyroidism
| 3
|
[
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0,
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NCT02498951
|
68:88:cancer
|
Clinical evidence of extra-central nervous system (CNS) (systemic) non-Hodgkin lymphoma
| 3
|
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NCT01720836
|
62:95:cancer
|
Subjects must have histologically or cytologically confirmed non-small cell lung cancer (NSCLC
| 3
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NCT02047721
|
12:40:chronic_disease,42:59:chronic_disease,61:86:chronic_disease,98:113:chronic_disease,115:128:chronic_disease,130:145:chronic_disease
|
history of cardiovascular disease (CVD), diabetes mellitus, uncontrolled hypertension, untreated thyroid disease, renal disease, hepatic disease, or any other medical condition affecting weight or energy metabolism
| 3
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NCT02582827
|
98:126:treatment,165:198:treatment,200:245:treatment,250:273:treatment,
|
Transfusion of blood products [red blood cells (RBC), white blood cells (WBC) or whole blood] or Hematopoietic growth factors or other hematologic support, such as erythropoiesis-stimulating agents, granulocyte-colony stimulating factor (G-CSF), or platelet transfusion(s) within 14 days of screening
| 3
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NCT02430077
|
36:39:allergy_name
|
Hypersensitivity or intolerance to OCA or any components of its formulation
| 3
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NCT02798458
|
12:26:chronic_disease,28:50:chronic_disease,62:83:chronic_disease
|
History of diverticulitis, diverticular stricture, and other intestinal strictures
| 3
|
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2,
2,
0,
0,
0,
2,
2
] |
NCT02152995
|
14:34:chronic_disease,77:93:chronic_disease,107:131:chronic_disease,142:157:chronic_disease,167:177:chronic_disease,182:201:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
| 3
|
[
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NCT01941316
|
18:31:treatment,
|
Must have had no major surgery within 28 days prior to enrollment
| 3
|
[
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NCT01508390
|
23:53:cancer
|
Histologically proven adenocarcinoma of the prostate
| 3
|
[
"Histologically",
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"adenocarcinoma",
"of",
"the",
"prostate"
] |
[
0,
0,
3,
3,
3,
3
] |
NCT02120222
|
1:27:chronic_disease
|
inflammatory bowel disease
| 3
|
[
"inflammatory",
"bowel",
"disease"
] |
[
2,
2,
2
] |
NCT02577549
|
120:129:chronic_disease,131:146:chronic_disease,155:178:chronic_disease
|
Significant co-morbid disease that would threaten safety or impair ability to participate in interventions or testing (Blindness; Type 1 diabetes; Severe coronary artery disease)
| 3
|
[
"Significant",
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"disease",
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2,
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2,
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0,
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2,
2,
0
] |
NCT03043794
|
102:116:treatment
|
Subjects without placement of a biopsy clip at the diagnostic procedure who are unwilling to undergo clip placement
| 3
|
[
"Subjects",
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0,
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0,
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0
] |
NCT01616108
|
8:21:chronic_disease
|
Active eye infection
| 3
|
[
"Active",
"eye",
"infection"
] |
[
0,
2,
2
] |
NCT02531880
|
21:56:chronic_disease
|
Personal history of Parkinson s Disease or Parkinsonism or presence of this disease in a 1st degree relative
| 3
|
[
"Personal",
"history",
"of",
"Parkinson",
"s",
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"or",
"presence",
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0,
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0,
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0,
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] |
NCT01547429
|
84:92:chronic_disease,94:108:treatment,117:129:chronic_disease,131:146:chronic_disease,170:184:chronic_disease
|
Abnormality of the iris or ocular structure which would preclude fixation, such as aniridia, hemiiridectomy, severe iris atrophy, rubeosis iridis, or other compromising iris pathology
| 3
|
[
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2,
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0,
0,
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] |
NCT02496611
|
1:27:treatment
|
Previous bariatric surgery
| 3
|
[
"Previous",
"bariatric",
"surgery"
] |
[
1,
1,
1
] |
NCT03105362
|
20:34:treatment,
|
Patients receiving IV antibiotics within the previous 72h
| 3
|
[
"Patients",
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"within",
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] |
[
0,
0,
1,
1,
0,
0,
0,
0
] |
NCT02968602
|
,22:31:treatment,35:57:treatment,,96:109:treatment,111:126:treatment,128:144:treatment,146:169:treatment
|
Less than two months treatment of adjunctive medications AND less than one month on same dose: beta blockers, antidepressants, mood stabilizers, antianxiety medications
| 3
|
[
"Less",
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"months",
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1,
0,
1,
0,
1,
1,
0,
1,
1
] |
NCT02665338
|
12:22:chronic_disease
|
History of autoimmune
| 3
|
[
"History",
"of",
"autoimmune"
] |
[
0,
0,
2
] |
NCT03104699
|
48:74:cancer
|
Subjects must have recurrent, unresectable, or metastatic cervical cancer
| 3
|
[
"Subjects",
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",",
"unresectable",
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0,
0,
0,
0,
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3,
3,
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] |
NCT01697865
|
10:28:chronic_disease
|
Previous shoulder infection
| 3
|
[
"Previous",
"shoulder",
"infection"
] |
[
0,
2,
2
] |
NCT02250157
|
31:42:treatment,60:69:treatment,79:89:cancer
|
Are currently receiving other medications intended for the treatment of their malignancy
| 3
|
[
"Are",
"currently",
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"other",
"medications",
"intended",
"for",
"the",
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[
0,
0,
0,
0,
1,
0,
0,
0,
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0,
0,
3
] |
NCT01942018
|
1:33:treatment
|
Prior esophageal Botox injection
| 3
|
[
"Prior",
"esophageal",
"Botox",
"injection"
] |
[
1,
1,
1,
1
] |
NCT02549833
|
41:49:treatment,74:93:treatment,113:128:cancer
|
must show supratentorial, non-enhancing T2-FLAIR lesions that need to be surgically resected and are likely WHO grade II glioma
| 3
|
[
"must",
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",",
"non-enhancing",
"T2-FLAIR",
"lesions",
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0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
3,
3,
3
] |
NCT02189889
|
32:40:allergy_name
|
have known hypersensitivity to Feraheme or any of its components
| 3
|
[
"have",
"known",
"hypersensitivity",
"to",
"Feraheme",
"or",
"any",
"of",
"its",
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] |
[
0,
0,
0,
0,
4,
0,
0,
0,
0,
0
] |
NCT03122912
|
1:7:treatment,
|
Lovaza™ (prescription fish oil) and not willing to go off Lovaza for 3 weeks prior to enrollment to end of study
| 3
|
[
"Lovaza™",
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"fish",
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0,
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0,
0,
0,
0
] |
NCT02519322
|
52:71:allergy_name
|
History of severe hypersensitivity reaction to any monoclonal antibody
| 3
|
[
"History",
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"severe",
"hypersensitivity",
"reaction",
"to",
"any",
"monoclonal",
"antibody"
] |
[
0,
0,
0,
0,
0,
0,
0,
4,
4
] |
NCT02271919
|
19:33:chronic_disease,40:47:chronic_disease,51:71:chronic_disease,,,122:135:chronic_disease,,
|
History of severe kidney disease (e.g. chronic or acute kidney failure) with creatinine clearance below 30 and/or severe liver disease with liver tests over 4 times the upper normal level
| 3
|
[
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"severe",
"kidney",
"disease",
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"e.g",
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"chronic",
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] |
NCT02562235
|
1:33:chronic_disease
|
Pulmonary veno-occlusive disease
| 3
|
[
"Pulmonary",
"veno-occlusive",
"disease"
] |
[
2,
2,
2
] |
NCT02503709
|
1:35:chronic_disease,31:34:chronic_disease,57:91:treatment,115:129:treatment,,
|
Human immunodeficiency virus (HIV)-positive patients on combination antiretroviral therapy known to interact with CYP isoenzymes are ineligible; in addition, HIV patients with CD4 count < 200 cells/uL are ineligible; appropriate studies will be undertaken in patients receiving combination antiretroviral therapy when indicated
| 3
|
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NCT03011567
|
29:44:treatment,80:99:treatment,103:125:chronic_disease
|
Use of therapeutic doses of anticoagulation (low dose anticoagulation used for routine prophylaxis of venous thromboembolism is acceptable)
| 3
|
[
"Use",
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"therapeutic",
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[
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1,
0,
0,
0,
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1,
0,
2,
2,
0,
0,
0
] |
NCT02544880
|
14:25:chronic_disease
|
Uncontrolled arrhythmias
| 3
|
[
"Uncontrolled",
"arrhythmias"
] |
[
0,
2
] |
NCT01620216
|
11:38:chronic_disease
|
Diagnosed congenital long QT syndrome
| 3
|
[
"Diagnosed",
"congenital",
"long",
"QT",
"syndrome"
] |
[
0,
2,
2,
2,
2
] |
NCT03013543
|
1:37:chronic_disease
|
LEPR Heterozygous Deficiency Obesity
| 3
|
[
"LEPR",
"Heterozygous",
"Deficiency",
"Obesity"
] |
[
2,
2,
2,
2
] |
NCT02050113
|
4:12:chronic_disease,16:31:chronic_disease,62:90:chronic_disease
|
No systemic or local infection that may increase the risk of endovascular graft infection
| 3
|
[
"No",
"systemic",
"or",
"local",
"infection",
"that",
"may",
"increase",
"the",
"risk",
"of",
"endovascular",
"graft",
"infection"
] |
[
0,
2,
0,
2,
2,
0,
0,
0,
0,
0,
0,
2,
2,
2
] |
NCT02444689
|
15:20:chronic_disease
|
Overweight or Obese
| 3
|
[
"Overweight",
"or",
"Obese"
] |
[
0,
0,
2
] |
NCT02542202
|
35:62:treatment,66:94:treatment,102:119:treatment
|
Patients may not be receiving any systemic anti-cancer agents or other investigational agents during radiation therapy
| 3
|
[
"Patients",
"may",
"not",
"be",
"receiving",
"any",
"systemic",
"anti-cancer",
"agents",
"or",
"other",
"investigational",
"agents",
"during",
"radiation",
"therapy"
] |
[
0,
0,
0,
0,
0,
0,
1,
1,
1,
0,
1,
1,
1,
0,
1,
1
] |
NCT02568267
|
7:24:chronic_disease
|
Known active infections
| 3
|
[
"Known",
"active",
"infections"
] |
[
0,
2,
2
] |
NCT02498613
|
22:29:chronic_disease,31:54:chronic_disease,59:87:chronic_disease,
|
History of abdominal fistula, intra-abdominal abscess, or gastrointestinal perforation within the 3 months prior to enrollment
| 3
|
[
"History",
"of",
"abdominal",
"fistula",
",",
"intra-abdominal",
"abscess",
",",
"or",
"gastrointestinal",
"perforation",
"within",
"the",
"3",
"months",
"prior",
"to",
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] |
[
0,
0,
0,
2,
0,
2,
2,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT03125902
|
5:8:chronic_disease,
|
The HBV DNA test will be performed only for patients who have a positive HBcAb test
| 3
|
[
"The",
"HBV",
"DNA",
"test",
"will",
"be",
"performed",
"only",
"for",
"patients",
"who",
"have",
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[
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02418195
|
23:40:treatment
|
capable of undergoing ketamine infusion
| 3
|
[
"capable",
"of",
"undergoing",
"ketamine",
"infusion"
] |
[
0,
0,
0,
1,
1
] |
NCT02236013
|
,,124:134:treatment
|
Female subject must not donate ova starting at Screening and throughout the study period, and for 180 days after the final study drug administration
| 3
|
[
"Female",
"subject",
"must",
"not",
"donate",
"ova",
"starting",
"at",
"Screening",
"and",
"throughout",
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"study",
"period",
",",
"and",
"for",
"180",
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"after",
"the",
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1,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02642939
|
27:40:treatment,
|
Patients who have had any major surgery within 4 weeks prior to day 1 of cycle 1
| 3
|
[
"Patients",
"who",
"have",
"had",
"any",
"major",
"surgery",
"within",
"4",
"weeks",
"prior",
"to",
"day",
"1",
"of",
"cycle",
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[
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03181516
|
1:20:treatment
|
Keflex (cephalexin)
| 3
|
[
"Keflex",
"(",
"cephalexin",
")"
] |
[
1,
1,
0,
0
] |
NCT01620216
|
1:26:chronic_disease
|
Uncontrolled hypertension
| 3
|
[
"Uncontrolled",
"hypertension"
] |
[
2,
2
] |
NCT02943408
|
17:53:chronic_disease
|
Other Specified Trauma and Stressor-Related Disorder (309.89)
| 3
|
[
"Other",
"Specified",
"Trauma",
"and",
"Stressor-Related",
"Disorder",
"(",
"309.89",
")"
] |
[
0,
0,
2,
2,
2,
2,
0,
0,
0
] |
NCT02400255
|
,60:67:treatment,,,108:129:treatment,,,165:185:treatment,
|
Adequate engraftment within 7 days prior to starting study therapy: ANC ≥ 1.0 x 109/L without daily use of myeloid growth factor; and platelet ≥ 25 x 109/L without platelet transfusion within 1 week
| 3
|
[
"Adequate",
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0,
0,
0,
0,
0,
1,
1,
1,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01969643
|
1:22:cancer
|
Malignant CNS disease that has not been definitively treated
| 3
|
[
"Malignant",
"CNS",
"disease",
"that",
"has",
"not",
"been",
"definitively",
"treated"
] |
[
3,
3,
3,
0,
0,
0,
0,
0,
0
] |
NCT01850758
|
23:26:treatment
|
Contraindications for MRI
| 3
|
[
"Contraindications",
"for",
"MRI"
] |
[
0,
0,
1
] |
NCT02518594
|
12:18:chronic_disease
|
History of herpes
| 3
|
[
"History",
"of",
"herpes"
] |
[
0,
0,
2
] |
NCT03135522
|
1:25:chronic_disease
|
Congestive heart failure
| 3
|
[
"Congestive",
"heart",
"failure"
] |
[
2,
2,
2
] |
NCT02724540
|
1:12:cancer,,
|
liver tumor burden less than or equal to 70% of the total liver volume by visual estimate
| 3
|
[
"liver",
"tumor",
"burden",
"less",
"than",
"or",
"equal",
"to",
"70",
"%",
"of",
"the",
"total",
"liver",
"volume",
"by",
"visual",
"estimate"
] |
[
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02215096
|
13:48:treatment,59:79:treatment,,153:162:treatment
|
Presence of hepatitis B surface antigen (HBsAg), positive hepatitis C antibody test result at screening or within 3 months prior to first dose of study treatment
| 3
|
[
"Presence",
"of",
"hepatitis",
"B",
"surface",
"antigen",
"(",
"HBsAg",
")",
",",
"positive",
"hepatitis",
"C",
"antibody",
"test",
"result",
"at",
"screening",
"or",
"within",
"3",
"months",
"prior",
"to",
"first",
"dose",
"of",
"study",
"treatment"
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[
0,
0,
1,
1,
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1,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT01595529
|
1:11:treatment
|
Cephalexin
| 3
|
[
"Cephalexin"
] |
[
1
] |
NCT02759120
|
1:30:treatment,36:48:treatment,50:63:treatment,65:81:treatment,86:98:treatment
|
Concomitant immunosuppression with azathioprine, mycophenolate, cyclophosphamide, or cyclosporine
| 3
|
[
"Concomitant",
"immunosuppression",
"with",
"azathioprine",
",",
"mycophenolate",
",",
"cyclophosphamide",
",",
"or",
"cyclosporine"
] |
[
1,
1,
0,
1,
0,
1,
0,
1,
0,
0,
1
] |
NCT01604512
|
22:29:allergy_name
|
allergic reaction to Gd-DTPA
| 3
|
[
"allergic",
"reaction",
"to",
"Gd-DTPA"
] |
[
0,
0,
0,
4
] |
NCT01532687
|
48:79:cancer,102:119:cancer,145:159:cancer
|
subjects with a history of completely resected non-melanomatous skin carcinoma, successfully treated in situ carcinoma, or successfully treated bladder cancer are eligible
| 3
|
[
"subjects",
"with",
"a",
"history",
"of",
"completely",
"resected",
"non-melanomatous",
"skin",
"carcinoma",
",",
"successfully",
"treated",
"in",
"situ",
"carcinoma",
",",
"or",
"successfully",
"treated",
"bladder",
"cancer",
"are",
"eligible"
] |
[
0,
0,
0,
0,
0,
0,
0,
3,
3,
3,
0,
0,
0,
3,
3,
3,
0,
0,
0,
0,
3,
3,
0,
0
] |
NCT01366612
|
14:20:chronic_disease
|
uncontrolled angina
| 3
|
[
"uncontrolled",
"angina"
] |
[
0,
2
] |
NCT02637947
|
19:40:chronic_disease
|
subject has had a myocardial infarction
| 3
|
[
"subject",
"has",
"had",
"a",
"myocardial",
"infarction"
] |
[
0,
0,
0,
0,
2,
2
] |
NCT02163317
|
,,49:64:treatment
|
PSA should not be obtained within 10 days after prostate biopsy
| 3
|
[
"PSA",
"should",
"not",
"be",
"obtained",
"within",
"10",
"days",
"after",
"prostate",
"biopsy"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT03123068
|
1:27:treatment,,60:72:treatment,76:88:treatment
|
Immune-suppressant therapy within the last 2 months (e.g., azathioprine or cyclosporine)
| 3
|
[
"Immune-suppressant",
"therapy",
"within",
"the",
"last",
"2",
"months",
"(",
"e.g.",
",",
"azathioprine",
"or",
"cyclosporine",
")"
] |
[
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0
] |
NCT02819635
|
14:32:chronic_disease,
|
Diagnosis of ulcerative colitis for 90 days or greater prior to Baseline, confirmed by colonoscopy during the Screening Period
| 3
|
[
"Diagnosis",
"of",
"ulcerative",
"colitis",
"for",
"90",
"days",
"or",
"greater",
"prior",
"to",
"Baseline",
",",
"confirmed",
"by",
"colonoscopy",
"during",
"the",
"Screening",
"Period"
] |
[
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02031250
|
1:3:cancer,7:19:cancer,23:44:cancer
|
T3 or T4 laryngeal or hypopharyngeal cancer that is locally advanced
| 3
|
[
"T3",
"or",
"T4",
"laryngeal",
"or",
"hypopharyngeal",
"cancer",
"that",
"is",
"locally",
"advanced"
] |
[
3,
0,
3,
3,
0,
3,
3,
0,
0,
0,
0
] |
NCT02977299
|
,33:67:treatment,
|
received at least one dose of a monoamine oxidase inhibitor (MAOI) four weeks or less prior
| 3
|
[
"received",
"at",
"least",
"one",
"dose",
"of",
"a",
"monoamine",
"oxidase",
"inhibitor",
"(",
"MAOI",
")",
"four",
"weeks",
"or",
"less",
"prior"
] |
[
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02784535
|
20:38:chronic_disease
|
History of serious neurologic disease
| 3
|
[
"History",
"of",
"serious",
"neurologic",
"disease"
] |
[
0,
0,
0,
2,
2
] |
NCT02589340
|
1:33:chronic_disease
|
Significant cognitive impairment
| 3
|
[
"Significant",
"cognitive",
"impairment"
] |
[
2,
2,
2
] |
NCT01622868
|
,21:34:cancer,51:71:treatment,75:98:treatment,102:142:treatment,146:181:treatment,
|
HER2-overexpressing breast cancer (3+ staining by immunohistochemistry or HER2 gene amplification by fluorescent in situ hybridization [FISH] or silver in situ hybridization [SISH] >= 2.0)
| 3
|
[
"HER2-overexpressing",
"breast",
"cancer",
"(",
"3+",
"staining",
"by",
"immunohistochemistry",
"or",
"HER2",
"gene",
"amplification",
"by",
"fluorescent",
"in",
"situ",
"hybridization",
"[",
"FISH",
"]",
"or",
"silver",
"in",
"situ",
"hybridization",
"[",
"SISH",
"]",
">",
"=",
"2.0",
")"
] |
[
1,
1,
1,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
1,
1,
1,
1,
1,
0,
0,
0,
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT02857218
|
15:34:chronic_disease
|
Patients with renal insufficiency
| 3
|
[
"Patients",
"with",
"renal",
"insufficiency"
] |
[
0,
0,
2,
2
] |
NCT02259504
|
30:36:treatment,38:48:treatment,52:65:treatment
|
Use of other modified coils (Matrix, HydroCoil® or fibered coils)
| 3
|
[
"Use",
"of",
"other",
"modified",
"coils",
"(",
"Matrix",
",",
"HydroCoil®",
"or",
"fibered",
"coils",
")"
] |
[
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1
] |
NCT02098161
|
,,,,180:219:treatment
|
Pregnant or breast feeding (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive beta-human chorionic gonadotropin (HCG) laboratory test
| 3
|
[
"Pregnant",
"or",
"breast",
"feeding",
"(",
"lactating",
")",
"women",
",",
"where",
"pregnancy",
"is",
"defined",
"as",
"the",
"state",
"of",
"a",
"female",
"after",
"conception",
"and",
"until",
"the",
"termination",
"of",
"gestation",
",",
"confirmed",
"by",
"a",
"positive",
"beta-human",
"chorionic",
"gonadotropin",
"(",
"HCG",
")",
"laboratory",
"test"
] |
[
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,
1,
1,
0,
0,
0,
0
] |
NCT00630565
|
1:29:cancer
|
Acute myeloid leukemia (AML)
| 3
|
[
"Acute",
"myeloid",
"leukemia",
"(",
"AML",
")"
] |
[
3,
3,
3,
3,
0,
0
] |
NCT02943408
|
1:15:chronic_disease
|
panic disorder (300.01)
| 3
|
[
"panic",
"disorder",
"(",
"300.01",
")"
] |
[
2,
2,
0,
0,
0
] |
NCT02593526
|
24:43:treatment,
|
Intention to change to peritoneal dialysis, or home HD in the next 6 months
| 3
|
[
"Intention",
"to",
"change",
"to",
"peritoneal",
"dialysis",
",",
"or",
"home",
"HD",
"in",
"the",
"next",
"6",
"months"
] |
[
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01625234
|
20:68:treatment,70:93:treatment,99:120:treatment
|
Patients receiving CYP3A substrates with narrow therapeutic indices, strong CYP3A inhibitors, and strong CYP3A inducers
| 3
|
[
"Patients",
"receiving",
"CYP3A",
"substrates",
"with",
"narrow",
"therapeutic",
"indices",
",",
"strong",
"CYP3A",
"inhibitors",
",",
"and",
"strong",
"CYP3A",
"inducers"
] |
[
0,
0,
1,
1,
1,
1,
1,
1,
0,
1,
1,
1,
0,
0,
0,
0,
0
] |
NCT02058095
|
22:35:chronic_disease,,,,,
|
Patients with severe liver disease (AST > 3x normal, alkaline phosphatase or bilirubin > 2x normal)
| 3
|
[
"Patients",
"with",
"severe",
"liver",
"disease",
"(",
"AST",
">",
"3x",
"normal",
",",
"alkaline",
"phosphatase",
"or",
"bilirubin",
">",
"2x",
"normal",
")"
] |
[
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02131467
|
1:10:chronic_disease
|
hepatitis
| 3
|
[
"hepatitis"
] |
[
2
] |
NCT02500381
|
25:28:chronic_disease
|
Genotypically confirmed DMD, with genetic deletion amenable to exon 45 or exon 53 skipping
| 3
|
[
"Genotypically",
"confirmed",
"DMD",
",",
"with",
"genetic",
"deletion",
"amenable",
"to",
"exon",
"45",
"or",
"exon",
"53",
"skipping"
] |
[
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
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