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NCT01553942
|
7:10:chronic_disease
|
known HIV carrier
| 1
|
[
"known",
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"carrier"
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0,
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0
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NCT01522768
|
25:46:treatment,37:46:treatment,71:84:treatment,86:103:treatment,127:144:treatment,150:173:treatment,289:305:treatment,,363:371:treatment,,548:563:treatment
|
Additional experimental anti-cancer treatment and/or standard chemo-, immunotherapy, hormone treatment (with the exception of megestrol acetate), or concurrent radiotherapy is not allowed concomitantly with the administration of study treatment (with the exception listed in section 9.0) 89Zr-trastuzumab use as imaging agent for 89Zr-trastuzumab PET permitted. Afatinib is a substrate of P-gp and its plasma concentrations can be affected by the use of P-gp inhibitors (data on file) and it is also likely that P-gp inducers could also influence afatinib plasma concentrations
| 1
|
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NCT02393794
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19:36:chronic_disease,47:94:chronic_disease,96:115:chronic_disease,120:131:chronic_disease
|
Other significant ECG abnormalities including 2nd degree atrio-ventricular (AV) block type II, 3rd degree AV block, or bradycardia
| 1
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NCT01072370
|
1:9:chronic_disease
|
diarrhea
| 1
|
[
"diarrhea"
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[
2
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NCT02340156
|
1:6:cancer
|
Tumor foci detected below the tentorium or beyond the cranial vault
| 1
|
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NCT02395393
|
35:58:treatment
|
to be unable to safely tolerate a bronchoscopic procedure
| 1
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NCT01947673
|
22:46:chronic_disease
|
clinical evidence of congestive heart failure
| 1
|
[
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"failure"
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2
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NCT02565199
|
9:19:chronic_disease,,
|
Current depression (score more than 7 on the Hamilton Depression Rating Scale (HDRS))
| 1
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NCT02266329
|
,398:413:treatment
|
Participation in a headache support group or other activity such as meditation or yoga intended to mitigate headache or other chronic pain must be stable for at least 4 weeks prior to beginning the preliminary screening period and should be intended to be continued for the duration of the trial. Participants will be encouraged to defer enrolling in such activities until they have completed the treatment trial
| 1
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NCT02365467
|
16:26:chronic_disease,28:36:chronic_disease,41:56:chronic_disease
|
Subject has an aneurysmal, tortuous, or atherosclerotic LSA
| 1
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NCT02452697
|
68:89:treatment
|
Patients likely to have a significantly better durable response to allogeneic transplant alone (better than 60% progression free longer than 2 years)
| 1
|
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NCT02581215
|
83:95:cancer
|
Measurable disease determined using guidelines of Response Evaluation Criteria In Solid Tumors (RECIST 1.1)
| 1
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NCT03030118
|
51:68:treatment,70:86:treatment,91:112:treatment
|
The subject is currently or has been treated with immunosuppressive, immune modifying, or cytotoxic medications as listed in Section 7.2
| 1
|
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NCT01312857
|
,36:45:treatment
|
Renal function (≤ 14 days prior to treatment start)
| 1
|
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NCT02159703
|
39:62:cancer,70:80:cancer,93:105:cancer,
|
Histologically confirmed diagnosis of squamous cell carcinoma of the oropharynx, stage IVa, p16-positive on immunohistochemistry
| 1
|
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NCT02369458
|
7:10:chronic_disease,25:59:treatment,127:138:treatment,229:255:treatment
|
Known HIV-positivity on combination antiretroviral therapy because of the potential for pharmacokinetic interactions with the study drugs. In addition, these patients are at increased risk of lethal infections when treated with marrow-suppressive therapy. Appropriate studies will be undertaken in patients receiving combination antiretroviral therapy when indicated
| 1
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NCT03181516
|
1:11:treatment
|
Cephradine
| 1
|
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"Cephradine"
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[
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NCT01915095
|
20:36:chronic_disease,40:49:chronic_disease,51:75:chronic_disease
|
Premorbid, ongoing major depression or psychosis, altered cognitive status
| 1
|
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NCT01920061
|
15:19:cancer,,,41:60:treatment,68:78:cancer
|
Patients with TNBC and one or two prior cytotoxic therapies in the metastatic setting
| 1
|
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NCT01595529
|
24:44:chronic_disease
|
A child diagnosed with congenital anomalies of the genitourinary tract
| 1
|
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NCT02469857
|
21:48:chronic_disease
|
Patients with overt peripheral vascular disease in the involved area
| 1
|
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NCT02471911
|
29:48:treatment,41:48:treatment,60:69:treatment,73:90:treatment,
|
Patients who have had other anti-cancer therapy, including radiation or experimental drug or therapy, within 28 days of enrollment
| 1
|
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NCT03085485
|
1:7:chronic_disease
|
Angina symptoms
| 1
|
[
"Angina",
"symptoms"
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[
2,
0
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NCT03075761
|
1:25:chronic_disease
|
congestive heart failure
| 1
|
[
"congestive",
"heart",
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[
2,
2,
2
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NCT02442622
|
12:38:treatment
|
History of cortical steroid injection to affected wrist and/or thumb
| 1
|
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NCT02582775
|
,,93:103:treatment
|
Cardiac: left ventricular ejection fraction ≥ 45%, normal EKG or approved by Cardiology for transplant
| 1
|
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NCT02579044
|
23:31:chronic_disease
|
Genetically-confirmed progeria
| 1
|
[
"Genetically-confirmed",
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[
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2
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NCT02847689
|
1:21:chronic_disease
|
Congenital anomalies
| 1
|
[
"Congenital",
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[
2,
2
] |
NCT02574910
|
1:40:chronic_disease,52:77:chronic_disease,133:152:treatment
|
Concurrent medical condition or disease other than 21-hydroxylase deficiency that may interfere with linear growth or that requires concomitant therapy that is likely to interfere with study procedures or results
| 1
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NCT02378714
|
,,171:181:treatment,
|
women of childbearing potential must agree to use a medically acceptable method of birth control or abstain from sexual intercourse during the time they are taking study medication and for at least one month after the medication period ends
| 1
|
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NCT02488967
|
12:35:cancer,48:63:cancer,80:94:treatment,99:109:cancer,114:150:cancer,
|
History of non-breast malignancies (except for in situ cancers treated only by local excision and basal cell and squamous cell carcinomas of the skin) within 5 years prior to randomization
| 1
|
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NCT02513485
|
23:32:chronic_disease,34:42:chronic_disease,44:52:cancer,57:74:chronic_disease
|
Current or history of migraines, glaucoma, melanoma, or bleeding disorder of any kind
| 1
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NCT01943851
|
1:22:treatment,
|
Chemotherapy regimens given continuously or on a weekly basis with limited potential for delayed toxicity within the last 2 weeks
| 1
|
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NCT02548351
|
40:61:chronic_disease,70:93:chronic_disease,95:106:chronic_disease,108:119:chronic_disease,121:124:chronic_disease,126:129:chronic_disease,131:151:chronic_disease,153:167:chronic_disease,169:182:chronic_disease,184:214:chronic_disease,216:241:chronic_disease,262:292:cancer
|
Evidence of other known forms of known chronic liver disease such as alcoholic liver disease, hepatitis B, hepatitis C, PBC, PSC, autoimmune hepatitis, Wilson disease, iron overload, alpha-1-antitrypsin deficiency, drug-induced liver injury, known or suspected hepatocellular carcinoma (HCC)
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NCT02094118
|
8:27:treatment
|
Use of home oxygen therapy
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NCT03078491
|
1:30:chronic_disease,,
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End stage renal insufficiency (eGFR<30)
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NCT02101944
|
98:105:cancer
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Evidence of any end organ damage criteria listed below (at any time) attributed to the patient's myeloma
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NCT01185132
|
1:31:cancer,
|
Microscopic multifocal disease is only allowed when the entire span of identified disease measures 3.0 cm or less
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NCT01648751
|
31:39:chronic_disease,46:53:treatment,55:59:treatment
|
Other prior interventions for prolapse (e.g. pessary, PFPT)
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NCT01532687
|
,,17:41:chronic_disease,
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Class III or IV congestive heart failure, as defined by the New York Heart Association (NYHA)
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NCT03080844
|
5:39:chronic_disease
|
Any neurologic or psychiatric disorder
| 1
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NCT03088709
|
,78:90:treatment
|
Less than twenty-one days have elapsed since the subject's last radiation or chemotherapy prior to conditioning
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NCT02496208
|
,,,,,191:200:treatment
|
The subject has prothrombin time (PT)/international normalized ratio (INR) or partial thromboplastin time (PTT) test >= 1.5 x the laboratory ULN within 7 days before the first dose of study treatment
| 1
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NCT02334579
|
18:48:treatment
|
High risk group: three hormone therapy regimens
| 1
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NCT02472223
|
1:12:treatment,
|
Eye surgery in the last 3 months
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NCT01873131
|
56:65:treatment
|
Willingness of parent/guardian to receive EXPERIMENTAL treatment
| 1
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[
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0,
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1
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NCT03021486
|
1:9:chronic_disease
|
Delirium as per DSM-V criteria (The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5))
| 1
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NCT03063892
|
1:23:treatment
|
Active hormone therapy
| 1
|
[
"Active",
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[
1,
1,
1
] |
NCT02176161
|
1:13:treatment
|
Chemotherapy
| 1
|
[
"Chemotherapy"
] |
[
1
] |
NCT02261519
|
12:18:cancer,,68:88:cancer,93:116:cancer
|
History of cancer not in remission for the last 3 years except for basal cell carcinoma and squamous cell carcinoma
| 1
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NCT02076906
|
1:26:treatment
|
Stem Cell Transplantation
| 1
|
[
"Stem",
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[
1,
1,
1
] |
NCT01697371
|
1:13:treatment,30:43:treatment,,88:97:treatment,,,,
|
Chemotherapy and/or targeted agent therapy must be completed at least 2 weeks prior to radiation and started at least 14 days after completion of SBPT Women of childbearing potential and male participants must practice adequate contraception
| 1
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NCT02474199
|
1:11:treatment,16:29:chronic_disease,43:61:chronic_disease
|
Transplant for liver disease secondary to autoimmune disease
| 1
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NCT02544503
|
8:24:treatment
|
Use of CNS active drugs
| 1
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[
0,
0,
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1,
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NCT02074436
|
,,17:41:cancer
|
Age > 18 with a hematological malignancy
| 1
|
[
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[
0,
0,
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0,
0,
3,
3
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NCT01581580
|
18:20:chronic_disease
|
The diagnosis of ET will be confirmed on clinical examination in the NIH Movement Disorders Clinic (the diagnosis of ET will be based on bilateral
| 1
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NCT02430077
|
45:62:treatment,
|
Use of drugs which can potentially decrease hepatic steatosis during previous 3 months
| 1
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NCT02481765
|
1:11:treatment
|
Normal EEG
| 1
|
[
"Normal",
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[
1,
1
] |
NCT02245841
|
78:86:chronic_disease
|
Although not mandatory, patients with evidence of current or previous active myositis
| 1
|
[
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NCT02543983
|
21:30:chronic_disease,58:71:chronic_disease,85:103:chronic_disease
|
Presence of current psychotic features or a diagnosis of Schizophrenia or any other psychotic disorder as defined in the DSM-IV
| 1
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NCT02932410
|
,41:64:treatment
|
Subjects receiving a combination of > 2 PAH-specific treatments at randomization
| 1
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NCT01989546
|
23:63:treatment
|
Patients who have had prior treatment with any PARP inhibitors are ineligible
| 1
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NCT02771626
|
1:17:chronic_disease,39:50:treatment,52:62:treatment,67:78:treatment,,117:127:treatment
|
Active infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks prior to first dose of study drug
| 1
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[
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NCT01059786
|
1:12:chronic_disease,,
|
Neutropenia (ANC less than 1000 cells/microl)
| 1
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NCT01494662
|
44:55:chronic_disease,,,
|
In cohort 1, patients must have measurable CNS disease, defined as at least one parenchymal brain lesion that can be accurately measured in at least one dimension with longest dimension ≥10 mm by local radiology review
| 1
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NCT01525901
|
1:26:chronic_disease
|
intracranial hypertension
| 1
|
[
"intracranial",
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[
2,
2
] |
NCT01849146
|
,34:47:treatment,49:67:treatment,75:82:treatment,84:102:treatment,104:115:treatment
|
2 weeks from administration of a non-cytotoxic, FDA-approved agent (e.g., Tarceva, hydroxychloroquine, bevacizumab, etc.)
| 1
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NCT01912651
|
,39:46:treatment,48:67:treatment,93:104:treatment,109:119:treatment,147:167:cancer,208:232:treatment
|
current or recent (within one week of surgery) systemic antibiotic use, intolerance to both clindamycin and cephalexin, discovery of a persistent cutaneous malignancy at the site of the defect following the reconstructive procedure and previous reconstruction at the site of the skin/soft-tissue defect
| 1
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NCT02421315
|
30:48:chronic_disease
|
DSM-IV lifetime diagnosis of psychotic disorder
| 1
|
[
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[
0,
0,
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0,
2,
2
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NCT02320292
|
39:55:chronic_disease
|
Serious non-malignant disease such as active infection or other condition which in the opinion of the investigator would compromise other protocol objectives
| 1
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[
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01269853
|
,,124:133:treatment
|
Patients must agree to use a medically effective method of contraception during and for a period of three months after the treatment period
| 1
|
[
"Patients",
"must",
"agree",
"to",
"use",
"a",
"medically",
"effective",
"method",
"of",
"contraception",
"during",
"and",
"for",
"a",
"period",
"of",
"three",
"months",
"after",
"the",
"treatment",
"period"
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0
] |
NCT03016351
|
1:12:chronic_disease,
|
Head injury within last 6 months
| 1
|
[
"Head",
"injury",
"within",
"last",
"6",
"months"
] |
[
2,
2,
0,
0,
0,
0
] |
NCT02908906
|
9:29:treatment
|
limited palliative radiation
| 1
|
[
"limited",
"palliative",
"radiation"
] |
[
0,
1,
1
] |
NCT01668563
|
17:25:chronic_disease,64:72:treatment,76:98:treatment
|
The patient and aneurysm are considered appropriate for either surgical or endovascular treatment by the treating team
| 1
|
[
"The",
"patient",
"and",
"aneurysm",
"are",
"considered",
"appropriate",
"for",
"either",
"surgical",
"or",
"endovascular",
"treatment",
"by",
"the",
"treating",
"team"
] |
[
0,
0,
0,
2,
0,
0,
0,
0,
0,
1,
0,
1,
1,
0,
0,
0,
0
] |
NCT01660607
|
,,22:54:chronic_disease
|
Complex karyotype(≥3 clonal chromosomal abnormalities)
| 1
|
[
"Complex",
"karyotype",
"(",
"≥3",
"clonal",
"chromosomal",
"abnormalities",
")"
] |
[
0,
0,
0,
0,
2,
2,
2,
0
] |
NCT02464878
|
19:45:treatment,
|
Administration of live attenuated vaccine(s) within 2 months of enrollment
| 1
|
[
"Administration",
"of",
"live",
"attenuated",
"vaccine",
"(",
"s",
")",
"within",
"2",
"months",
"of",
"enrollment"
] |
[
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02408120
|
21:36:chronic_disease
|
Clinically relevant hepatic disease
| 1
|
[
"Clinically",
"relevant",
"hepatic",
"disease"
] |
[
0,
0,
2,
2
] |
NCT02564744
|
42:47:cancer
|
The following participants with relapsed DLBCL will be enrolled
| 1
|
[
"The",
"following",
"participants",
"with",
"relapsed",
"DLBCL",
"will",
"be",
"enrolled"
] |
[
0,
0,
0,
0,
0,
3,
0,
0,
0
] |
NCT02907944
|
27:30:chronic_disease,
|
Employed at participating HIV clinic for at least 6 months
| 1
|
[
"Employed",
"at",
"participating",
"HIV",
"clinic",
"for",
"at",
"least",
"6",
"months"
] |
[
0,
0,
0,
2,
0,
0,
0,
0,
0,
0
] |
NCT00695214
|
12:20:allergy_name,22:33:allergy_name,35:47:allergy_name,51:59:allergy_name
|
Allergy to propofol, soybean oil, egg lecithin or glycerol
| 1
|
[
"Allergy",
"to",
"propofol",
",",
"soybean",
"oil",
",",
"egg",
"lecithin",
"or",
"glycerol"
] |
[
0,
0,
4,
0,
4,
4,
0,
4,
4,
0,
4
] |
NCT01815359
|
70:80:treatment
|
Any condition that would preclude the ability to deliver appropriate IP therapy
| 1
|
[
"Any",
"condition",
"that",
"would",
"preclude",
"the",
"ability",
"to",
"deliver",
"appropriate",
"IP",
"therapy"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02982226
|
12:29:treatment
|
History of radiation therapy of the affected foot
| 1
|
[
"History",
"of",
"radiation",
"therapy",
"of",
"the",
"affected",
"foot"
] |
[
0,
0,
1,
1,
0,
0,
0,
0
] |
NCT02584309
|
,147:154:treatment,
|
measurable disease defined as lesions that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 10 mm with CT scan, as ≥ 20 mm by chest x-ray, or ≥ 10 mm with calipers by clinical exam
| 1
|
[
"measurable",
"disease",
"defined",
"as",
"lesions",
"that",
"can",
"be",
"accurately",
"measured",
"in",
"at",
"least",
"one",
"dimension",
"(",
"longest",
"diameter",
"to",
"be",
"recorded",
")",
"as",
"≥",
"10",
"mm",
"with",
"CT",
"scan",
",",
"as",
"≥",
"20",
"mm",
"by",
"chest",
"x-ray",
",",
"or",
"≥",
"10",
"mm",
"with",
"calipers",
"by",
"clinical",
"exam"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
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0,
0,
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0,
0,
0,
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0,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01422746
|
23:31:chronic_disease,,,,
|
Previous diagnosis of diabetes, fasting glucose ≥126 mg/dL, or a hemoglobin A1c ≥6.5%
| 1
|
[
"Previous",
"diagnosis",
"of",
"diabetes",
",",
"fasting",
"glucose",
"≥126",
"mg/dL",
",",
"or",
"a",
"hemoglobin",
"A1c",
"≥6.5",
"%"
] |
[
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00678145
|
15:39:chronic_disease
|
Patients with type 1 diabetes mellitus
| 1
|
[
"Patients",
"with",
"type",
"1",
"diabetes",
"mellitus"
] |
[
0,
0,
2,
2,
2,
2
] |
NCT01799135
|
26:52:cancer
|
Histologically confirmed non-small cell lung cancer
| 1
|
[
"Histologically",
"confirmed",
"non-small",
"cell",
"lung",
"cancer"
] |
[
0,
0,
3,
3,
3,
3
] |
NCT02578641
|
1:35:chronic_disease
|
Human Immunodeficiency Virus (HIV) negative
| 1
|
[
"Human",
"Immunodeficiency",
"Virus",
"(",
"HIV",
")",
"negative"
] |
[
2,
2,
2,
2,
0,
0,
0
] |
NCT01422746
|
1:18:chronic_disease
|
Hyperandrogenemic
| 1
|
[
"Hyperandrogenemic"
] |
[
2
] |
NCT02566395
|
1:4:chronic_disease
|
HIV positive
| 1
|
[
"HIV",
"positive"
] |
[
2,
0
] |
NCT02522468
|
7:20:cancer
|
Prior breast cancer on ipsilateral side
| 1
|
[
"Prior",
"breast",
"cancer",
"on",
"ipsilateral",
"side"
] |
[
0,
3,
3,
0,
0,
0
] |
NCT02323945
|
42:51:chronic_disease,53:75:chronic_disease,101:122:chronic_disease,133:141:chronic_disease,158:181:chronic_disease
|
Concurrent severe medical illness (i.e., infection, cardiovascular disease, ossification, recurrent autonomic dysreflexia, unhealed decubiti, and history of pulmonary complications)
| 1
|
[
"Concurrent",
"severe",
"medical",
"illness",
"(",
"i.e.",
",",
"infection",
",",
"cardiovascular",
"disease",
",",
"ossification",
",",
"recurrent",
"autonomic",
"dysreflexia",
",",
"unhealed",
"decubiti",
",",
"and",
"history",
"of",
"pulmonary",
"complications",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
2,
0,
2,
2,
0,
0,
0,
0,
2,
2,
0,
0,
2,
0,
0,
0,
0,
2,
2,
0
] |
NCT02503358
|
,94:103:treatment,
|
Estimated life expectancy, in the judgment of the investigator, which will permit receipt of treatment of 12 weeks or more
| 1
|
[
"Estimated",
"life",
"expectancy",
",",
"in",
"the",
"judgment",
"of",
"the",
"investigator",
",",
"which",
"will",
"permit",
"receipt",
"of",
"treatment",
"of",
"12",
"weeks",
"or",
"more"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT02278315
|
1:16:treatment,40:60:treatment,65:80:treatment
|
Prior treatment with or intolerance to proteasome inhibitor and immunomodulator
| 1
|
[
"Prior",
"treatment",
"with",
"or",
"intolerance",
"to",
"proteasome",
"inhibitor",
"and",
"immunomodulator"
] |
[
1,
1,
0,
0,
0,
0,
1,
1,
0,
1
] |
NCT02502708
|
34:46:treatment,48:64:treatment,73:82:treatment
|
Patients previously treated with temozolomide, cyclophosphamide, and/or etoposide are eligible for enrollment
| 1
|
[
"Patients",
"previously",
"treated",
"with",
"temozolomide",
",",
"cyclophosphamide",
",",
"and/or",
"etoposide",
"are",
"eligible",
"for",
"enrollment"
] |
[
0,
0,
0,
0,
1,
0,
1,
0,
0,
1,
0,
0,
0,
0
] |
NCT01877382
|
80:88:treatment
|
Confirmation of TP53 nonmutant status is encouraged, but not required prior to DS-3032b dosing
| 1
|
[
"Confirmation",
"of",
"TP53",
"nonmutant",
"status",
"is",
"encouraged",
",",
"but",
"not",
"required",
"prior",
"to",
"DS-3032b",
"dosing"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0
] |
NCT02477839
|
36:59:chronic_disease,61:89:chronic_disease,91:119:chronic_disease,121:136:chronic_disease,141:149:chronic_disease
|
Subject has a current diagnosis of Lennox-Gastaut syndrome, epilepsia partialis continua, primary generalized epilepsy, Dravet Syndorme, or seizures that are not of partial-onset origin
| 1
|
[
"Subject",
"has",
"a",
"current",
"diagnosis",
"of",
"Lennox-Gastaut",
"syndrome",
",",
"epilepsia",
"partialis",
"continua",
",",
"primary",
"generalized",
"epilepsy",
",",
"Dravet",
"Syndorme",
",",
"or",
"seizures",
"that",
"are",
"not",
"of",
"partial-onset",
"origin"
] |
[
0,
0,
0,
0,
0,
0,
2,
2,
0,
2,
2,
2,
0,
2,
2,
2,
0,
2,
2,
0,
0,
2,
0,
0,
0,
0,
0,
0
] |
NCT03033498
|
24:52:chronic_disease,60:69:chronic_disease,71:88:chronic_disease
|
History of significant skin conditions or disorders (e.g., psoriasis, atopic dermatitis, etc.)
| 1
|
[
"History",
"of",
"significant",
"skin",
"conditions",
"or",
"disorders",
"(",
"e.g.",
",",
"psoriasis",
",",
"atopic",
"dermatitis",
",",
"etc",
".",
")"
] |
[
0,
0,
0,
2,
2,
2,
2,
0,
0,
0,
2,
0,
2,
2,
0,
0,
0,
0
] |
NCT02114229
|
73:75:cancer,76:78:cancer,82:85:cancer
|
For Stratum A participants, histologic confirmation of the diagnosis of AT/RT or MRT may be from the original diagnosis or at the time of recurrence/progression
| 1
|
[
"For",
"Stratum",
"A",
"participants",
",",
"histologic",
"confirmation",
"of",
"the",
"diagnosis",
"of",
"AT/RT",
"or",
"MRT",
"may",
"be",
"from",
"the",
"original",
"diagnosis",
"or",
"at",
"the",
"time",
"of",
"recurrence/progression"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01631617
|
1:4:chronic_disease
|
HIV seropositiviy
| 1
|
[
"HIV",
"seropositiviy"
] |
[
2,
0
] |
NCT02615353
|
11:21:chronic_disease
|
Diagnosed depression or other condition that may impact QoL
| 1
|
[
"Diagnosed",
"depression",
"or",
"other",
"condition",
"that",
"may",
"impact",
"QoL"
] |
[
0,
2,
0,
0,
0,
0,
0,
0,
0
] |
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