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NCT02124902
|
1:11:cancer,15:50:cancer,99:130:cancer
|
basal cell or squamous cell carcinoma of the skin which were treated with local resection only or carcinoma in situ of the cervix
| 3
|
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NCT02340156
|
9:29:chronic_disease
|
Serious nonmalignant disease
| 3
|
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NCT01777035
|
8:29:chronic_disease
|
Severe chronic pain syndrome on admission
| 3
|
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NCT02660528
|
20:39:chronic_disease,46:60:chronic_disease,62:75:chronic_disease,77:92:chronic_disease
|
Recent exposure to uncommon infections (e.g. histoplasmosis, blastomycosis, coccidiomycosis) through recent travel to the Ohio and Mississippi River Valleys and the Southwest
| 3
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NCT02441101
|
35:56:treatment
|
Left ventricular assist device or heart transplantation
| 3
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NCT00719888
|
,,122:153:treatment
|
Diffusion capacity for carbon monoxide corrected (DLCOcorr) > 50% normal or a pediatric patient who is unable to perform pulmonary function tests (PFTs) but has adequate pulmonary function
| 3
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NCT02872857
|
15:32:chronic_disease
|
Presence of a cerebral aneurysm on computed tomographic angiography (CTA) or Angiogram for which clipping or coiling is possible
| 3
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NCT02233868
|
1:17:treatment
|
anticholinergics
| 3
|
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[
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NCT02270450
|
1:18:chronic_disease
|
Bowel obstruction below (distal to) ligament of Treitz
| 3
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NCT02317991
|
1:12:treatment
|
open biopsy
| 3
|
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[
1,
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NCT01880567
|
17:20:cancer
|
Newly Diagnosed MCL: Any serious medical condition that places the patient at unacceptable risk and/or would prevent the subject from signing the informed consent form
| 3
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NCT02266329
|
19:42:chronic_disease,50:65:chronic_disease,67:88:chronic_disease,,106:130:chronic_disease,132:177:chronic_disease,179:203:chronic_disease,,,225:248:chronic_disease,,,
|
Acute or unstable chronic medical illness (e.g., unstable angina, myocardial infarction within 6 months, congestive heart failure, symptomatic or concerning cardiac arrhythmias; pre-existing hypotension (systolic BP<110) or orthostatic hypotension (systolic drop >20 mm mercury (Hg) after 2 min standing accompanied by lightheadedness)
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NCT00539162
|
1:7:cancer,39:51:treatment,55:72:treatment,
|
Cancer-free and have not received any chemotherapy or radiation therapy for >/=12 months prior to enrolling on this study
| 3
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NCT02134392
|
12:38:chronic_disease
|
History of inflammatory bowel disease
| 3
|
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0,
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NCT02402088
|
1:6:chronic_disease,,,
|
Obese BMI group: BMI 30-35 as calculated based on height and weight
| 3
|
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NCT02912572
|
20:60:treatment,52:60:treatment,131:151:treatment,,193:203:treatment
|
Subjects requiring hormone replacement with corticosteroids are eligible if the steroids are administered only for the purpose of hormonal replacement and at doses ≤ 10 mg or 10 mg equivalent prednisone per day
| 3
|
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NCT00967577
|
78:90:cancer,99:114:cancer,159:175:treatment,192:217:treatment
|
Histologically, or cytologically documented, advanced stage, malignant adult solid tumors (except prostate cancer) that are refractory to, or recurrent from, standard therapy or for which no curative standard therapy exists
| 3
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NCT01675154
|
1:37:treatment,9:16:treatment,22:37:treatment,39:46:treatment
|
Current therapy with anti-coagulants, digoxin and anti-arrhythmics
| 3
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NCT02744352
|
1:23:chronic_disease
|
Chronic pain syndromes
| 3
|
[
"Chronic",
"pain",
"syndromes"
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[
2,
2,
2
] |
NCT00358657
|
1:15:chronic_disease
|
Fanconi anemia
| 3
|
[
"Fanconi",
"anemia"
] |
[
2,
2
] |
NCT02213497
|
,,,103:122:treatment,163:165:treatment,169:189:treatment
|
Patients with primary tumors exceeding 8 cm in length or 5 cm in width ( length should be measured by endoscopic findings, width should be measured by diagnostic CT or CT portion of PET/CT)
| 3
|
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NCT02759211
|
33:35:chronic_disease
|
Confirmed clinical diagnosis of MS
| 3
|
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[
0,
0,
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NCT02050347
|
13:22:chronic_disease
|
Mixed donor chimerism (any level)
| 3
|
[
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[
0,
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NCT02762266
|
15:28:chronic_disease,
|
Patients with liver disease classified as Child Pugh class A or B
| 3
|
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NCT02127398
|
1:17:chronic_disease,44:65:chronic_disease,85:106:treatment,108:139:treatment
|
Active infection at other sites (excluding Clostridium difficile) requiring ongoing antibacterial therapy (antiviral or antifungal therapy is acceptable)
| 3
|
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NCT02849639
|
25:36:allergy_name,67:77:allergy_name,81:100:allergy_name,,196:202:treatment
|
No contraindications to Aβ-PET scan including hypersensitivity to PET ligand or radiation exposures in the past year that would exceed the acceptable safe annual exposure in combination with the Aβ PET
| 3
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NCT02520427
|
,,127:137:treatment
|
Women who are lactating/breastfeeding or who plan to breastfeed while on sudy through 1 week after receiving the last dose of study drug
| 3
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NCT02653287
|
110:113:chronic_disease
|
include meeting at least 4 of 11 American College of Rheumatology (ACR) classification criteria for definite SLE, or 3 out of 11 ACR classification criteria with also meeting at least one SLICC criteria
| 3
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NCT01905046
|
23:44:treatment,
|
Administration of any investigational agent =< 30 days prior to pre-registration
| 3
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NCT02390752
|
18:58:cancer
|
Individuals with malignant peripheral nerve sheath tumors will not be eligible to participate in the phase II portion of the trial
| 3
|
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NCT02169089
|
84:100:treatment,102:115:chronic_disease,117:133:treatment
|
Any surgical or medical condition which might alter pharmacokinetics of drug (e.g. renal transplant, liver failure, liver transplant)
| 3
|
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NCT02167958
|
1:30:cancer,34:53:cancer,,99:108:treatment,120:140:treatment,168:189:treatment,219:250:treatment
|
Marginal zone B-cell lymphoma or follicular lymphoma that has progressed after at least two prior therapies (excluding single agent Rituxan) and are ineligible for an autologous transplant or relapsed/progressed after autologous stem cell transplant
| 3
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NCT02589600
|
,20:34:treatment,36:45:treatment,50:70:treatment,,,168:183:treatment
|
Women currently on bisphosphonate, denosumab, or teriparatide therapy or who have been on a bisphosphonate for greater than 1 year during the previous 2 years because bisphosphonates are long acting
| 3
|
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NCT02177695
|
1:26:cancer,28:47:cancer,53:81:cancer
|
pure small cell carcinoma, pure adenocarcinoma, and pure squamous cell carcinoma histologies
| 3
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NCT02822378
|
12:27:chronic_disease
|
history of spinal stenosis
| 3
|
[
"history",
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] |
[
0,
0,
2,
2
] |
NCT02192398
|
13:21:treatment,,,
|
On a stable morphine equivalent dose of at least 60mg/day and ≤ 240mg/day for at least 3 months
| 3
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[
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NCT02548351
|
26:35:chronic_disease
|
Histological presence of cirrhosis
| 3
|
[
"Histological",
"presence",
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"cirrhosis"
] |
[
0,
0,
0,
2
] |
NCT02414139
|
1:26:treatment
|
Strong inducers of CYP3A4
| 3
|
[
"Strong",
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] |
[
1,
1,
1,
1
] |
NCT02574650
|
,,37:52:treatment,
|
Any PCI within 30 days prior to the index procedure or planned 3 months post the index procedure
| 3
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NCT01787487
|
15:27:cancer,59:74:cancer,88:97:treatment
|
patients with malignancies with indolent behavior such as prostate cancer treated with radiation
| 3
|
[
"patients",
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NCT02204098
|
58:66:treatment,75:86:allergy_name,88:93:allergy_name,98:120:allergy_name
|
Known allergy, or history of serious adverse reaction to vaccines such as anaphylaxis, hives, or respiratory difficulty
| 3
|
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NCT01883076
|
,70:92:treatment
|
Child not completing all pre-procedure work-up within 10 days of the Stage II Glenn surgery as listed in section 6 of this protocol AND lack of pre-procedure work-up documented as a safety concern by a site investigator
| 3
|
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NCT02594111
|
1:10:treatment
|
verapamil
| 3
|
[
"verapamil"
] |
[
1
] |
NCT01553071
|
19:36:chronic_disease,,,,
|
Poorly-controlled diabetes mellitus, as defined as fasting serum glucose concentration over 200 mg/dl or a hemoglobin A1C over 7.5%
| 3
|
[
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NCT02016781
|
1:32:cancer,36:51:cancer,52:79:cancer,94:97:cancer
|
Chronic myelomonocytic leukemia or myelodysplastic/myeloproliferative neoplasm (unacceptable MDS subtypes)
| 3
|
[
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"unacceptable",
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0,
0,
3,
0,
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] |
NCT02808442
|
1:30:cancer
|
CD19-negative B-cell leukemia
| 3
|
[
"CD19-negative",
"B-cell",
"leukemia"
] |
[
3,
3,
3
] |
NCT03029442
|
1:40:chronic_disease
|
Acute fracture or extensive bone trauma
| 3
|
[
"Acute",
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"or",
"extensive",
"bone",
"trauma"
] |
[
2,
2,
2,
2,
2,
2
] |
NCT02939755
|
16:32:chronic_disease,34:43:chronic_disease,55:72:chronic_disease
|
no evidence of thought disorder, delusions, or active suicidal ideation is observed or reported
| 3
|
[
"no",
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"delusions",
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0,
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NCT03078504
|
12:28:treatment
|
listed for organ transplant
| 3
|
[
"listed",
"for",
"organ",
"transplant"
] |
[
0,
0,
1,
1
] |
NCT02635360
|
11:26:cancer
|
Confirmed cervical cancer
| 3
|
[
"Confirmed",
"cervical",
"cancer"
] |
[
0,
3,
3
] |
NCT03071328
|
39:69:cancer
|
Histologically confirmed diagnosis of adenocarcinoma of the prostate
| 3
|
[
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"adenocarcinoma",
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"prostate"
] |
[
0,
0,
0,
0,
3,
3,
3,
3
] |
NCT01389024
|
1:37:chronic_disease,46:58:chronic_disease,60:80:chronic_disease,82:103:chronic_disease,136:155:chronic_disease,
|
Upper or lower respiratory infection, active bronchospasm, acute chest syndrome, splenic sequestration or other acute complications of sickle cell disease other than pain in the last 4 weeks (from resolution of symptoms)
| 3
|
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NCT02016924
|
8:41:chronic_disease
|
Active hepatitis C virus (HCV) infection
| 3
|
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0,
2,
2,
2,
2,
2,
0,
0
] |
NCT02978638
|
1:17:chronic_disease
|
Immunosuppressed subjects
| 3
|
[
"Immunosuppressed",
"subjects"
] |
[
2,
0
] |
NCT01430390
|
48:60:cancer,,109:132:treatment,134:143:treatment,145:157:treatment,165:179:treatment
|
Relapse on this protocol is detection of CD19+ malignancies in bone marrow ≥ 5% or extramedullary lesion by morphology cytogenetics, molecular, radiographic and/or flow cytometry
| 3
|
[
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NCT02565498
|
1:19:treatment
|
Prior radiotherapy to the target site
| 3
|
[
"Prior",
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"to",
"the",
"target",
"site"
] |
[
1,
1,
0,
0,
0,
0
] |
NCT02250664
|
1:16:chronic_disease,
|
Suicide attempt in the past 6 months
| 3
|
[
"Suicide",
"attempt",
"in",
"the",
"past",
"6",
"months"
] |
[
2,
2,
0,
0,
0,
0,
0
] |
NCT02106598
|
1:20:chronic_disease,32:59:chronic_disease,64:102:chronic_disease
|
cardiac arrhythmias other than chronic atrial fibrillation and chronic active or persistent hepatitis
| 3
|
[
"cardiac",
"arrhythmias",
"other",
"than",
"chronic",
"atrial",
"fibrillation",
"and",
"chronic",
"active",
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"persistent",
"hepatitis"
] |
[
2,
2,
0,
0,
2,
2,
2,
2,
2,
0,
0,
0,
0
] |
NCT01802346
|
1:39:treatment
|
Prior therapy with inhibitors of IGF-1
| 3
|
[
"Prior",
"therapy",
"with",
"inhibitors",
"of",
"IGF-1"
] |
[
1,
1,
1,
1,
1,
1
] |
NCT02232516
|
1:47:cancer
|
Subcutaneous panniculitis-like T-cell lymphoma
| 3
|
[
"Subcutaneous",
"panniculitis-like",
"T-cell",
"lymphoma"
] |
[
3,
3,
3,
3
] |
NCT02632721
|
46:56:treatment
|
Patients must be eligible for treatment with decitabine
| 3
|
[
"Patients",
"must",
"be",
"eligible",
"for",
"treatment",
"with",
"decitabine"
] |
[
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02579096
|
7:17:treatment
|
Prior febuxostat use
| 3
|
[
"Prior",
"febuxostat",
"use"
] |
[
0,
1,
0
] |
NCT03048448
|
1:28:chronic_disease,,,
|
Moderate hepatic impairment (Group 1): Child-Pugh Class B (7-9 points)
| 3
|
[
"Moderate",
"hepatic",
"impairment",
"(",
"Group",
"1",
")",
":",
"Child-Pugh",
"Class",
"B",
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"7-9",
"points",
")"
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[
2,
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2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02057133
|
13:22:treatment,,25:36:treatment,84:104:treatment,109:127:cancer,157:181:treatment
|
For Part F (LY2835219 + trastuzumab):The participant must have received at least 1 chemotherapy regimen for metastatic disease and may be receiving ongoing therapy with trastuzumab
| 3
|
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NCT02234193
|
23:35:treatment
|
Subjects taking daily oral aspirin
| 3
|
[
"Subjects",
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"oral",
"aspirin"
] |
[
0,
0,
0,
1,
1
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NCT02801539
|
4:30:treatment,
|
On enzyme replacement therapy for ≥ 26 weeks at pretest
| 3
|
[
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"≥",
"26",
"weeks",
"at",
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[
0,
1,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT02128802
|
7:26:treatment
|
Prior anti-reflux surgery
| 3
|
[
"Prior",
"anti-reflux",
"surgery"
] |
[
0,
1,
1
] |
NCT02145351
|
1:28:chronic_disease
|
Hypertrophic cardiomyopathy
| 3
|
[
"Hypertrophic",
"cardiomyopathy"
] |
[
2,
2
] |
NCT02573493
|
45:119:allergy_name
|
History of allergic reactions attributed to compounds of similar chemical or biologic composition to any of the agents used in this study
| 3
|
[
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0,
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0,
0,
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NCT02349867
|
50:67:treatment,94:117:chronic_disease,119:154:chronic_disease,156:181:chronic_disease,183:218:chronic_disease,220:239:chronic_disease,268:286:chronic_disease,298:314:chronic_disease
|
Experienced any of the following toxicities with prior gemcitabine adminstration (if given): capillary leak syndrome, posterior reversible encephalopathy, hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, unexplained dyspnea or other evidence of severe pulmonary toxicity, or severe hepatic toxicity
| 3
|
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NCT02458014
|
15:28:cancer,120:123:cancer,149:161:treatment,,294:311:treatment,313:358:chronic_disease,
|
Patients with B-lineage ALL in hematologic complete remission (CR) with molecular failure (i.e., had never achieved an MRD-negativity status before blinatumomab) or had a molecular relapse (i.e., became MRD positive after having been MRD negative) starting at any time point after 3 months of frontline therapy; molecular disease or minimal residual disease is defined by a value of at least of 1 x 10-4 (0.01%) by multicolor flow cytometry and/or by next generation sequencing (NGS)
| 3
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02281409
|
13:24:treatment,29:35:chronic_disease,55:65:treatment,
|
Subjects on prophylaxis for herpes who started taking medication at least 30 days prior to study entry, should continue to take the prescribed medication for the duration of the study
| 3
|
[
"Subjects",
"on",
"prophylaxis",
"for",
"herpes",
"who",
"started",
"taking",
"medication",
"at",
"least",
"30",
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"prior",
"to",
"study",
"entry",
",",
"should",
"continue",
"to",
"take",
"the",
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"for",
"the",
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0,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00788164
|
1:14:chronic_disease
|
Lichen planus
| 3
|
[
"Lichen",
"planus"
] |
[
2,
2
] |
NCT02573493
|
66:69:chronic_disease,128:135:chronic_disease,139:142:treatment
|
Arm 3: Presence of disease at the oropharynx sub-sites, which is HPV-related as verified by p16, a surrogate marker of HPV, or HPV ISH or PCR
| 3
|
[
"Arm",
"3",
":",
"Presence",
"of",
"disease",
"at",
"the",
"oropharynx",
"sub-sites",
",",
"which",
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"HPV-related",
"as",
"verified",
"by",
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",",
"a",
"surrogate",
"marker",
"of",
"HPV",
",",
"or",
"HPV",
"ISH",
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"PCR"
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[
0,
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02657993
|
113:123:treatment
|
Experiencing ongoing pain and/or stiffness in one or more joints, which started or worsened after initiation of AI therapy
| 3
|
[
"Experiencing",
"ongoing",
"pain",
"and/or",
"stiffness",
"in",
"one",
"or",
"more",
"joints",
",",
"which",
"started",
"or",
"worsened",
"after",
"initiation",
"of",
"AI",
"therapy"
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT03040778
|
15:41:chronic_disease
|
Patients with serious cardiac arrhythmia
| 3
|
[
"Patients",
"with",
"serious",
"cardiac",
"arrhythmia"
] |
[
0,
0,
2,
2,
2
] |
NCT02995733
|
7:11:chronic_disease,48:60:chronic_disease,127:142:chronic_disease,144:169:chronic_disease,188:209:treatment,211:225:chronic_disease,227:234:chronic_disease,240:266:chronic_disease
|
Dx of COPD in a never smoker without any other lung disease or any other disease that might cause airway obstruction such as: Cystic Fibrosis, Connective Tissue Disease, premature birth, organ transplantation, bronchiectasis, sarcoid, and obliterative bronchiolitis
| 3
|
[
"Dx",
"of",
"COPD",
"in",
"a",
"never",
"smoker",
"without",
"any",
"other",
"lung",
"disease",
"or",
"any",
"other",
"disease",
"that",
"might",
"cause",
"airway",
"obstruction",
"such",
"as",
":",
"Cystic",
"Fibrosis",
",",
"Connective",
"Tissue",
"Disease",
",",
"premature",
"birth",
",",
"organ",
"transplantation",
",",
"bronchiectasis",
",",
"sarcoid",
",",
"and",
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"bronchiolitis"
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[
0,
0,
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2,
0,
0,
0,
0,
1,
1,
0,
2,
0,
2,
0,
0,
2,
2
] |
NCT02496208
|
1:36:cancer,38:45:cancer,47:53:cancer,55:67:cancer
|
Urothelial carcinoma of the bladder, urethra, ureter, renal pelvis
| 3
|
[
"Urothelial",
"carcinoma",
"of",
"the",
"bladder",
",",
"urethra",
",",
"ureter",
",",
"renal",
"pelvis"
] |
[
3,
3,
3,
3,
3,
0,
3,
0,
3,
0,
3,
3
] |
NCT02451423
|
1:21:treatment,31:42:treatment,46:60:treatment
|
Inactivated vaccines (such as hepatitis A or polio vaccines) are permitted during the study
| 3
|
[
"Inactivated",
"vaccines",
"(",
"such",
"as",
"hepatitis",
"A",
"or",
"polio",
"vaccines",
")",
"are",
"permitted",
"during",
"the",
"study"
] |
[
1,
1,
0,
0,
0,
1,
1,
0,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT02474199
|
27:30:chronic_disease,34:37:chronic_disease,51:64:treatment
|
No detectible circulating EBV or CMV DNA prior to Treg infusion, assessed at the time of PBMC collection for manufacture
| 3
|
[
"No",
"detectible",
"circulating",
"EBV",
"or",
"CMV",
"DNA",
"prior",
"to",
"Treg",
"infusion",
",",
"assessed",
"at",
"the",
"time",
"of",
"PBMC",
"collection",
"for",
"manufacture"
] |
[
0,
0,
0,
2,
0,
2,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03143985
|
,,109:118:treatment,209:212:treatment,216:224:treatment
|
Men must agree to use a latex or synthetic condom during sexual contact with a FCBP even if they have had a vasectomy from the time of signing the informed consent form through 60 days after the last dose of POM or TEW-7197
| 3
|
[
"Men",
"must",
"agree",
"to",
"use",
"a",
"latex",
"or",
"synthetic",
"condom",
"during",
"sexual",
"contact",
"with",
"a",
"FCBP",
"even",
"if",
"they",
"have",
"had",
"a",
"vasectomy",
"from",
"the",
"time",
"of",
"signing",
"the",
"informed",
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"form",
"through",
"60",
"days",
"after",
"the",
"last",
"dose",
"of",
"POM",
"or",
"TEW-7197"
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[
0,
0,
0,
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1
] |
NCT02287558
|
1:20:chronic_disease,,
|
Renal insufficiency, serum creatinine > 2.0 mg/dl
| 3
|
[
"Renal",
"insufficiency",
",",
"serum",
"creatinine",
">",
"2.0",
"mg/dl"
] |
[
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT02177292
|
1:22:treatment,
|
Prostate tumor biopsy grading by Gleason score classification is mandatory prior to registration (Appendix V)
| 3
|
[
"Prostate",
"tumor",
"biopsy",
"grading",
"by",
"Gleason",
"score",
"classification",
"is",
"mandatory",
"prior",
"to",
"registration",
"(",
"Appendix",
"V",
")"
] |
[
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02498951
|
11:23:treatment,,,
|
high-dose methotrexate is defined as >= 3 grams/m^2; methotrexate dose reduction for creatinine clearance < 100 ml/min is permitted
| 3
|
[
"high-dose",
"methotrexate",
"is",
"defined",
"as",
">",
"=",
"3",
"grams/m^2",
";",
"methotrexate",
"dose",
"reduction",
"for",
"creatinine",
"clearance",
"<",
"100",
"ml/min",
"is",
"permitted"
] |
[
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02133196
|
12:54:allergy_name
|
History of severe immediate hypersensitivity reaction to any of the agents used in this study
| 3
|
[
"History",
"of",
"severe",
"immediate",
"hypersensitivity",
"reaction",
"to",
"any",
"of",
"the",
"agents",
"used",
"in",
"this",
"study"
] |
[
0,
0,
4,
4,
4,
4,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02540616
|
5:25:chronic_disease
|
Any active skin disorder that affects skin integrity of the scalp
| 3
|
[
"Any",
"active",
"skin",
"disorder",
"that",
"affects",
"skin",
"integrity",
"of",
"the",
"scalp"
] |
[
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02188745
|
5:35:treatment,
|
Any investigational cancer therapy in the last 28 days
| 3
|
[
"Any",
"investigational",
"cancer",
"therapy",
"in",
"the",
"last",
"28",
"days"
] |
[
0,
1,
1,
1,
0,
0,
0,
0,
0
] |
NCT02915744
|
14:32:treatment,
|
Last dose of anticancer therapy must have been administered within 6 months of the date of randomization into this study
| 3
|
[
"Last",
"dose",
"of",
"anticancer",
"therapy",
"must",
"have",
"been",
"administered",
"within",
"6",
"months",
"of",
"the",
"date",
"of",
"randomization",
"into",
"this",
"study"
] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00716066
|
1:35:chronic_disease
|
Autoimmune cerebellar degeneration
| 3
|
[
"Autoimmune",
"cerebellar",
"degeneration"
] |
[
2,
2,
2
] |
NCT02233322
|
18:27:treatment,33:42:treatment,47:57:treatment,149:173:chronic_disease
|
May be receiving treatment with phosphate and calcitriol, but must be willing to undergo dose adjustments by the investigators if iron resolves the phosphate wasting defect
| 3
|
[
"May",
"be",
"receiving",
"treatment",
"with",
"phosphate",
"and",
"calcitriol",
",",
"but",
"must",
"be",
"willing",
"to",
"undergo",
"dose",
"adjustments",
"by",
"the",
"investigators",
"if",
"iron",
"resolves",
"the",
"phosphate",
"wasting",
"defect"
] |
[
0,
0,
0,
1,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02385110
|
42:58:chronic_disease,71:81:cancer,100:120:chronic_disease
|
Any serious/and or unstable pre-existing medical disorder (aside from malignancy exception above), psychiatric disorder, or other conditions that could interfere with subject's safety, obtaining informed consent or compliance to the study procedures
| 3
|
[
"Any",
"serious/and",
"or",
"unstable",
"pre-existing",
"medical",
"disorder",
"(",
"aside",
"from",
"malignancy",
"exception",
"above",
")",
",",
"psychiatric",
"disorder",
",",
"or",
"other",
"conditions",
"that",
"could",
"interfere",
"with",
"subject",
"'s",
"safety",
",",
"obtaining",
"informed",
"consent",
"or",
"compliance",
"to",
"the",
"study",
"procedures"
] |
[
0,
0,
0,
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2,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01953263
|
44:66:chronic_disease,70:90:chronic_disease,102:138:treatment
|
Patients with evidence or diagnosis of any primary muscle disease or coagulation disorder (including concomitant anti-coagulation therapy)
| 3
|
[
"Patients",
"with",
"evidence",
"or",
"diagnosis",
"of",
"any",
"primary",
"muscle",
"disease",
"or",
"coagulation",
"disorder",
"(",
"including",
"concomitant",
"anti-coagulation",
"therapy",
")"
] |
[
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
0,
2,
2,
0,
0,
1,
1,
1,
0
] |
NCT01937949
|
1:11:chronic_disease,13:23:chronic_disease,27:67:chronic_disease,
|
Juxtarenal, suprarenal or type IV thoracoabdominal aortic aneurysm with a diameter ≥ 5.0 cm or 2 times the normal aortic diameter
| 3
|
[
"Juxtarenal",
",",
"suprarenal",
"or",
"type",
"IV",
"thoracoabdominal",
"aortic",
"aneurysm",
"with",
"a",
"diameter",
"≥",
"5.0",
"cm",
"or",
"2",
"times",
"the",
"normal",
"aortic",
"diameter"
] |
[
2,
0,
2,
0,
2,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00875342
|
8:17:treatment
|
Use of pacemaker
| 3
|
[
"Use",
"of",
"pacemaker"
] |
[
0,
0,
1
] |
NCT01554371
|
,,,152:168:treatment,
|
Female patient of childbearing potential must have a negative serum or urine pregnancy test β-hCG within 72 hours prior to receiving the first dose of study medication and agree to the use of effective methods of contraception while on study
| 3
|
[
"Female",
"patient",
"of",
"childbearing",
"potential",
"must",
"have",
"a",
"negative",
"serum",
"or",
"urine",
"pregnancy",
"test",
"β-hCG",
"within",
"72",
"hours",
"prior",
"to",
"receiving",
"the",
"first",
"dose",
"of",
"study",
"medication",
"and",
"agree",
"to",
"the",
"use",
"of",
"effective",
"methods",
"of",
"contraception",
"while",
"on",
"study"
] |
[
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,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02094625
|
1:10:treatment,
|
Cisplatin must be delivered over <3 day
| 3
|
[
"Cisplatin",
"must",
"be",
"delivered",
"over",
"<",
"3",
"day"
] |
[
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02435992
|
,49:66:chronic_disease,68:83:chronic_disease,88:105:chronic_disease
|
Current or recent (within 3 months) evidence of fulminant colitis, toxic megacolon, or bowel perforation
| 3
|
[
"Current",
"or",
"recent",
"(",
"within",
"3",
"months",
")",
"evidence",
"of",
"fulminant",
"colitis",
",",
"toxic",
"megacolon",
",",
"or",
"bowel",
"perforation"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
2,
2,
0,
0,
2,
2
] |
NCT01896999
|
29:59:cancer
|
other histologies including lymphocyte predominant (LP) HL are not permitted
| 3
|
[
"other",
"histologies",
"including",
"lymphocyte",
"predominant",
"(",
"LP",
")",
"HL",
"are",
"not",
"permitted"
] |
[
0,
0,
0,
3,
3,
3,
3,
0,
0,
0,
0,
0
] |
NCT02151175
|
15:23:chronic_disease,25:33:chronic_disease,38:47:chronic_disease
|
Subjects with dementia, delirium and psychotic symptoms
| 3
|
[
"Subjects",
"with",
"dementia",
",",
"delirium",
"and",
"psychotic",
"symptoms"
] |
[
0,
0,
2,
0,
2,
0,
2,
0
] |
NCT02355535
|
1:26:treatment,31:49:cancer,98:116:treatment,118:145:treatment,147:159:treatment,161:177:treatment,182:205:treatment
|
Prior systemic treatments for metastatic disease are permitted but may not be ongoing, including targeted therapies, biologic response modifiers, chemotherapy, hormonal therapy, or investigational therapy
| 3
|
[
"Prior",
"systemic",
"treatments",
"for",
"metastatic",
"disease",
"are",
"permitted",
"but",
"may",
"not",
"be",
"ongoing",
",",
"including",
"targeted",
"therapies",
",",
"biologic",
"response",
"modifiers",
",",
"chemotherapy",
",",
"hormonal",
"therapy",
",",
"or",
"investigational",
"therapy"
] |
[
1,
1,
1,
0,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
1,
1,
1,
0,
1,
0,
1,
1,
0,
0,
1,
1
] |
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