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NCT02682407
|
1:12:chronic_disease
|
hepatitis B
| 1
|
[
"hepatitis",
"B"
] |
[
2,
2
] |
NCT02803359
|
12:30:chronic_disease
|
History of Neurologic Disease
| 1
|
[
"History",
"of",
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"Disease"
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[
0,
0,
2,
2
] |
NCT02508038
|
10:14:chronic_disease,26:30:chronic_disease,42:45:chronic_disease
|
MPX for: HepB (HBV-PCR), HepC (HCV-PCR), HIV (HIV-PCR)
| 1
|
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NCT02905370
|
1:25:chronic_disease
|
Congestive Heart Failure
| 1
|
[
"Congestive",
"Heart",
"Failure"
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[
2,
2,
2
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NCT02530034
|
1:49:cancer
|
chronic myeloid leukemia in blast phase (CML-BP)
| 1
|
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NCT02097121
|
27:35:treatment
|
Current use of indwelling catheter or clean intermittent catheterization to empty the bladder
| 1
|
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NCT03169543
|
1:32:chronic_disease
|
debilitating medical conditions
| 1
|
[
"debilitating",
"medical",
"conditions"
] |
[
2,
2,
2
] |
NCT02584647
|
42:52:cancer,
|
Subjects with a completely treated prior malignancy and no evidence of disease for ≥ 2 years are eligible
| 1
|
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NCT01829958
|
26:31:cancer
|
Previously untreated for DLBCL
| 1
|
[
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[
0,
0,
0,
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NCT01581580
|
42:61:chronic_disease,71:90:chronic_disease,94:98:chronic_disease
|
current or pre-existing life-threatening respiratory disease, such as respiratory failure or ARDS
| 1
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NCT00734877
|
,,37:44:cancer
|
Platelet count < 30 x 109/L, unless myeloma-related
| 1
|
[
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NCT02577406
|
,,,,,389:398:treatment,436:446:treatment,484:495:treatment
|
Male subjects must agree to practice true abstinence from sexual intercourse or to the use of highly effective contraceptive methods (as described above) with non-pregnant female partners of childbearing potential at screening and throughout the course of the study, and should avoid conception with their partners during the course of the study and for 4 months following the last study treatment (6 months following the last dose of cytarabine; 6 months following the last dose of azacitidine in Canada)
| 1
|
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NCT02352480
|
5:15:cancer
|
any malignancy in the wound area
| 1
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"area"
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[
0,
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0,
0,
0,
0
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NCT02402660
|
1:9:chronic_disease
|
glaucoma
| 1
|
[
"glaucoma"
] |
[
2
] |
NCT02724540
|
1:17:chronic_disease,31:40:chronic_disease,45:61:chronic_disease
|
Active infection (Symptomatic bacterial and fungal infection - newly diagnosed and/or requiring treatment)
| 1
|
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NCT01976429
|
10:28:chronic_disease
|
existing middle-ear disease
| 1
|
[
"existing",
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"disease"
] |
[
0,
2,
2
] |
NCT01972113
|
28:31:allergy_name
|
Subjects with a history of soy allergy
| 1
|
[
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0,
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0
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NCT03186937
|
10:23:chronic_disease
|
Operable breast cancer
| 1
|
[
"Operable",
"breast",
"cancer"
] |
[
0,
2,
2
] |
NCT01430390
|
1:11:chronic_disease
|
Cytopenias deemed to be disease-related and not therapy-related
| 1
|
[
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"be",
"disease-related",
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] |
[
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT03008070
|
1:22:chronic_disease
|
Diabetic ketoacidosis
| 1
|
[
"Diabetic",
"ketoacidosis"
] |
[
2,
2
] |
NCT02776891
|
12:20:cancer
|
Double hit lymphoma
| 1
|
[
"Double",
"hit",
"lymphoma"
] |
[
0,
0,
3
] |
NCT02208362
|
126:135:treatment
|
Research participants with any non-malignant intercurrent illness which is either poorly controlled with currently available treatment, or which is of such severity that the investigators deem it unwise to enter the research participant on protocol
| 1
|
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NCT02323126
|
53:71:chronic_disease
|
any known or suspected, current or past history of, autoimmune disease
| 1
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NCT02234193
|
24:32:treatment,76:90:treatment,110:116:treatment
|
Willingness to undergo biopsies of full-thickness skin tissue from the pre-abdominoplasty skin, and have the biopsy sites marked by tattoos
| 1
|
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NCT01851694
|
1:24:chronic_disease
|
Abnormal renal function
| 1
|
[
"Abnormal",
"renal",
"function"
] |
[
2,
2,
2
] |
NCT02112617
|
83:100:treatment
|
Participants or their legal guardian must sign consent prior to the initiation of radiation therapy
| 1
|
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NCT02427841
|
,,,,156:168:treatment,,,
|
Women of child-bearing potential and men must be willing to use adequate contraception during the entire study and for 8 weeks following completion of all chemotherapy on study; this includes hormonal or barrier method, or abstinence
| 1
|
[
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NCT02418195
|
1:21:chronic_disease
|
Polyarteritis nodosa
| 1
|
[
"Polyarteritis",
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] |
[
2,
2
] |
NCT02952534
|
29:64:chronic_disease
|
molecular evidence of other homologous recombination deficiency
| 1
|
[
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[
0,
0,
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0,
2,
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] |
NCT03037931
|
8:21:chronic_disease,,,,38:76:treatment,,158:171:treatment
|
Stable heart failure (NYHA II-IV) on maximally-tolerated background therapy (as determined by the site Principle Investigator) for at least 2 weeks prior to randomization
| 1
|
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NCT02394028
|
1:49:treatment,54:56:chronic_disease,86:95:chronic_disease
|
Treatment with antibiotics as adjunctive therapy for CD in the absence of documented infection
| 1
|
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NCT02875301
|
1:12:chronic_disease
|
Parkinson's
| 1
|
[
"Parkinson",
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] |
[
2,
2
] |
NCT01970176
|
17:34:treatment,38:68:treatment,70:82:treatment,84:96:treatment,98:110:treatment,112:122:treatment,124:134:treatment,138:164:treatment,169:172:chronic_disease,204:215:treatment
|
Patients taking alpha antagonists or cytochrome P450 3A4 inhibitors (ketoconazole, itraconazole, erythromycin, saquinavir, cimetidine or serum proteases inhibitors for HIV) who cannot be taken off these medications for the duration of the study
| 1
|
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NCT02418195
|
23:41:chronic_disease
|
A lifetime history of psychotic disorder
| 1
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NCT02519322
|
42:60:chronic_disease
|
Subjects with active, known or suspected autoimmune disease
| 1
|
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NCT02407171
|
,,131:141:treatment
|
childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication
| 1
|
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NCT02723266
|
23:31:chronic_disease
|
signs and symptoms of diabetes
| 1
|
[
"signs",
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[
0,
0,
0,
0,
2
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NCT02332369
|
1:13:chronic_disease
|
Iris atrophy
| 1
|
[
"Iris",
"atrophy"
] |
[
2,
2
] |
NCT02172651
|
16:25:treatment,29:46:treatment,87:103:cancer
|
Prior systemic treatment or radiation therapy is allowed for patients with resectable liver metastases
| 1
|
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NCT02061761
|
79:84:cancer
|
For dose escalation and dose expansion in combination with BMS-936558: HL and DLBCL
| 1
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NCT02474173
|
21:37:cancer,145:179:chronic_disease,378:386:treatment,398:415:treatment,,487:495:chronic_disease
|
Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events; however, patients with previously treated and stable brain metastases are eligible as long as they are no longer requiring steroids, completed radiation therapy more than 2 weeks prior to the first dose of study regimen and have no seizures or worsening neurologic symptoms
| 1
|
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NCT02349867
|
,,,100:109:treatment
|
Any other hemorrhage/bleeding event >= grade 3 (CTCAE v4.0) within 12 weeks prior to initiation of treatment
| 1
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NCT02235623
|
1:25:chronic_disease
|
Bilateral cryptorchidism
| 1
|
[
"Bilateral",
"cryptorchidism"
] |
[
2,
2
] |
NCT03014687
|
54:77:chronic_disease
|
Concurrent antibiotics for another indication (i.e., urinary tract infection)
| 1
|
[
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"i.e.",
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0,
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NCT02913430
|
1:29:cancer
|
skin squamous cell carcinoma
| 1
|
[
"skin",
"squamous",
"cell",
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] |
[
3,
3,
3,
3
] |
NCT01776190
|
49:58:treatment,
|
You are unable to come in three days a week for treatment for a 10-week period
| 1
|
[
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NCT02037048
|
24:66:treatment,73:129:treatment,130:159:treatment,177:187:treatment,188:194:treatment
|
staging should include upper endoscopy with endoscopic ultrasound and a fludeoxyglucose (FDG)-positron emission tomography (PET)/computed tomography (CT) scan (with diagnostic CT abdomen/pelvis preferred)
| 1
|
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NCT02056873
|
13:22:chronic_disease
|
Presence of psychotic features
| 1
|
[
"Presence",
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[
0,
0,
2,
0
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NCT02213913
|
7:10:chronic_disease
|
Known HIV positive status
| 1
|
[
"Known",
"HIV",
"positive",
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] |
[
0,
2,
0,
0
] |
NCT02495168
|
23:47:treatment
|
Patients who required systemic corticosteroids (for any reason)
| 1
|
[
"Patients",
"who",
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"systemic",
"corticosteroids",
"(",
"for",
"any",
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")"
] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
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NCT02200445
|
10:17:chronic_disease
|
Abnormal thyroid function tests
| 1
|
[
"Abnormal",
"thyroid",
"function",
"tests"
] |
[
0,
2,
0,
0
] |
NCT02003222
|
21:55:chronic_disease
|
Patients with known human immunodeficiency virus (HIV) infection
| 1
|
[
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"known",
"human",
"immunodeficiency",
"virus",
"(",
"HIV",
")",
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[
0,
0,
0,
2,
2,
2,
2,
0,
0,
0
] |
NCT03125226
|
4:20:treatment
|
No prior cystectomy
| 1
|
[
"No",
"prior",
"cystectomy"
] |
[
0,
1,
1
] |
NCT01389024
|
23:41:chronic_disease,43:56:chronic_disease,61:96:chronic_disease,98:113:chronic_disease,,
|
Participant must have sickle cell anemia (hemoglobin SS) or sickle Beta-zero (null) thalassemia (hemoglobin S-B0) as confirmed at the local institution by hemoglobin analysis after six months of age
| 1
|
[
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NCT00924027
|
1:21:cancer,64:76:treatment
|
gynecological cancer patients who may have received concurrent chemotherapy as a component of their treatment regimen
| 1
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NCT00492778
|
34:55:cancer
|
Patients with a history of other invasive malignancies
| 1
|
[
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[
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NCT03034863
|
27:36:chronic_disease
|
untreated or un-medicated psychosis
| 1
|
[
"untreated",
"or",
"un-medicated",
"psychosis"
] |
[
0,
0,
0,
2
] |
NCT00716066
|
1:18:chronic_disease
|
Myasthenia Gravis
| 1
|
[
"Myasthenia",
"Gravis"
] |
[
2,
2
] |
NCT01631617
|
28:33:allergy_name,35:46:allergy_name,51:75:allergy_name,80:89:allergy_name,93:104:allergy_name
|
Known allergic reaction to sulfa, beta-lactam, or tetracycline class drugs; or lidocaine or epinephrine
| 1
|
[
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",",
"beta-lactam",
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"tetracycline",
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"lidocaine",
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4,
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4,
0,
0,
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4,
4,
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0,
4,
0,
4
] |
NCT02098876
|
13:32:chronic_disease,50:65:chronic_disease,59:65:chronic_disease,90:105:chronic_disease
|
Evidence of myocardial ischemia (e.g., stable or unstable angina, post-infarct angina or silent ischemia) suitable for PCI
| 1
|
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0,
0
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NCT02393794
|
1:14:cancer,30:47:chronic_disease,64:80:treatment
|
Breast cancer that is either stage III disease not amenable to curative therapy or stage IV
| 1
|
[
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NCT01371630
|
15:38:cancer,
|
Patients with refractory-relapsed ALL of any age are eligible
| 1
|
[
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"ALL",
"of",
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[
0,
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3,
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0,
0,
0,
0,
0
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NCT02520791
|
,88:124:treatment,126:163:treatment,203:207:cancer,209:213:cancer,218:237:cancer,326:335:cancer,337:341:cancer,346:348:cancer
|
Patients must have at least one measurable lesion that can be accurately measured with spiral computed tomography (CT) scan, magnetic resonance imaging (MRI) scan, or physical exam (by calipers only); (PTCL, AITL and follicular lymphoma patients will be assessed on this study using the Lugano criteria for the evaluation of lymphomas; CTCL and MF patients will be assessed using International Society for Cutaneous Lymphomas [ISCL] and European Organization for Research and Treatment of Cancer [EORTC criteria])
| 1
|
[
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NCT02378714
|
27:56:chronic_disease
|
medications indicated for bipolar or psychotic disorder if prescribed for bipolar or psychotic disorder
| 1
|
[
"medications",
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NCT00819208
|
63:75:treatment
|
patients who are pre-planned to receive a shorter duration of chemotherapy, including as part of a research study
| 1
|
[
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0,
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0,
0,
0,
0
] |
NCT00734877
|
,,46:69:cancer
|
Zubrod ≤ 2, unless solely due to symptoms of MM-related bone disease
| 1
|
[
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",",
"unless",
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"due",
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"bone",
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[
0,
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3
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NCT01712308
|
20:58:chronic_disease,63:79:chronic_disease,85:102:chronic_disease
|
Known positive for human immunodeficiency virus-1 (HIV-1), or active infection with hepatitis-B or -C
| 1
|
[
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"for",
"human",
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"virus-1",
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",",
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[
0,
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2,
2,
2,
0,
0,
0,
0,
2,
2,
0,
2,
2,
2
] |
NCT00488696
|
1:27:chronic_disease
|
Uncorrectable coagulopathy
| 1
|
[
"Uncorrectable",
"coagulopathy"
] |
[
2,
2
] |
NCT02460783
|
,,56:67:treatment
|
weight less than or equal to 350 lbs (weight limit for MRI scanner)
| 1
|
[
"weight",
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"350",
"lbs",
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"weight",
"limit",
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"MRI",
"scanner",
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[
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0
] |
NCT02477839
|
16:42:chronic_disease
|
Subject has an arrhythmic heart condition requiring medical therapy
| 1
|
[
"Subject",
"has",
"an",
"arrhythmic",
"heart",
"condition",
"requiring",
"medical",
"therapy"
] |
[
0,
0,
0,
2,
2,
2,
0,
0,
0
] |
NCT02600754
|
10:18:chronic_disease
|
probable dementia
| 1
|
[
"probable",
"dementia"
] |
[
0,
2
] |
NCT03100461
|
1:22:chronic_disease
|
Acute medical illness
| 1
|
[
"Acute",
"medical",
"illness"
] |
[
2,
2,
2
] |
NCT02457845
|
1:22:treatment,
|
Monoclonal antibodies: At least 3 half-lives must have elapsed prior to study entry
| 1
|
[
"Monoclonal",
"antibodies",
":",
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"half-lives",
"must",
"have",
"elapsed",
"prior",
"to",
"study",
"entry"
] |
[
1,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00358657
|
4:42:treatment,46:75:treatment,89:112:chronic_disease,123:138:chronic_disease,149:156:treatment,197:212:chronic_disease
|
on multiple-gated acquisition (MUGA) scan or cardiac echocardiogram (echo), symptomatic coronary artery disease, or other cardiac failure requiring therapy; patients with a history of, or current cardiac disease should be evaluated with appropriate cardiac studies and/or cardiology consult
| 1
|
[
"on",
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NCT02398240
|
,,36:39:treatment
|
Females who are pregnant (positive HCG)
| 1
|
[
"Females",
"who",
"are",
"pregnant",
"(",
"positive",
"HCG",
")"
] |
[
0,
0,
0,
0,
0,
0,
1,
0
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NCT02346526
|
7:17:cancer,
|
Other malignancy treated within the last 3 years
| 1
|
[
"Other",
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"within",
"the",
"last",
"3",
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] |
[
0,
3,
0,
0,
0,
0,
0,
0
] |
NCT01950234
|
1:5:chronic_disease,7:11:chronic_disease,16:20:chronic_disease
|
SPMS, PPMS, or PRMS phenotype, according to Lublin and Reingold criteria
| 1
|
[
"SPMS",
",",
"PPMS",
",",
"or",
"PRMS",
"phenotype",
",",
"according",
"to",
"Lublin",
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"Reingold",
"criteria"
] |
[
2,
0,
2,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02425566
|
19:34:chronic_disease
|
Subjects with any chronic disease
| 1
|
[
"Subjects",
"with",
"any",
"chronic",
"disease"
] |
[
0,
0,
0,
2,
2
] |
NCT02390752
|
22:24:chronic_disease,73:77:cancer,82:94:cancer,146:154:cancer,158:179:cancer,289:304:cancer,321:338:chronic_disease,376:392:chronic_disease,451:454:chronic_disease
|
Phase II: inoperable PN causing morbidity, such as (but not limited to) head and neck lesions that could compromise the airway or great vessels, brachial or lumbar plexus lesions that could cause nerve compression and loss of function, lesions that could result in major deformity (e.g., orbital lesions) or significant cosmetic problems, lesions of the extremity that cause limb hypertrophy or loss of function, and painful lesions in patients with NF1
| 1
|
[
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NCT02162420
|
1:23:chronic_disease
|
Uncontrolled infection
| 1
|
[
"Uncontrolled",
"infection"
] |
[
2,
2
] |
NCT02905188
|
11:47:treatment
|
Available autologous transduced T cell product
| 1
|
[
"Available",
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"cell",
"product"
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[
0,
1,
1,
1,
1,
1
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NCT02417701
|
13:37:chronic_disease
|
symptomatic congestive heart failure
| 1
|
[
"symptomatic",
"congestive",
"heart",
"failure"
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[
0,
2,
2,
2
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NCT02563678
|
51:73:chronic_disease,75:102:chronic_disease,104:111:chronic_disease,115:161:chronic_disease,163:181:chronic_disease,183:206:chronic_disease,208:235:chronic_disease,237:243:chronic_disease,245:251:chronic_disease,253:269:chronic_disease,273:286:chronic_disease,288:307:chronic_disease,309:326:chronic_disease,331:345:chronic_disease,346:361:chronic_disease
|
History of significant health problems, including metabolic bone disease, skeletal muscle pathologies, cardiac or peripheral cardiovascular system abnormalities, clotting disorders, coronary artery disease, peripheral vascular disease, stroke, cancer, high cholesterol or triglycerides, high blood pressure, diabetes mellitus, or impaired liver/kidney function
| 1
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NCT02358681
|
31:40:treatment
|
Contraindication to receiving ketorolac
| 1
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NCT01238120
|
20:29:allergy_name
|
Have an allergy to ibuprofen
| 1
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[
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0,
0,
0,
4
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NCT01461837
|
23:27:treatment
|
Previously received a HSCT
| 1
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[
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[
0,
0,
0,
1
] |
NCT03087903
|
1:14:treatment,16:25:treatment,30:75:treatment,,94:109:treatment
|
Major surgery, radiation, or treatment with any other investigational drug within 2 weeks of study treatment
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NCT02111850
|
,50:72:treatment,110:129:treatment,,228:236:chronic_disease,240:248:chronic_disease
|
More than four weeks must have elapsed since any prior systemic therapy at the time the patient receives the preparative regimen, and patients' toxicities must have recovered to a grade 1 or less (except for toxicities such as alopecia or vitiligo)
| 1
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NCT01681589
|
39:64:chronic_disease,66:99:chronic_disease,114:134:chronic_disease,143:154:chronic_disease,162:168:chronic_disease,170:178:chronic_disease,182:203:chronic_disease
|
Complicating medical problems such as uncontrolled hypertension, diabetes with signs of neuropathy, and previous neurological illness such as head trauma, prior stroke, epilepsy or demyelinating disease, implanted neuromodulatory or electronic device, metal in head
| 1
|
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NCT02841540
|
19:52:chronic_disease,54:86:chronic_disease,88:119:chronic_disease,121:142:chronic_disease,163:184:chronic_disease
|
Family history of Leber Hereditary Optic Neuropathy, Autosomal Dominant Optic Atrophy, Late-Onset Retinal Degeneration, Familial Dysautonomia or other hereditary mitochondrial disease, unless the causative mutation(s) in the family have been determined and the participant has tested negative for the mutation(s)
| 1
|
[
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NCT02411656
|
24:58:chronic_disease
|
Has a known history of human immunodeficiency virus (HIV)
| 1
|
[
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2,
2,
2,
0,
0
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NCT03104699
|
40:50:cancer,71:83:cancer,97:113:treatment
|
Histologically or cytologically proven metastatic or locally advanced solid tumors for which no standard therapy exists or standard therapy has failed
| 1
|
[
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"cytologically",
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"solid",
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0,
0
] |
NCT01681264
|
16:25:treatment,16:33:treatment,77:86:treatment,90:103:treatment,110:118:treatment,120:127:treatment,188:192:chronic_disease
|
Currently in a treatment program for alcohol or drug abuse, or currently on methadone or buprenorphine (i.e. suboxone, subutex) for treatment of addiction, or stimulants for treatment of ADHD
| 1
|
[
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NCT03181893
|
19:41:chronic_disease,50:68:chronic_disease,86:107:chronic_disease
|
Have pre existing demyelinating disorder such as multiple sclerosis, or other severe neurological deficits
| 1
|
[
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0,
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2,
0,
0,
0,
0,
2,
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NCT03101085
|
16:22:cancer,39:51:treatment,55:72:treatment,
|
any history of cancer that required a chemotherapy or radiation therapy intervention within the past 5 years
| 1
|
[
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0,
0,
0,
0,
0
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NCT03154580
|
1:22:chronic_disease,29:35:chronic_disease,37:45:chronic_disease
|
Neurological diseases (e.g. stroke, seizures)
| 1
|
[
"Neurological",
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"e.g",
".",
"stroke",
",",
"seizures",
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[
2,
2,
0,
0,
0,
2,
0,
2,
0
] |
NCT02479906
|
39:61:treatment,
|
Subject is currently participating in another clinical study or enrolled in another clinical study within 30 days prior to this study
| 1
|
[
"Subject",
"is",
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"in",
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0,
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0,
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0,
0,
0
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NCT02414139
|
29:32:cancer
|
Patients with characterized ALK-positive rearrangement
| 1
|
[
"Patients",
"with",
"characterized",
"ALK-positive",
"rearrangement"
] |
[
0,
0,
0,
3,
0
] |
NCT02355535
|
18:29:chronic_disease,31:49:chronic_disease,54:57:chronic_disease,79:102:treatment
|
Has a history of blood clots, pulmonary embolism, or DVT unless controlled by anticoagulant treatment
| 1
|
[
"Has",
"a",
"history",
"of",
"blood",
"clots",
",",
"pulmonary",
"embolism",
",",
"or",
"DVT",
"unless",
"controlled",
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"treatment"
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[
0,
0,
0,
0,
2,
2,
0,
2,
2,
0,
0,
2,
0,
0,
0,
1,
1
] |
NCT02796209
|
1:24:chronic_disease
|
Impaired renal function
| 1
|
[
"Impaired",
"renal",
"function"
] |
[
2,
2,
2
] |
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