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NCT00719888
|
,81:93:treatment
|
patients persistently aplastic for greater than one month since completing last chemotherapy are also eligible with PI approval
| 1
|
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NCT02986087
|
1:25:chronic_disease
|
Maternal uterine anomaly
| 1
|
[
"Maternal",
"uterine",
"anomaly"
] |
[
2,
2,
2
] |
NCT02525861
|
37:59:treatment,73:96:treatment,100:122:treatment,116:122:treatment,
|
The participant has participated in another clinical study involving an investigational product or investigational device within 30 days prior to enrollment or is scheduled to participate in another clinical study involving an investigational product or device during the course of this study
| 1
|
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NCT02158793
|
19:37:chronic_disease,51:79:chronic_disease,91:121:chronic_disease
|
Subjects with any cognitive deficits related to a TBI (traumatic brain injury) and or any organic neurological disorders will not be considered for this protocol
| 1
|
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NCT02593123
|
23:26:chronic_disease
|
Negative serology for HIV
| 1
|
[
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"HIV"
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[
0,
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NCT02565446
|
1:32:treatment
|
ventriculoperitoneal (VP) shunt
| 1
|
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1,
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0,
0
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NCT02532621
|
53:88:chronic_disease
|
Subject has a documented and unsuccessfully treated ipsilateral central venous stenosis as determined by imaging
| 1
|
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NCT02169037
|
,71:106:chronic_disease,,,187:198:treatment,202:218:treatment
|
reported incidence of at least two documented episodes of symptomatic paroxysmal atrial fibrillation (AF) during the three months preceding trial entry (at least 1 episode documented by 12-lead ECG or ECG rhythm strip)
| 1
|
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NCT01072370
|
1:39:chronic_disease
|
Severe intrauterine growth restriction
| 1
|
[
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[
2,
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NCT02210650
|
1:12:chronic_disease
|
sarcoidosis
| 1
|
[
"sarcoidosis"
] |
[
2
] |
NCT03033212
|
,42:51:treatment
|
Failed at least 3 months of conservative treatment
| 1
|
[
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NCT02359097
|
66:84:cancer
|
Subjects must have a known or presumed radiological diagnosis of glioblastoma (GBM)
| 1
|
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NCT03183102
|
1:30:chronic_disease,,,,,
|
Chronic hepatobiliary disease, conservatively defined as liver function tests (AST, ALT, alkaline phosphatase, Total Bilirubin) >1.5 times the upper limit of normal
| 1
|
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NCT00432094
|
,165:175:treatment
|
Patients with progressive disease by Response Evaluation Criteria in Solid Tumors (RECIST) criteria by imaging techniques are not eligible to proceed to the second transplant
| 1
|
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NCT01959698
|
8:44:chronic_disease,68:86:chronic_disease,100:120:chronic_disease,154:159:cancer
|
Active central nervous system (CNS) disease defined as symptomatic meningeal lymphoma or known CNS parenchymal lymphoma; a lumbar puncture demonstrating DLBCL at the time of registration to this study is not exclusion for study enrollment
| 1
|
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NCT02309580
|
29:60:treatment,
|
Patients who have undergone autologous stem cell transplant > 6 months prior
| 1
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NCT02460835
|
20:57:allergy_name
|
known allergies to intravenous iodinated contrast agents
| 1
|
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NCT01720147
|
14:16:chronic_disease,27:35:treatment,39:56:treatment
|
Diagnosis of FA proven by DEB test or molecular testing
| 1
|
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NCT02131389
|
44:66:chronic_disease
|
Is a known drug or alcohol abuser or has a psychological disorder that could affect the ability to complete patient reported questionnaires
| 1
|
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NCT02240069
|
125:135:treatment
|
Capable and willing to record symptom data and wood stove usage data, as well as complete pulmonary function testing (i.e., spirometry)
| 1
|
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NCT02725177
|
14:25:chronic_disease
|
Patient with sarcoidosis
| 1
|
[
"Patient",
"with",
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] |
[
0,
0,
2
] |
NCT01993810
|
39:61:cancer,65:70:cancer,89:98:treatment
|
Patients with prior history of either small cell lung cancer or NSCLC regardless of the treatment received
| 1
|
[
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NCT02310399
|
90:111:treatment,
|
Clear surgical reason for poor CI performance that can be remediated with revision CI or contralateral surgery rather than ABI
| 1
|
[
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NCT01384513
|
1:8:cancer,12:43:cancer,49:71:cancer
|
Hodgkin or Indolent Non-Hodgkin's lymphoma with chemosensitive disease
| 1
|
[
"Hodgkin",
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"Indolent",
"Non-Hodgkin",
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"lymphoma",
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[
3,
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NCT02075671
|
,33:55:treatment,46:55:treatment,60:67:chronic_disease,69:82:treatment,84:104:treatment,106:118:treatment,120:132:treatment
|
History of failing at least one conventional treatment for rosacea (metronidazole, sodium sulfacetamide, tetracycline, azelaic acid) or not interested in continuous treatment with these agents
| 1
|
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NCT02591147
|
18:24:chronic_disease
|
is adjacent to a lesion that is either filled or will receive a filling at the time of enrollment
| 1
|
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NCT01261728
|
1:39:treatment
|
Prior radiation therapy to the bladder
| 1
|
[
"Prior",
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"therapy",
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"the",
"bladder"
] |
[
1,
1,
1,
1,
1,
1
] |
NCT01639508
|
1:24:chronic_disease
|
intra-abdominal abscess
| 1
|
[
"intra-abdominal",
"abscess"
] |
[
2,
2
] |
NCT02305537
|
29:38:treatment
|
Patients ineligible for the treatment program
| 1
|
[
"Patients",
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"program"
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[
0,
0,
0,
0,
1,
0
] |
NCT02574728
|
57:67:cancer
|
Participants must have had a histologic verification of malignancy at original diagnosis or relapse
| 1
|
[
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"histologic",
"verification",
"of",
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"at",
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NCT02122081
|
35:44:chronic_disease,46:51:chronic_disease,55:72:chronic_disease,97:106:treatment
|
Patients with active uncontrolled bacterial, viral or fungal infections (undergoing appropriate treatment and with progression of clinical symptoms)
| 1
|
[
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NCT01555554
|
1:20:treatment
|
Sub-arachnoid block (spinal)
| 1
|
[
"Sub-arachnoid",
"block",
"(",
"spinal",
")"
] |
[
1,
1,
0,
0,
0
] |
NCT01622868
|
1:23:cancer
|
Leptomeningeal disease
| 1
|
[
"Leptomeningeal",
"disease"
] |
[
3,
3
] |
NCT02433977
|
9:16:treatment,
|
Current statins use (statins lower ADMA levels), patients may stop and re-enroll after 2 weeks of stopping statins
| 1
|
[
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NCT02570256
|
1:7:chronic_disease
|
STROKE SURVIVORS
| 1
|
[
"STROKE",
"SURVIVORS"
] |
[
2,
0
] |
NCT02429557
|
6:40:chronic_disease,57:82:chronic_disease,84:101:chronic_disease,103:126:chronic_disease,131:153:chronic_disease
|
with neurogenic orthostatic hypotension associated with primary autonomic failure (Parkinson Disease, Multiple System Atrophy and Pure Autonomic Failure)
| 1
|
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NCT02050113
|
12:23:treatment,,,
|
For use of Zenith Flex: diameter >32 mm or <18 mm
| 1
|
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NCT02174549
|
48:51:cancer,88:106:treatment,110:113:treatment,127:132:cancer,,,262:302:cancer,314:334:cancer
|
Patients with single or multiple (2-4 nodules) HCC who are unsuitable or unwilling for surgical resection or RFA. The largest tumor nodule should be less than 10 cm in the largest diameter. The total volume of tumor cannot exceed 50% of liver; or patients with liver metastatic gastrointestinal cancer, including neuroendocrine tumor
| 1
|
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NCT01841333
|
,,,138:147:treatment
|
Serum/urine pregnancy test (for females of childbearing potential) that is negative within 72 hours prior to initiation of first dose of treatment
| 1
|
[
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0,
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0,
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0,
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] |
NCT02365090
|
1:10:chronic_disease,,,,,,
|
Amblyopia with amblyopic eye visual acuity 20/40-20/125, fellow eye visual acuity 20/16-20/25,
| 1
|
[
"Amblyopia",
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[
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
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NCT01525901
|
1:22:chronic_disease
|
hepatic insufficiency
| 1
|
[
"hepatic",
"insufficiency"
] |
[
2,
2
] |
NCT03153319
|
14:25:chronic_disease
|
Diagnosis of MPS I or II
| 1
|
[
"Diagnosis",
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"MPS",
"I",
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"II"
] |
[
0,
0,
2,
2,
2,
2
] |
NCT02437773
|
16:48:chronic_disease,
|
No evidence of suicidal intentions or behaviors in the past 6 months
| 1
|
[
"No",
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"intentions",
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"behaviors",
"in",
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] |
[
0,
0,
0,
2,
2,
2,
2,
0,
0,
0,
0,
0
] |
NCT02496663
|
55:66:treatment,68:86:treatment,143:149:treatment
|
all patients must try to avoid concomitant use of any medications, herbal supplements and/or ingestion of foods with known inducer effects of CYP3A4
| 1
|
[
"all",
"patients",
"must",
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0,
0,
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0,
0,
0,
1
] |
NCT01962415
|
1:36:chronic_disease
|
X-linked adrenoleukodystrophy (ALD)
| 1
|
[
"X-linked",
"adrenoleukodystrophy",
"(",
"ALD",
")"
] |
[
2,
2,
2,
0,
0
] |
NCT02369406
|
1:4:chronic_disease,
|
HIV-negative within 96 hours after birth
| 1
|
[
"HIV-negative",
"within",
"96",
"hours",
"after",
"birth"
] |
[
2,
0,
0,
0,
0,
0
] |
NCT01624090
|
1:20:treatment
|
Thrombolytic agents
| 1
|
[
"Thrombolytic",
"agents"
] |
[
1,
1
] |
NCT02541565
|
69:83:treatment
|
as long as PT or PTT is within therapeutic range of intended use of anticoagulants, or subject is shown to have an antiphospholipid antibody on workup
| 1
|
[
"as",
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"PT",
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"anticoagulants",
",",
"or",
"subject",
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"have",
"an",
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0,
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] |
NCT01884740
|
26:42:cancer
|
radiologically diagnosed brainstem glioma
| 1
|
[
"radiologically",
"diagnosed",
"brainstem",
"glioma"
] |
[
0,
0,
3,
3
] |
NCT03059888
|
35:64:treatment,
|
Subject has undergone a change in immunosuppressive medications within the last three months prior to enrollment
| 1
|
[
"Subject",
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"medications",
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[
0,
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1,
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0,
0,
0,
0,
0,
0,
0
] |
NCT02576444
|
1:24:treatment,
|
Whole blood transfusion in the last 120 days prior to entry to the study
| 1
|
[
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[
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0,
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0,
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0,
0,
0,
0,
0
] |
NCT03035890
|
1:34:chronic_disease
|
primary immunodeficiency syndrome
| 1
|
[
"primary",
"immunodeficiency",
"syndrome"
] |
[
2,
2,
2
] |
NCT01562626
|
,,,82:91:treatment
|
women must have a negative serum or urine pregnancy test 1 week before beginning treatment on this trial
| 1
|
[
"women",
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0,
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0,
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1,
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0
] |
NCT02822378
|
18:38:treatment,
|
systemic oral or transdermal estrogen within the past 3 months
| 1
|
[
"systemic",
"oral",
"or",
"transdermal",
"estrogen",
"within",
"the",
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] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0
] |
NCT02203513
|
,51:77:cancer
|
Patients with gBRCA1/2m with history of or active breast and ovarian cancers are considered for Cohort 1
| 1
|
[
"Patients",
"with",
"gBRCA1/2m",
"with",
"history",
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"or",
"active",
"breast",
"and",
"ovarian",
"cancers",
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[
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3,
3,
3,
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0,
0,
0,
0
] |
NCT03121352
|
46:56:cancer
|
willing to undergo a preliminary biopsy of a metastatic focus for research purposes
| 1
|
[
"willing",
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"a",
"preliminary",
"biopsy",
"of",
"a",
"metastatic",
"focus",
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[
0,
0,
0,
0,
0,
0,
0,
0,
3,
0,
0,
0,
0
] |
NCT02132598
|
,47:59:chronic_disease,
|
Lipase (no radiologic or clinical evidence of pancreatitis) < 2.0 x ULN
| 1
|
[
"Lipase",
"(",
"no",
"radiologic",
"or",
"clinical",
"evidence",
"of",
"pancreatitis",
")",
"<",
"2.0",
"x",
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] |
[
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0
] |
NCT02391987
|
8:26:chronic_disease
|
Active systemic infection
| 1
|
[
"Active",
"systemic",
"infection"
] |
[
0,
2,
2
] |
NCT02354547
|
,43:68:treatment
|
At least 14 days after the last dose of a long-acting growth factor
| 1
|
[
"At",
"least",
"14",
"days",
"after",
"the",
"last",
"dose",
"of",
"a",
"long-acting",
"growth",
"factor"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02748109
|
1:21:chronic_disease,77:107:chronic_disease,109:115:chronic_disease,117:129:chronic_disease,131:157:treatment
|
neurological illness that could potentially explain balance deficits (e.g., Central Nervous System disease, stroke, moderate TBI, lower extremity amputation)
| 1
|
[
"neurological",
"illness",
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"e.g.",
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",",
"stroke",
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[
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2,
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2,
2,
0,
1,
1,
1,
0
] |
NCT01773694
|
,,66:80:treatment
|
will not be returning to the dermatology clinic in 7-14 days for suture removal
| 1
|
[
"will",
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"be",
"returning",
"to",
"the",
"dermatology",
"clinic",
"in",
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02040610
|
1:30:treatment,40:53:treatment,55:66:treatment,71:83:chronic_disease
|
Prior prostate cancer therapy such as: prostatectomy, cryotherapy, or hyperthermia
| 1
|
[
"Prior",
"prostate",
"cancer",
"therapy",
"such",
"as",
":",
"prostatectomy",
",",
"cryotherapy",
",",
"or",
"hyperthermia"
] |
[
1,
1,
1,
1,
0,
0,
0,
1,
0,
1,
0,
0,
2
] |
NCT01582191
|
32:42:allergy_name,44:51:allergy_name,53:68:allergy_name,77:105:allergy_name
|
History of hypersensitivity to vandetanib, lactose, murine products, or any component of the formulation
| 1
|
[
"History",
"of",
"hypersensitivity",
"to",
"vandetanib",
",",
"lactose",
",",
"murine",
"products",
",",
"or",
"any",
"component",
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[
0,
0,
0,
0,
4,
0,
4,
0,
4,
4,
0,
0,
0,
4,
4,
4,
4
] |
NCT01810588
|
1:16:chronic_disease
|
Aplastic anemia
| 1
|
[
"Aplastic",
"anemia"
] |
[
2,
2
] |
NCT02366611
|
13:21:chronic_disease
|
Substantial dementia
| 1
|
[
"Substantial",
"dementia"
] |
[
0,
2
] |
NCT01099644
|
,,83:106:treatment,,
|
Pregnancy testing will be carried out within two weeks prior to administration of radioiodinated Burtomab in females of childbearing age
| 1
|
[
"Pregnancy",
"testing",
"will",
"be",
"carried",
"out",
"within",
"two",
"weeks",
"prior",
"to",
"administration",
"of",
"radioiodinated",
"Burtomab",
"in",
"females",
"of",
"childbearing",
"age"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0
] |
NCT02928991
|
11:49:chronic_disease
|
diagnosed inherited bone marrow failure syndrome
| 1
|
[
"diagnosed",
"inherited",
"bone",
"marrow",
"failure",
"syndrome"
] |
[
0,
2,
2,
2,
2,
2
] |
NCT00001337
|
,,,105:113:cancer
|
greater than 1,000 and platelets greater than 100,000) unless impairment is due to organ involvement by lymphoma or immune-mediated mechanism caused by lymphoma
| 1
|
[
"greater",
"than",
"1,000",
"and",
"platelets",
"greater",
"than",
"100,000",
")",
"unless",
"impairment",
"is",
"due",
"to",
"organ",
"involvement",
"by",
"lymphoma",
"or",
"immune-mediated",
"mechanism",
"caused",
"by",
"lymphoma"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
0,
0,
0,
0,
0,
0
] |
NCT03034213
|
23:46:chronic_disease
|
Suspected presence of enterocutaneous fistula
| 1
|
[
"Suspected",
"presence",
"of",
"enterocutaneous",
"fistula"
] |
[
0,
0,
0,
2,
2
] |
NCT00924027
|
1:21:chronic_disease,33:36:chronic_disease,38:49:chronic_disease
|
autoimmune disorders, including SLE, Scleroderma, etc
| 1
|
[
"autoimmune",
"disorders",
",",
"including",
"SLE",
",",
"Scleroderma",
",",
"etc"
] |
[
2,
2,
0,
0,
2,
0,
2,
0,
0
] |
NCT01624090
|
27:42:chronic_disease,44:67:chronic_disease,82:100:chronic_disease
|
Patients with evidence of active bleeding, intratumoral hemorrhage or history of bleeding diatheses
| 1
|
[
"Patients",
"with",
"evidence",
"of",
"active",
"bleeding",
",",
"intratumoral",
"hemorrhage",
"or",
"history",
"of",
"bleeding",
"diatheses"
] |
[
0,
0,
0,
0,
2,
2,
2,
2,
2,
0,
0,
0,
0,
0
] |
NCT02501096
|
9:43:chronic_disease,48:56:cancer,112:146:treatment,148:158:treatment,163:178:treatment
|
For the non-small cell lung cancer (NSCLC) and melanoma cohorts, participants must have progressed on or after prior treatment with one anti-PD-1, anti-PD-L1, or anti-PDL2 agent
| 1
|
[
"For",
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"lung",
"cancer",
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"and",
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",",
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"with",
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",",
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",",
"or",
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[
0,
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1,
1,
1,
1,
0,
1,
0,
0,
1,
1
] |
NCT02914171
|
156:179:treatment
|
Individuals who have other clinical concerns as documented by a site investigator that could reasonably increase the risk of complications during or after surgical Ebstein repair
| 1
|
[
"Individuals",
"who",
"have",
"other",
"clinical",
"concerns",
"as",
"documented",
"by",
"a",
"site",
"investigator",
"that",
"could",
"reasonably",
"increase",
"the",
"risk",
"of",
"complications",
"during",
"or",
"after",
"surgical",
"Ebstein",
"repair"
] |
[
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
] |
NCT02639208
|
79:91:treatment
|
either in the context of standard treatment or a clinical trial and including chemotherapy
| 1
|
[
"either",
"in",
"the",
"context",
"of",
"standard",
"treatment",
"or",
"a",
"clinical",
"trial",
"and",
"including",
"chemotherapy"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT01983462
|
84:93:treatment
|
Any condition that, in the view of the PI, places the subject at high risk of poor treatment compliance or of not completing the study
| 1
|
[
"Any",
"condition",
"that",
",",
"in",
"the",
"view",
"of",
"the",
"PI",
",",
"places",
"the",
"subject",
"at",
"high",
"risk",
"of",
"poor",
"treatment",
"compliance",
"or",
"of",
"not",
"completing",
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02265315
|
18:54:chronic_disease
|
Individuals with Idiopathic Parkinson's disease (IPD)
| 1
|
[
"Individuals",
"with",
"Idiopathic",
"Parkinson",
"'s",
"disease",
"(",
"IPD",
")"
] |
[
0,
0,
2,
2,
2,
2,
0,
0,
0
] |
NCT03170375
|
6:9:chronic_disease
|
with HTN
| 1
|
[
"with",
"HTN"
] |
[
0,
2
] |
NCT02106650
|
1:25:chronic_disease,,,
|
congestive heart failure Class III/IV according to the New York Heart Association (NYHA) Functional Classification
| 1
|
[
"congestive",
"heart",
"failure",
"Class",
"III/IV",
"according",
"to",
"the",
"New",
"York",
"Heart",
"Association",
"(",
"NYHA",
")",
"Functional",
"Classification"
] |
[
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02871726
|
1:22:treatment
|
Prior prostate biopsy
| 1
|
[
"Prior",
"prostate",
"biopsy"
] |
[
1,
1,
1
] |
NCT02495415
|
,48:76:treatment
|
Diseases refractory/relapsed after one or more systemic cytotoxic therapies
| 1
|
[
"Diseases",
"refractory/relapsed",
"after",
"one",
"or",
"more",
"systemic",
"cytotoxic",
"therapies"
] |
[
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT03121586
|
1:12:treatment
|
Cariprazine
| 1
|
[
"Cariprazine"
] |
[
1
] |
NCT02459119
|
15:25:cancer,49:59:cancer,115:142:cancer
|
Patients with metastatic (lymph node or distant metastasis, i.e. N+ or M1) or locally advanced unresectable (T4b) transitional cell carcinoma
| 1
|
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NCT02390752
|
77:93:chronic_disease,107:131:chronic_disease,133:157:chronic_disease,159:177:chronic_disease,182:219: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
| 1
|
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NCT01989585
|
12:36:chronic_disease,48:69:chronic_disease,74:89:chronic_disease,92:112:treatment,117:125:treatment,,151:164:treatment
|
History of acute coronary syndromes (including myocardial infarction and unstable angina), coronary angioplasty, or stenting within 6 months prior to randomization
| 1
|
[
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NCT02046330
|
31:49:chronic_disease,51:67:chronic_disease,69:82:chronic_disease,87:111:chronic_disease
|
Current or past non-affective psychotic disorder, Bipolar Disorder, Schizophrenia, or Schizoaffective disorder
| 1
|
[
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",",
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"Disorder",
",",
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0,
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2,
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2,
0,
2,
0,
0,
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2
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NCT01174121
|
18:27:treatment
|
The experimental treatment being evaluated in this protocol depends on an intact immune system
| 1
|
[
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"being",
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[
0,
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0,
0,
0,
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NCT02074631
|
31:42:allergy_name
|
Known or suspected allergy to pamidronate or related products
| 1
|
[
"Known",
"or",
"suspected",
"allergy",
"to",
"pamidronate",
"or",
"related",
"products"
] |
[
0,
0,
0,
0,
0,
4,
0,
0,
0
] |
NCT02860000
|
22:47:treatment,51:72:treatment,77:93:cancer,153:156:treatment,
|
Patients who receive stereotactic radiosurgery or whole brain radiation for brain metastases are eligible only if they are asymptomatic and have stable MRI scans for 3 consecutive months, including < 28 days prior to pre-registration
| 1
|
[
"Patients",
"who",
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"or",
"whole",
"brain",
"radiation",
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0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT00230607
|
38:47:treatment
|
be born to a mother who is receiving Fabrazyme during lactation
| 1
|
[
"be",
"born",
"to",
"a",
"mother",
"who",
"is",
"receiving",
"Fabrazyme",
"during",
"lactation"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0
] |
NCT02362997
|
,24:61:treatment,54:61:treatment,62:75:treatment,
|
No more than 1 line of anthracycline-containing chemotherapy prior to ASCT, and no more than 3 lines of therapy total prior to ASCT for arms A and B; no more than 1 line of therapy prior to ASCT for arm C
| 1
|
[
"No",
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"line",
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"chemotherapy",
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0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01676753
|
37:57:chronic_disease
|
Patient has known history of active Hepatitis A, B, or C
| 1
|
[
"Patient",
"has",
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"history",
"of",
"active",
"Hepatitis",
"A",
",",
"B",
",",
"or",
"C"
] |
[
0,
0,
0,
0,
0,
0,
2,
2,
2,
2,
2,
0,
0
] |
NCT02543983
|
1:33:treatment,
|
Treatment with a reversible MAOI within 2 weeks prior to study Phase II
| 1
|
[
"Treatment",
"with",
"a",
"reversible",
"MAOI",
"within",
"2",
"weeks",
"prior",
"to",
"study",
"Phase",
"II"
] |
[
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02317991
|
38:60:treatment,62:74:treatment,76:92:treatment,97:114:treatment,
|
Patients who have received any other investigational agents, chemotherapy, biologic therapy, or radiation therapy within the 28 days prior to Day 1 of the study
| 1
|
[
"Patients",
"who",
"have",
"received",
"any",
"other",
"investigational",
"agents",
",",
"chemotherapy",
",",
"biologic",
"therapy",
",",
"or",
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"therapy",
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"28",
"days",
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02335138
|
52:55:chronic_disease
|
Either partner expresses unwillingness to test for HIV together with his male sexual partner
| 1
|
[
"Either",
"partner",
"expresses",
"unwillingness",
"to",
"test",
"for",
"HIV",
"together",
"with",
"his",
"male",
"sexual",
"partner"
] |
[
0,
0,
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0
] |
NCT02512926
|
32:37:cancer,41:54:cancer,64:69:cancer,85:96:cancer
|
Patients may have asymptomatic CNS 1 or CNS 2 disease, but not CNS 3 or symptomatic CNS disease
| 1
|
[
"Patients",
"may",
"have",
"asymptomatic",
"CNS",
"1",
"or",
"CNS",
"2",
"disease",
",",
"but",
"not",
"CNS",
"3",
"or",
"symptomatic",
"CNS",
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[
0,
0,
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0,
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0,
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0,
0
] |
NCT02047474
|
17:33:chronic_disease,42:62:chronic_disease,73:109:chronic_disease
|
No uncontrolled seizure disorder, active neurological disease, or known central nervous system (CNS) disease
| 1
|
[
"No",
"uncontrolled",
"seizure",
"disorder",
",",
"active",
"neurological",
"disease",
",",
"or",
"known",
"central",
"nervous",
"system",
"(",
"CNS",
")",
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[
0,
0,
2,
2,
0,
0,
2,
2,
0,
0,
0,
2,
2,
2,
2,
2,
0,
0
] |
NCT02423876
|
31:49:treatment
|
Patients must be eligible for epidural placement
| 1
|
[
"Patients",
"must",
"be",
"eligible",
"for",
"epidural",
"placement"
] |
[
0,
0,
0,
0,
0,
1,
1
] |
NCT02739620
|
1:19:cancer,40:46:cancer,58:82:cancer,104:116:treatment
|
metastatic disease, a prior history of cancer, excluding non-melanoma skin cancer, or prior receipt of chemotherapy
| 1
|
[
"metastatic",
"disease",
",",
"a",
"prior",
"history",
"of",
"cancer",
",",
"excluding",
"non-melanoma",
"skin",
"cancer",
",",
"or",
"prior",
"receipt",
"of",
"chemotherapy"
] |
[
3,
3,
0,
0,
0,
0,
0,
3,
0,
0,
3,
3,
3,
0,
0,
0,
0,
0,
1
] |
NCT02864147
|
1:17:chronic_disease,18:24:chronic_disease,35:49:treatment
|
active infection/sepsis requiring IV antibiotics
| 1
|
[
"active",
"infection/sepsis",
"requiring",
"IV",
"antibiotics"
] |
[
2,
2,
0,
1,
1
] |
NCT03170375
|
1:16:chronic_disease
|
hepatic disease
| 1
|
[
"hepatic",
"disease"
] |
[
2,
2
] |
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