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NCT02991144
|
19:44:treatment,
|
On stable dose of ammonia scavenger therapy for ≥4 weeks
| 1
|
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NCT02401074
|
1:16:chronic_disease,
|
Unstable asthma as indicated by self report of increased symptoms or increased beta-agonist use over the 2 weeks preceding the screening visit
| 1
|
[
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NCT02520778
|
23:46:treatment
|
be treatment naive to T790M-directed EGFR TKI
| 1
|
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NCT02227199
|
14:24:chronic_disease
|
uncontrolled arrhythmia
| 1
|
[
"uncontrolled",
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] |
[
0,
2
] |
NCT02342782
|
13:56:treatment,100:125:treatment,192:215:treatment,,,
|
Significant prior external beam dose-limiting radiation to a critical organ based on review of the prior radiation treatment records by the Radiation Oncology PI; patients who have had prior external beam radiation > 2000 cGy (at 180 to 200 cGy per day) to the lung will be ineligible
| 1
|
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NCT02444689
|
18:46:treatment
|
New / changes in anti-hypertensive medication
| 1
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NCT02561988
|
1:7:cancer
|
SM-AHN
| 1
|
[
"SM-AHN"
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[
3
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NCT01333046
|
31:40:treatment
|
multiply relapsed patients in remission who are at a high risk of relapse
| 1
|
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NCT02406885
|
13:27:treatment
|
Inducers of p-glycoprotein
| 1
|
[
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[
0,
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NCT02411773
|
1:20:chronic_disease
|
Diabetic Neuropathy
| 1
|
[
"Diabetic",
"Neuropathy"
] |
[
2,
2
] |
NCT02163317
|
1:35:chronic_disease
|
human immunodeficiency virus (HIV) testing
| 1
|
[
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[
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NCT03171493
|
31:41:cancer
|
Patients with any other prior malignancy are not allowed
| 1
|
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NCT02932280
|
52:65:treatment,
|
have recovered from the acute toxic effects of all prior therapy to ≤ grade 1 before entering this study
| 1
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NCT02418195
|
1:4:chronic_disease,26:41:chronic_disease,48:65:chronic_disease
|
MDD Participants without Suicide Attempt, with Suicidal Ideation
| 1
|
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NCT02565498
|
7:17:cancer,
|
Prior malignancy within the previous five years
| 1
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NCT01631617
|
28:55:allergy_name
|
Known allergic reaction to sodium hypochlorite (NaOCl)
| 1
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NCT01873131
|
46:55:treatment
|
Willingness of parent/guardian to follow the treatment schedule and post treatment care requirements
| 1
|
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NCT02481310
|
6:28:cancer
|
MYC+ plasmablastic lymphoma by histology
| 1
|
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NCT02427841
|
77:93:chronic_disease,107:131:chronic_disease,133:148:chronic_disease,159:177:chronic_disease,182:201:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
| 1
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NCT02160288
|
7:18:treatment
|
Prior proctectomy
| 1
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0,
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NCT02234934
|
20:40:chronic_disease,42:53:chronic_disease,55:66:chronic_disease,68:71:chronic_disease,73:83:chronic_disease,85:99:chronic_disease,103:116:chronic_disease,,,165:173:treatment
|
Evidence of active infection with HIV-1, hepatitis B, Hepatitis C, CMV, adenovirus, parvovirus B19 or toxoplasmosis by DNA PCR within 8 weeks prior to mobilization/pheresis or bone marrow harvest
| 1
|
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NCT02003690
|
22:47:treatment
|
willing to engage in pharmacotherapy treatment at the CABS specialty clinic
| 1
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NCT00881660
|
24:79:chronic_disease
|
Confirmed diagnosis of severe or extremely severe left, right or bilateral CDH of the fetus
| 1
|
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NCT01618357
|
19:42:treatment
|
not have received prior radiation therapy to the involved breast at any time for any reason
| 1
|
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NCT03104725
|
19:50:treatment,58:76:treatment,78:83:treatment
|
Already taking an anti-oxidant dietary supplement (e.g., Olive Leaf Extract, MitoQ)
| 1
|
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NCT02771626
|
1:58:chronic_disease
|
Active known or suspected exclusionary autoimmune disease
| 1
|
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2,
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NCT01312857
|
41:64:treatment
|
However, patients who have responded to prior anti-EGFR therapy are eligible
| 1
|
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NCT02419560
|
22:46:treatment
|
Must be referred for treatment with ibrutinib
| 1
|
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0,
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NCT02132598
|
26:40:chronic_disease,44:63:chronic_disease,,109:118:treatment
|
Concurrent uncompensated hypothyroidism or thyroid dysfunction within 7 days before the first dose of study treatment
| 1
|
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NCT01568177
|
1:13:chronic_disease
|
endocarditis
| 1
|
[
"endocarditis"
] |
[
2
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NCT01572480
|
14:34:chronic_disease,77:93:chronic_disease,107:131:chronic_disease,133:148:chronic_disease,159:177:chronic_disease,182:201:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations
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NCT02533674
|
1:35:cancer
|
Non-small cell lung cancer (NSCLC)
| 1
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NCT03122912
|
13:20:allergy_name,22:33:allergy_name,35:42:allergy_name,46:53:allergy_name
|
Allergic to soybean, soybean oil, peanuts or seafood
| 1
|
[
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NCT02526511
|
19:42:cancer,19:29:cancer,85:105:cancer,,154:156:treatment,160:163:treatment
|
For patients with metastatic renal tumors to be enrolled, a histologic diagnosis of renal cell carcinoma must exist and any burden of disease >= 1 cm by CT or MRI is acceptable; the metastatic sites may be kidney, intra-abdominal (such as liver), brain, bone, or lymph nodes; lung lesions are NOT eligible because of the motion artifact caused by respiration
| 1
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NCT02703272
|
25:34:allergy_name,36:52:allergy_name,72:81:allergy_name
|
Participants with known allergies, hypersensitivity, or intolerance to ibrutinib or its excipients (refer to Investigator's Brochure)
| 1
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NCT02682407
|
21:55:chronic_disease
|
Have a diagnosis of human immunodeficiency virus (HIV)
| 1
|
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NCT01794793
|
58:67:treatment
|
Willingness and ability to comply with scheduled visits, treatment plans and any other study procedures
| 1
|
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NCT02160288
|
10:27:treatment
|
Previous radiation therapy to the anal canal and rectum
| 1
|
[
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"anal",
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0,
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0,
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0,
0,
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0
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NCT03037879
|
,,44:52:chronic_disease
|
Pre-screen MoCA score of < 22 (to rule out dementia)
| 1
|
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NCT00432094
|
,,55:65:treatment
|
Total Collection of ≥ 4 x 10^6 CD34 cells/kg prior to transplant one
| 1
|
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NCT02437851
|
49:59:cancer
|
Participants must not have any other concurrent malignancy
| 1
|
[
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0,
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0,
0,
0,
3
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NCT02776059
|
27:52:chronic_disease
|
uncontrolled recent upper gastrointestinal bleeding
| 1
|
[
"uncontrolled",
"recent",
"upper",
"gastrointestinal",
"bleeding"
] |
[
0,
0,
0,
2,
2
] |
NCT02138214
|
19:29:cancer
|
Concurrent active malignancy of another type
| 1
|
[
"Concurrent",
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"malignancy",
"of",
"another",
"type"
] |
[
0,
0,
3,
0,
0,
0
] |
NCT02339922
|
1:22:treatment,
|
platelet transfusions to help patients meet eligibility criteria are not allowed within 3 days before study enrollment
| 1
|
[
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NCT01861106
|
174:183:treatment
|
Should a patient have progressive disease, or a donor becomes not available after enrollment, the patient will be referred back to their primary hematologist-oncologist for treatment
| 1
|
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NCT02407171
|
8:26:chronic_disease,37:55:treatment,,174:191:treatment,195:219:treatment
|
active autoimmune disease requiring systemic treatment within the past 3 months or a documented history of clinically severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents
| 1
|
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NCT02584270
|
28:65:treatment
|
Patients with a history of prior head and neck radiation therapy
| 1
|
[
"Patients",
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NCT02776761
|
,58:76:treatment
|
Administration of chronic (defined as more than 14 days) immunosuppressants
| 1
|
[
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
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1
] |
NCT02671435
|
25:53:treatment
|
Subjects must be at the recurrent/metastatic setting
| 1
|
[
"Subjects",
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"recurrent/metastatic",
"setting"
] |
[
0,
0,
0,
0,
0,
1,
1
] |
NCT02907944
|
11:14:chronic_disease
|
Receiving HIV care in the index clinic
| 1
|
[
"Receiving",
"HIV",
"care",
"in",
"the",
"index",
"clinic"
] |
[
0,
2,
0,
0,
0,
0,
0
] |
NCT02339233
|
1:13:chronic_disease
|
dysautonomia that would contraindicate standing
| 1
|
[
"dysautonomia",
"that",
"would",
"contraindicate",
"standing"
] |
[
2,
0,
0,
0,
0
] |
NCT02050113
|
20:30:cancer
|
Patient has active malignancy
| 1
|
[
"Patient",
"has",
"active",
"malignancy"
] |
[
0,
0,
0,
3
] |
NCT02285114
|
4:27:chronic_disease,
|
No opportunistic infection within 30 days of study entry (at baseline/Day 1)
| 1
|
[
"No",
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"of",
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"at",
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0,
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0,
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0,
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0,
0,
0
] |
NCT02555280
|
1:11:chronic_disease
|
osteopenia
| 1
|
[
"osteopenia"
] |
[
2
] |
NCT03060772
|
1:4:chronic_disease
|
HIV-positive
| 1
|
[
"HIV-positive"
] |
[
2
] |
NCT01865162
|
,,62:75:treatment
|
Failure to recover from <CTCAE grade 2 toxicities related to prior therapy
| 1
|
[
"Failure",
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"from",
"<",
"CTCAE",
"grade",
"2",
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"prior",
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[
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT03107039
|
14:24:chronic_disease
|
Experiencing depression symptoms and generally healthy
| 1
|
[
"Experiencing",
"depression",
"symptoms",
"and",
"generally",
"healthy"
] |
[
0,
2,
0,
0,
0,
0
] |
NCT01989546
|
5:29:chronic_disease
|
Any gastrointestinal disease which would impair ability to swallow, retain, or absorb drug is not allowed
| 1
|
[
"Any",
"gastrointestinal",
"disease",
"which",
"would",
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"to",
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",",
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",",
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03053908
|
,,74:82:chronic_disease
|
History of a first-degree family member with early onset (age <60 years) dementia
| 1
|
[
"History",
"of",
"a",
"first-degree",
"family",
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"with",
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"age",
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT03037879
|
1:27:chronic_disease
|
Acute illness or infection
| 1
|
[
"Acute",
"illness",
"or",
"infection"
] |
[
2,
2,
2,
2
] |
NCT01653080
|
12:20:chronic_disease
|
History of diabetes
| 1
|
[
"History",
"of",
"diabetes"
] |
[
0,
0,
2
] |
NCT02856594
|
24:42:treatment
|
Scheduled for a second surgical procedure during hospital stay
| 1
|
[
"Scheduled",
"for",
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"second",
"surgical",
"procedure",
"during",
"hospital",
"stay"
] |
[
0,
0,
0,
0,
1,
1,
0,
0,
0
] |
NCT02474199
|
,,54:80:treatment
|
Clinical evidence of viral syndrome less than 7 days prior to darTregs infusion
| 1
|
[
"Clinical",
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"viral",
"syndrome",
"less",
"than",
"7",
"days",
"prior",
"to",
"darTregs",
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] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
1
] |
NCT02593123
|
1:44:treatment
|
Previous therapeutic radiation therapy (RT) that exceeds critical structure tolerance doses as determined by a radiation oncologist
| 1
|
[
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0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02072356
|
,,117:126:treatment
|
Evidence of potential delivery of greater than 16.5 mCi (30 Gy absorbed dose) of radiation to the lungs in a single treatment
| 1
|
[
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0,
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0,
1
] |
NCT03008070
|
,32:44:treatment,,
|
Have a stable weight since the liver biopsy was performed defined by no more than a 5 % loss of initial body weight
| 1
|
[
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0,
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0,
0,
0,
0,
0,
0,
0
] |
NCT03075761
|
21:40:allergy_name
|
Contraindication to increasing activity
| 1
|
[
"Contraindication",
"to",
"increasing",
"activity"
] |
[
0,
0,
4,
4
] |
NCT01464034
|
1:15:chronic_disease
|
POEMS syndrome
| 1
|
[
"POEMS",
"syndrome"
] |
[
2,
2
] |
NCT02316574
|
30:39:treatment
|
Agree to not seek additional treatment
| 1
|
[
"Agree",
"to",
"not",
"seek",
"additional",
"treatment"
] |
[
0,
0,
0,
0,
0,
1
] |
NCT03067571
|
11:55:chronic_disease,,
|
has known chronic obstructive pulmonary disease (COPD) with a forced expiratory volume in 1 second (FEV1) < 50% of predicted normal
| 1
|
[
"has",
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NCT01625923
|
12:29:chronic_disease
|
History of renal dysfunction
| 1
|
[
"History",
"of",
"renal",
"dysfunction"
] |
[
0,
0,
2,
2
] |
NCT02267863
|
14:36:chronic_disease,38:66:chronic_disease,125:143:chronic_disease
|
Uncontrolled leptomeningeal disease, auto-immune hemolytic anemia and uncontrolled and clinical significant disease related metabolic disorder
| 1
|
[
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] |
NCT02401035
|
,,,88:120:treatment,164:168:chronic_disease,314:328:treatment,
|
Subjects aged 1 to 16 years who in the judgment of the investigator are candidates for gastric acid suppression therapy (ie, those with a presumptive diagnosis of GERD, a clinical diagnosis of suspected GERD, symptomatic GERD, or endoscopically proven GERD) and whom the investigator judges would need to receive IV PPI therapy for at least 4 days
| 1
|
[
"Subjects",
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NCT02393794
|
26:36:cancer
|
Subject has a concurrent malignancy
| 1
|
[
"Subject",
"has",
"a",
"concurrent",
"malignancy"
] |
[
0,
0,
0,
0,
3
] |
NCT01941316
|
40:62:treatment,117:122:cancer,163:181:cancer
|
Patients who received primary curative chemoradiation therapy for limited disease, but who recur within the primary tumor site, previously radiated field or with distant metastases
| 1
|
[
"Patients",
"who",
"received",
"primary",
"curative",
"chemoradiation",
"therapy",
"for",
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"site",
",",
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3,
3
] |
NCT02589522
|
102:108:allergy_name
|
History of allergic reactions attributed to compounds of similar chemical or biologic composition to VX-970
| 1
|
[
"History",
"of",
"allergic",
"reactions",
"attributed",
"to",
"compounds",
"of",
"similar",
"chemical",
"or",
"biologic",
"composition",
"to",
"VX-970"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4
] |
NCT02578901
|
10:33:chronic_disease
|
Acquired storage pool deficiency
| 1
|
[
"Acquired",
"storage",
"pool",
"deficiency"
] |
[
0,
2,
2,
2
] |
NCT01547429
|
1:29:chronic_disease
|
Chronic or recurrent uveitis or history of the same
| 1
|
[
"Chronic",
"or",
"recurrent",
"uveitis",
"or",
"history",
"of",
"the",
"same"
] |
[
2,
2,
2,
2,
0,
0,
0,
0,
0
] |
NCT02401074
|
5:14:treatment,,
|
Pre-albuterol forced expiratory volume in the first second (FEV1) of >70% of the predicted value
| 1
|
[
"Pre-albuterol",
"forced",
"expiratory",
"volume",
"in",
"the",
"first",
"second",
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"FEV1",
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"of",
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"70",
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"of",
"the",
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] |
[
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01737502
|
1:16:chronic_disease
|
Angina pectoris
| 1
|
[
"Angina",
"pectoris"
] |
[
2,
2
] |
NCT02407028
|
21:24:chronic_disease,,,
|
Present with severe TBI, defined as GCS of 3 to 8
| 1
|
[
"Present",
"with",
"severe",
"TBI",
",",
"defined",
"as",
"GCS",
"of",
"3",
"to",
"8"
] |
[
0,
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02520778
|
15:34:cancer,46:51:cancer,69:104:treatment,185:193:cancer,197:220:cancer
|
Patients with active malignancies other than NSCLC or patients with prior curatively treated malignancy at high risk of relapse during the study period with the exception of localized squamous or basal cell skin cancers
| 1
|
[
"Patients",
"with",
"active",
"malignancies",
"other",
"than",
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"or",
"patients",
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0,
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0,
0,
0,
0,
0,
0,
0,
3,
0,
3,
3,
3,
3
] |
NCT02567227
|
13:21:chronic_disease
|
Presence of dementia
| 1
|
[
"Presence",
"of",
"dementia"
] |
[
0,
0,
2
] |
NCT02554253
|
1:26:chronic_disease
|
immunodeficiency syndrome
| 1
|
[
"immunodeficiency",
"syndrome"
] |
[
2,
2
] |
NCT03154567
|
144:153:treatment
|
Candidates must meet DSM-5 criteria for Mild-to-Moderate Cannabis Use Disorder (CUD) and be willing to participate in research but not seeking treatment
| 1
|
[
"Candidates",
"must",
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"criteria",
"for",
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"Cannabis",
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"willing",
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"in",
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] |
[
0,
0,
0,
0,
0,
0,
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02979574
|
10:26:treatment,28:35:treatment,37:49:treatment,58:70:treatment,,140:157:treatment
|
Complete active treatment (surgery, chemotherapy, and/or radiotherapy) at least one month prior to study initiation (patients on continued hormone treatment will not be excluded)
| 1
|
[
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0
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NCT03034213
|
19:33:chronic_disease,43:52:chronic_disease,54:64:chronic_disease,68:84:chronic_disease
|
Any other type of ventral hernia, such as umbilical, epigastric or Spigelian hernia
| 1
|
[
"Any",
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"type",
"of",
"ventral",
"hernia",
",",
"such",
"as",
"umbilical",
",",
"epigastric",
"or",
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[
0,
0,
0,
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2,
0,
0,
0,
2,
0,
2,
0,
2,
2
] |
NCT02562235
|
1:26:chronic_disease
|
Connective tissue disease
| 1
|
[
"Connective",
"tissue",
"disease"
] |
[
2,
2,
2
] |
NCT02192359
|
44:52:cancer
|
Imaging studies show evidence of recurrent tumor(s)
| 1
|
[
"Imaging",
"studies",
"show",
"evidence",
"of",
"recurrent",
"tumor",
"(",
"s",
")"
] |
[
3,
3,
3,
3,
3,
3,
3,
3,
3,
3
] |
NCT02834780
|
26:43:chronic_disease,52:69:chronic_disease,73:90:chronic_disease
|
Uncontrolled significant active infections, except Hepatitis B (HBV) or Hepatitis C (HCV)
| 1
|
[
"Uncontrolled",
"significant",
"active",
"infections",
",",
"except",
"Hepatitis",
"B",
"(",
"HBV",
")",
"or",
"Hepatitis",
"C",
"(",
"HCV",
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] |
[
0,
0,
2,
2,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02525861
|
,63:88:treatment,98:122:treatment,,158:168:treatment,190:211:treatment,213:225:treatment,227:243:treatment,249:258:treatment
|
The participant is receiving or requires long-term (>4 weeks) immunosuppressive therapy, such as systemic corticosteroids at doses greater than 10 mg/day of prednisone (or its equivalent), mycophenolate mofetil, azathioprine, cyclophosphamide, and rituximab
| 1
|
[
"The",
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"4",
"weeks",
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",",
"such",
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")",
",",
"mycophenolate",
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",",
"azathioprine",
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"cyclophosphamide",
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0,
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0,
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0,
1,
1,
0,
1,
0,
1,
0,
0,
1
] |
NCT02276716
|
14:35:chronic_disease
|
Diagnosis of familial dysautonomia (with mutation testing)
| 1
|
[
"Diagnosis",
"of",
"familial",
"dysautonomia",
"(",
"with",
"mutation",
"testing",
")"
] |
[
0,
0,
2,
2,
0,
0,
0,
0,
0
] |
NCT02514083
|
1:4:cancer,6:21:chronic_disease,52:55:cancer,
|
SLL: lymphadenopathy with the tissue morphology of CLL but that are not leukemic, < 5,000 cells/microL
| 1
|
[
"SLL",
":",
"lymphadenopathy",
"with",
"the",
"tissue",
"morphology",
"of",
"CLL",
"but",
"that",
"are",
"not",
"leukemic",
",",
"<",
"5,000",
"cells/microL"
] |
[
3,
0,
2,
0,
0,
0,
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02070549
|
1:31:cancer,108:118:cancer,162:167:cancer
|
Hepatocellular carcinoma (HCC) patients are not required to have histologically or cytologically confirmed malignancy, patients are considered eligible based on tumor markers and/or imaging assessment
| 1
|
[
"Hepatocellular",
"carcinoma",
"(",
"HCC",
")",
"patients",
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"to",
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",",
"patients",
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"based",
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"imaging",
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[
3,
3,
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0,
0,
0,
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3,
0,
0,
0,
0,
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0,
0,
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0,
0,
0,
0
] |
NCT02025465
|
1:14:chronic_disease,32:45:chronic_disease,,,,,143:197:chronic_disease,201:222:chronic_disease
|
Heart failure and a history of heart failure with an ejection fraction of 40-50% may occur with a normal ejection fraction now referred to as Heart Failure With Preserved Ejection Fraction (HFpEF) or diastolic dysfunction
| 1
|
[
"Heart",
"failure",
"and",
"a",
"history",
"of",
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"failure",
"with",
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"%",
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"with",
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"Failure",
"With",
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"Ejection",
"Fraction",
"(",
"HFpEF",
")",
"or",
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[
2,
2,
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2,
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0,
0,
0,
0,
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NCT02231073
|
19:29:treatment
|
Recent changes in medication
| 1
|
[
"Recent",
"changes",
"in",
"medication"
] |
[
0,
0,
0,
1
] |
NCT02078102
|
33:50:treatment,
|
Patients must not have received radiation therapy within the past 4 weeks
| 1
|
[
"Patients",
"must",
"not",
"have",
"received",
"radiation",
"therapy",
"within",
"the",
"past",
"4",
"weeks"
] |
[
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0
] |
NCT02397889
|
46:60:treatment,65:82:treatment,89:104:treatment,114:127:treatment,131:138:treatment,
|
Patients who report current treatment with a benzodiazepine, an opioid medication, or a mood stabilizer (such as valproic acid or lithium) within 2 weeks prior to randomization
| 1
|
[
"Patients",
"who",
"report",
"current",
"treatment",
"with",
"a",
"benzodiazepine",
",",
"an",
"opioid",
"medication",
",",
"or",
"a",
"mood",
"stabilizer",
"(",
"such",
"as",
"valproic",
"acid",
"or",
"lithium",
")",
"within",
"2",
"weeks",
"prior",
"to",
"randomization"
] |
[
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
1,
1,
0,
0,
0,
1,
1,
0,
0,
0,
1,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02538198
|
13:23:chronic_disease,
|
Significant neuropathy ≥Grade 3 at baseline
| 1
|
[
"Significant",
"neuropathy",
"≥Grade",
"3",
"at",
"baseline"
] |
[
0,
2,
0,
0,
0,
0
] |
NCT01895777
|
1:18:chronic_disease
|
Renal dysfunction
| 1
|
[
"Renal",
"dysfunction"
] |
[
2,
2
] |
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