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NCT02169037
|
115:137:treatment
|
willingness, ability and commitment to participate in baseline and follow-up evaluations without participation in another clinical trial (unless documented approval received from both sponsors)
| 1
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NCT02476409
|
54:90:chronic_disease,203:216:chronic_disease,252:267:chronic_disease
|
Patients with the following predisposing factors for osmotic demyelinating syndrome (ODS), assessed by the study investigator judgment, will be excluded: chronic alcoholism at the time of study, severe liver disease, marked malnutrition, and risk for chronic hypoxia
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NCT03001830
|
1:11:cancer
|
malignancy
| 1
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NCT02335242
|
29:66:treatment,76:88:treatment,90:102:treatment,104:116:treatment,118:128:treatment,153:162:treatment
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Requires concomitant use of potent cytochrome P450 3A4 inhibitors (such as ketoconazole, itraconazole, erythromycin, saquinavir), or concomitant use of ritonavir
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NCT00703105
|
37:64:treatment,68:81:treatment,,111:116:cancer
|
Patients must not have received any antineoplastic chemotherapy or immunotherapy for the four weeks preceding tumor excision
| 1
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NCT02799095
|
59:70:cancer
|
the subject has histological or cytological evidence of a solid tumor
| 1
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NCT02124772
|
1:31:treatment
|
prior treatment with sorafenib
| 1
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NCT01811368
|
18:51:treatment
|
Patients fit for non-myeloablative transplantation or best treatment that have an available matched (9/10 or better) related or unrelated donor
| 1
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NCT01994382
|
21:40:cancer
|
Prior treatment for lymphoid malignancy for progressive /refractory disease
| 1
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NCT02503722
|
4:13:treatment,39:47:treatment,49:56:treatment,61:82:treatment,88:103:treatment
|
be treatment naive for 3rd generation EGFR-TKI (CO-1686 and osimertinib [AZD9291]) and mTOR inhibitors
| 1
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NCT02912572
|
33:45:treatment
|
patients who have only received chemotherapy in the adjuvant setting
| 1
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NCT01389024
|
51:59:treatment
|
The parents or guardians must provide consent for sedation
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NCT02341235
|
1:8:treatment,
|
Surgery in the past six months
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NCT01980823
|
10:22:treatment,24:41:treatment,46:62:treatment,
|
No prior chemotherapy, radiation therapy, or breast resection within 6 months of study entry
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NCT02025543
|
21:47:treatment
|
contraindication to magnetic resonance imaging
| 1
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NCT02152254
|
26:38:treatment,40:47:treatment,52:64:treatment,,127:136:treatment,150:161:treatment,165:186:treatment
|
The patient has received chemotherapy, surgery, or radiotherapy (for therapeutic purposes) within 3 weeks of initiating study treatment (4 weeks for bevacizumab or investigational drugs)
| 1
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NCT02446093
|
1:13:treatment
|
valacyclovir
| 1
|
[
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[
1
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NCT02646930
|
63:74:treatment,83:94:treatment,99:135:treatment,139:154:treatment,200:218:treatment,
|
Post-enrollment exclusion will include patients receiving any antibiotics, except prophylaxis for transvaginal oocyte retrieval (TVOR) or glucocorticoids, except nasal preparations, from the time of endometrial biopsy until initial transvaginal ultrasound (TVUS) for pregnancy
| 1
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NCT02226341
|
38:43:chronic_disease,45:52:chronic_disease,54:67:chronic_disease,69:85:chronic_disease,87:96:chronic_disease,98:105:chronic_disease,110:130:chronic_disease,338:341:chronic_disease
|
Severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, pulmonary, cardiac, or neurological disease (or, in the investigator's opinion, any other concomitant medical condition that places the participant at risk by participating in this study) with the exception of diseases or conditions related to active SLE
| 1
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NCT01726257
|
32:54:treatment
|
Participating in enrollment of another clinical study
| 1
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NCT02442323
|
1:19:cancer
|
mucinous carcinoma
| 1
|
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NCT01928576
|
,57:69:treatment,,102:111:treatment,116:137:cancer
|
Patients must have received at least one platinum based chemotherapy, and not more than three, prior therapies for stage IIIB/IV disease
| 1
|
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NCT02607514
|
1:19:chronic_disease,62:79:chronic_disease,81:103:chronic_disease,105:117:chronic_disease,,,,156:167:chronic_disease,,223:246:chronic_disease,328:348:chronic_disease,350:360:cancer,365:386:chronic_disease
|
Medical conditions that may make participation unsafe (e.g., diabetes [I & II], cardiovascular disease, hypertension [>140 systolic and/or >90 diastolic], hypotension [<90 systolic and/or <60 diastolic, during screening], orthostatic hypotension [systolic drop of 20 points or 10 point diastolic or heart rate increase by 10], autoimmune disorders, malignancy, or autonomic dysfunction)
| 1
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NCT02475707
|
44:102:treatment
|
Only patients who receive infusions in the integrated Cell and Gene Therapy (CAGT) Transplant program at Texas Children's Hospital (TCH) or Houston Methodist Hospital (HMH)
| 1
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NCT03028350
|
5:32:treatment,62:74:treatment,76:88:treatment,90:103:treatment,105:115:treatment,117:121:treatment,123:136:treatment,138:151:treatment,153:171:treatment,173:185:treatment,191:207:treatment,
|
Any immunosuppressive treatment including but not limited to methotrexate, cyclosporine, mycophenolate, tacrolimus, gold, penicillamine, sulfasalazine, hydroxychloroquine, azathioprine, and cyclophosphamide in the last two weeks before starting treatment
| 1
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NCT02920710
|
17:46:treatment
|
Stable baseline immunosuppressive medications
| 1
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NCT02563574
|
13:21:chronic_disease
|
Evidence of dementia
| 1
|
[
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NCT02353819
|
16:26:cancer,
|
Prior invasive malignancy unless disease free for a minimum of 3 years
| 1
|
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NCT02320292
|
19:31:treatment
|
No indication for chemotherapy
| 1
|
[
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NCT02048371
|
5:15:chronic_disease,,,
|
Any hemorrhage or bleeding event ≥ NCI CTCAE Grade 3 within 4 weeks prior to study registration
| 1
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NCT02061761
|
20:31:treatment,33:36:cancer,38:40:cancer,42:45:cancer
|
For dose expansion monotherapy: CLL, HL, NHL
| 1
|
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NCT01243931
|
6:23:chronic_disease
|
Deep corneal opacities and irregularities
| 1
|
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0,
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NCT01983462
|
4:21:treatment,29:36:treatment,38:46:treatment,49:56:treatment,58:69:treatment,72:79:treatment,81:101:treatment,115:143:treatment,
|
On weight loss drugs (e.g., Xenical (orlistat), Meridia (sibutramine), Acutrim (phenylpropanol-amine), or similar over-the-counter medications) within 3 months of screening
| 1
|
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NCT02344355
|
7:10:chronic_disease
|
Known HIV-positive individuals
| 1
|
[
"Known",
"HIV-positive",
"individuals"
] |
[
0,
2,
0
] |
NCT01737502
|
1:20:chronic_disease
|
labile hypertension
| 1
|
[
"labile",
"hypertension"
] |
[
2,
2
] |
NCT02128100
|
1:4:chronic_disease
|
HIV testing is not manditory for this protocol
| 1
|
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0,
0,
0
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NCT02437851
|
7:16:treatment,24:33:chronic_disease,45:73:chronic_disease,78:109:chronic_disease,
|
Acute treatment for an infection (excluding fungal infection of the skin and sexually transmitted infections) or other serious medical illness within 2 weeks before enrollment
| 1
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NCT02383979
|
50:54:treatment
|
Cooperative, with time and availability to do an fMRI
| 1
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NCT02518594
|
18:46:treatment,
|
Participation in another interventional study that influences gestational age at delivery or neonatal morbidity or mortality
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NCT00788164
|
15:19:allergy_name
|
No allergy to eggs
| 1
|
[
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[
0,
0,
0,
4
] |
NCT03112824
|
1:25:treatment
|
anti-insomnia medication on a regular basis
| 1
|
[
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] |
[
1,
1,
0,
0,
0,
0
] |
NCT02567422
|
1:10:cancer
|
Carcinoma of the neck of unknown primary site origin (regardless of HPV/p16 status)
| 1
|
[
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NCT02981069
|
30:64:chronic_disease,,,,,,,
|
Individuals with evidence of proliferative diabetic retinopathy, plasma creatinine >1.4 females or >1.5 males, or 24-hour urine albumin excretion > 300 mg will be excluded
| 1
|
[
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NCT02393885
|
23:66:treatment,79:91:chronic_disease,93:113:chronic_disease,118:127:chronic_disease
|
Documented history of previous catheter ablation with perforation, history of pericarditis, pericardial effusion, or tamponade
| 1
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NCT02189889
|
1:7:chronic_disease,11:21:chronic_disease,42:55:treatment
|
sepsis or bacteremia defined by positive blood culture
| 1
|
[
"sepsis",
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[
2,
0,
2,
0,
0,
0,
1,
1
] |
NCT01893554
|
14:25:treatment,41:62:treatment,67:80:chronic_disease,,117:128:treatment,165:184:treatment
|
Has received antibiotics or systemic or nasal steroid therapy for acute illness within the previous 3 days prior to vaccination (steroid skin creams or lotions and topical antibiotics or antifungal preparations are permitted)
| 1
|
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NCT00358657
|
14:48:chronic_disease
|
Positive for human immunodeficiency virus (HIV)
| 1
|
[
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[
0,
0,
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2,
2,
2,
0,
0
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NCT02562235
|
1:13:treatment,,
|
Pretreatment with NO donors (e.g. nitrates) within the last 2-weeks before visit 1
| 1
|
[
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0,
0,
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] |
NCT02140255
|
26:29:chronic_disease,
|
Two consecutive negative HIV antibody tests by fourth generation enzyme-linked immunosorbent assay (ELISA) (performed in the study's designated central laboratory) at least 8 weeks apart
| 1
|
[
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NCT02953509
|
1:4:chronic_disease
|
HIV
| 1
|
[
"HIV"
] |
[
2
] |
NCT02822599
|
53:71:treatment
|
Neonatal and infant cardiac patients presenting for open-heart surgery at Nicklaus Children's Hospital
| 1
|
[
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[
0,
0,
0,
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0,
0,
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1,
1,
0,
0,
0,
0,
0
] |
NCT02657993
|
1:30:treatment,
|
Non-steroidal joint injection within the last 3 months
| 1
|
[
"Non-steroidal",
"joint",
"injection",
"within",
"the",
"last",
"3",
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] |
[
1,
1,
1,
0,
0,
0,
0,
0
] |
NCT02519322
|
1:25:cancer,
|
oligometastatic melanoma is defined as three or fewer areas of resectable disease excluding central nervous system and bone involvement
| 1
|
[
"oligometastatic",
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"bone",
"involvement"
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[
3,
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0,
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01760655
|
1:23:cancer
|
Acute myeloid leukemia with high risk features
| 1
|
[
"Acute",
"myeloid",
"leukemia",
"with",
"high",
"risk",
"features"
] |
[
3,
3,
3,
0,
0,
0,
0
] |
NCT02400463
|
7:10:chronic_disease
|
known HIV infection
| 1
|
[
"known",
"HIV",
"infection"
] |
[
0,
2,
0
] |
NCT02268253
|
42:59:chronic_disease,67:104:chronic_disease,106:128:chronic_disease
|
has uncontrolled, clinically significant pulmonary disease (e.g., chronic obstructive pulmonary disease, pulmonary hypertension) that, in the Investigator's opinion, would put the patient at significant risk for pulmonary complications during the study
| 1
|
[
"has",
"uncontrolled",
",",
"clinically",
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"e.g.",
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NCT02237183
|
46:54:treatment
|
Participants must not have been treated with iloprost at any time
| 1
|
[
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[
0,
0,
0,
0,
0,
0,
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0,
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] |
NCT00483249
|
58:89:treatment
|
Anticipated mortality comparable to published rates with conventional surgical treatment
| 1
|
[
"Anticipated",
"mortality",
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"to",
"published",
"rates",
"with",
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"surgical",
"treatment"
] |
[
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02400463
|
25:41:cancer
|
tissue demonstration of hemophagocytosis
| 1
|
[
"tissue",
"demonstration",
"of",
"hemophagocytosis"
] |
[
0,
0,
0,
3
] |
NCT02367040
|
1:18:chronic_disease,14:17:chronic_disease,22:39:chronic_disease,35:38:chronic_disease,159:189:treatment
|
Hepatitis B (HBV) or hepatitis C (HCV). Patients positive for HBsAg or HBcAb will be eligible if they are negative for HBV-DNA, these patients should receive prophylactic antiviral therapy. Patients positive for anti- HCV antibody will be eligible if they are negative for HCV-RNA
| 1
|
[
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"HCV",
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NCT03181126
|
,73:85:treatment
|
Refractory is defined as persistent disease after at least 2 courses of chemotherapy
| 1
|
[
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[
0,
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0,
0,
0,
0,
0,
0,
0,
0,
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] |
NCT02271919
|
15:24:treatment
|
Interested in treatment that might change smoking behavior
| 1
|
[
"Interested",
"in",
"treatment",
"that",
"might",
"change",
"smoking",
"behavior"
] |
[
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT03011684
|
5:18:cancer
|
New breast cancer diagnosis
| 1
|
[
"New",
"breast",
"cancer",
"diagnosis"
] |
[
0,
3,
3,
0
] |
NCT03043794
|
1:15:treatment
|
Breast implant in the involved breast
| 1
|
[
"Breast",
"implant",
"in",
"the",
"involved",
"breast"
] |
[
1,
1,
0,
0,
0,
0
] |
NCT02857218
|
40:51:allergy_name
|
a known history of hypersensitivity to ferumoxytol
| 1
|
[
"a",
"known",
"history",
"of",
"hypersensitivity",
"to",
"ferumoxytol"
] |
[
0,
0,
0,
0,
0,
0,
4
] |
NCT03138733
|
1:54:chronic_disease,130:142:treatment,146:155:treatment
|
Bloodstream or non-bloodstream concomitant infections with Gram-negative bacteria that are known to be non-susceptible to either ceftobiprole or aztreonam
| 1
|
[
"Bloodstream",
"or",
"non-bloodstream",
"concomitant",
"infections",
"with",
"Gram-negative",
"bacteria",
"that",
"are",
"known",
"to",
"be",
"non-susceptible",
"to",
"either",
"ceftobiprole",
"or",
"aztreonam"
] |
[
2,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1
] |
NCT02898597
|
12:36:chronic_disease,44:57:chronic_disease,62:78:chronic_disease
|
History of serious mental illnesses (e.g., schizophrenia and bipolar disorder)
| 1
|
[
"History",
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"mental",
"illnesses",
"(",
"e.g.",
",",
"schizophrenia",
"and",
"bipolar",
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")"
] |
[
0,
0,
2,
2,
2,
0,
0,
0,
2,
0,
2,
2,
0
] |
NCT02209636
|
8:17:treatment,37:47:treatment,49:61:treatment,63:78:treatment
|
Active vitamin D analogue use (i.e. calcitriol, paricalcitol, doxercalciferol)
| 1
|
[
"Active",
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"D",
"analogue",
"use",
"(",
"i.e",
".",
"calcitriol",
",",
"paricalcitol",
",",
"doxercalciferol",
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] |
[
0,
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1,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1,
0
] |
NCT02172651
|
102:111:allergy_name
|
History of allergic reactions attributed to compounds of similar chemical or biologic composition to vitamin D
| 1
|
[
"History",
"of",
"allergic",
"reactions",
"attributed",
"to",
"compounds",
"of",
"similar",
"chemical",
"or",
"biologic",
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[
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4,
4
] |
NCT02287337
|
26:35:treatment
|
Inability to comply with treatment and follow-up schedule
| 1
|
[
"Inability",
"to",
"comply",
"with",
"treatment",
"and",
"follow-up",
"schedule"
] |
[
0,
0,
0,
0,
1,
0,
0,
0
] |
NCT02273375
|
34:45:chronic_disease
|
Patients with a past or resolved hepatitis B infection (defined as presence of hepatitis B core antibody (anti-HBc) and absence of HBSAg) are eligible
| 1
|
[
"Patients",
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"B",
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"defined",
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"core",
"antibody",
"(",
"anti-HBc",
")",
"and",
"absence",
"of",
"HBSAg",
")",
"are",
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[
0,
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0,
0,
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0,
0,
0,
0,
0,
0,
0
] |
NCT02836574
|
54:67:treatment
|
anatomic abnormalities that would interfere with the NKA injection procedure
| 1
|
[
"anatomic",
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"that",
"would",
"interfere",
"with",
"the",
"NKA",
"injection",
"procedure"
] |
[
0,
0,
0,
0,
0,
0,
0,
1,
1,
0
] |
NCT02988960
|
48:88:cancer
|
Participant must not have a known uncontrolled malignancy of the central nervous system
| 1
|
[
"Participant",
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"have",
"a",
"known",
"uncontrolled",
"malignancy",
"of",
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"central",
"nervous",
"system"
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[
0,
0,
0,
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3,
3,
3,
3,
3
] |
NCT01409161
|
16:19:cancer,49:90:treatment,92:123:treatment,128:136:treatment
|
A diagnosis of APL based on the presence of the PML-RAR-alpha fusion gene by cytogenetics, polymerase chain reaction (PCR), or POD test
| 1
|
[
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"of",
"APL",
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0,
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1
] |
NCT02522715
|
,,61:70:allergy_name,72:86:allergy_name,141:153:allergy_name,165:173:allergy_name,175:199:allergy_name,205:229:allergy_name
|
History of severe hypersensitivity reaction (>= grade 3) to docetaxel, polysorbate 80 containing drugs, or any of the capsule components of enzalutamide, including Labrasol, butylated hydroxyanisole, and butylated hydroxytoluene
| 1
|
[
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0
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NCT02496611
|
12:24:chronic_disease
|
History of pancreatitis
| 1
|
[
"History",
"of",
"pancreatitis"
] |
[
0,
0,
2
] |
NCT02876302
|
26:28:cancer,30:32:cancer,38:42:cancer,61:97:cancer
|
Patients must have known ER, PR, and HER2 status defined as triple-negative breast cancer (TNBC)
| 1
|
[
"Patients",
"must",
"have",
"known",
"ER",
",",
"PR",
",",
"and",
"HER2",
"status",
"defined",
"as",
"triple-negative",
"breast",
"cancer",
"(",
"TNBC",
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[
0,
0,
0,
0,
3,
0,
3,
0,
0,
3,
0,
0,
0,
3,
3,
3,
3,
0,
0
] |
NCT03017118
|
1:30:chronic_disease
|
Post-traumatic osteoarthritis
| 1
|
[
"Post-traumatic",
"osteoarthritis"
] |
[
2,
2
] |
NCT02842658
|
1:16:chronic_disease
|
Unstable angina
| 1
|
[
"Unstable",
"angina"
] |
[
2,
2
] |
NCT02624258
|
21:32:chronic_disease,
|
Patients with prior CNS disease that has been effectively treated will be eligible providing treatment was >4 weeks before enrollment
| 1
|
[
"Patients",
"with",
"prior",
"CNS",
"disease",
"that",
"has",
"been",
"effectively",
"treated",
"will",
"be",
"eligible",
"providing",
"treatment",
"was",
">",
"4",
"weeks",
"before",
"enrollment"
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0,
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0,
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0,
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NCT02013154
|
1:6:cancer
|
Tumor tissue for mandatory evaluation
| 1
|
[
"Tumor",
"tissue",
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"evaluation"
] |
[
3,
0,
0,
0,
0
] |
NCT02669966
|
34:37:chronic_disease
|
The donor candidate must be anti-HCV positive by ELISA and HCV RNA negative by PCR, with both tests repeated for confirmation, as per standard protocol
| 1
|
[
"The",
"donor",
"candidate",
"must",
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"by",
"ELISA",
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",",
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0
] |
NCT02493530
|
18:52:chronic_disease
|
Known history of human immunodeficiency virus (HIV)
| 1
|
[
"Known",
"history",
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"human",
"immunodeficiency",
"virus",
"(",
"HIV",
")"
] |
[
0,
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT02013778
|
24:48:cancer,134:137:cancer,141:147:treatment,,300:303:treatment,307:309:treatment,,400:409:chronic_disease,417:436:chronic_disease,,
|
Patient diagnosed with hepatocellular carcinoma in both lobes of the liver by one of the following methods (Pathologically confirmed HCC by biopsy or HCC 2 cm with classic radiographic findings of arterial phase enhancement with venous phase washout and pseudocapsule formation on contrast enhanced MRI or CT or Lesion greater than 2 cm with probable imaging features of HCC and imaging findings of cirrhosis and/or portal hypertension or a serum alphafetoprotein (AFP) greater than 200 mg/mL
| 1
|
[
"Patient",
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"with",
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"in",
"both",
"lobes",
"of",
"the",
"liver",
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"of",
"the",
"following",
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"phase",
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"or",
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NCT02290951
|
52:64:allergy_name
|
History of hypersensitivity to any compound in the tetracycline antibiotics group
| 1
|
[
"History",
"of",
"hypersensitivity",
"to",
"any",
"compound",
"in",
"the",
"tetracycline",
"antibiotics",
"group"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
4,
0,
0
] |
NCT02635360
|
1:13:treatment
|
chemotherapy
| 1
|
[
"chemotherapy"
] |
[
1
] |
NCT02764853
|
1:4:chronic_disease
|
HIV-positive
| 1
|
[
"HIV-positive"
] |
[
2
] |
NCT03153410
|
33:45:treatment,
|
Must have received last dose of chemotherapy at least 14 days or longer prior to entry into the study
| 1
|
[
"Must",
"have",
"received",
"last",
"dose",
"of",
"chemotherapy",
"at",
"least",
"14",
"days",
"or",
"longer",
"prior",
"to",
"entry",
"into",
"the",
"study"
] |
[
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02660528
|
1:37:chronic_disease,,,
|
Abnormal thyroid-stimulating hormone (TSH <0.4 or >5.0mlU/L)
| 1
|
[
"Abnormal",
"thyroid-stimulating",
"hormone",
"(",
"TSH",
"<",
"0.4",
"or",
">",
"5.0mlU/L",
")"
] |
[
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02140255
|
15:19:treatment,
|
No receipt of ARVs during the current pregnancy
| 1
|
[
"No",
"receipt",
"of",
"ARVs",
"during",
"the",
"current",
"pregnancy"
] |
[
0,
0,
0,
1,
0,
0,
0,
0
] |
NCT02656706
|
15:30:chronic_disease,61:77:chronic_disease,,114:135:chronic_disease,
|
Patients with unstable angina (anginal symptoms at rest) or new-onset angina (began within the last 3 months) or myocardial infarction within the past 6 months
| 1
|
[
"Patients",
"with",
"unstable",
"angina",
"(",
"anginal",
"symptoms",
"at",
"rest",
")",
"or",
"new-onset",
"angina",
"(",
"began",
"within",
"the",
"last",
"3",
"months",
")",
"or",
"myocardial",
"infarction",
"within",
"the",
"past",
"6",
"months"
] |
[
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
0,
0,
0
] |
NCT02503358
|
33:42:treatment
|
Patients who progressed on such treatment, i.e., have developed acquired resistance and are no longer reasonably expected to derive therapeutic benefit are eligible for the trial
| 1
|
[
"Patients",
"who",
"progressed",
"on",
"such",
"treatment",
",",
"i.e.",
",",
"have",
"developed",
"acquired",
"resistance",
"and",
"are",
"no",
"longer",
"reasonably",
"expected",
"to",
"derive",
"therapeutic",
"benefit",
"are",
"eligible",
"for",
"the",
"trial"
] |
[
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02843945
|
1:13:treatment,,
|
Chemotherapy was administered for 2-6 cycles with any combination
| 1
|
[
"Chemotherapy",
"was",
"administered",
"for",
"2-6",
"cycles",
"with",
"any",
"combination"
] |
[
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01989585
|
14:34:chronic_disease,77:101:chronic_disease,115:139:chronic_disease,141:165:chronic_disease,167:185:chronic_disease,187:208:chronic_disease,213:232:chronic_disease,233:250:chronic_disease
|
Uncontrolled intercurrent illness including, but not limited to, ongoing or active serious infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled diabetes, or psychiatric illness/social situations that would limit compliance with study requirements
| 1
|
[
"Uncontrolled",
"intercurrent",
"illness",
"including",
",",
"but",
"not",
"limited",
"to",
",",
"ongoing",
"or",
"active",
"serious",
"infection",
",",
"symptomatic",
"congestive",
"heart",
"failure",
",",
"unstable",
"angina",
"pectoris",
",",
"cardiac",
"arrhythmia",
",",
"uncontrolled",
"diabetes",
",",
"or",
"psychiatric",
"illness/social",
"situations",
"that",
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"compliance",
"with",
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[
0,
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2,
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0,
2,
2,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT00720785
|
1:4:chronic_disease
|
HIV-positive patients
| 1
|
[
"HIV-positive",
"patients"
] |
[
2,
0
] |
NCT02342808
|
1:11:chronic_disease,,
|
Severe CKD (eGFR <40 ml/min/1.73m2)
| 1
|
[
"Severe",
"CKD",
"(",
"eGFR",
"<",
"40",
"ml/min/1.73m2",
")"
] |
[
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT02140255
|
11:14:chronic_disease
|
No plasma HIV RNA detected at the time of the second consecutive negative HIV DNA test (based on testing performed in the study's designated VQA-certified central laboratory)
| 1
|
[
"No",
"plasma",
"HIV",
"RNA",
"detected",
"at",
"the",
"time",
"of",
"the",
"second",
"consecutive",
"negative",
"HIV",
"DNA",
"test",
"(",
"based",
"on",
"testing",
"performed",
"in",
"the",
"study",
"'s",
"designated",
"VQA-certified",
"central",
"laboratory",
")"
] |
[
0,
0,
2,
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,
0,
0
] |
NCT00351611
|
,,25:44:treatment
|
Currently taking 1 to 3 antiepileptic drugs
| 1
|
[
"Currently",
"taking",
"1",
"to",
"3",
"antiepileptic",
"drugs"
] |
[
0,
0,
0,
0,
0,
1,
1
] |
NCT02335138
|
30:33:chronic_disease,
|
Willingness to be tested for HIV with one's male sexual partner
| 1
|
[
"Willingness",
"to",
"be",
"tested",
"for",
"HIV",
"with",
"one",
"'s",
"male",
"sexual",
"partner"
] |
[
0,
0,
0,
0,
0,
2,
0,
0,
0,
0,
0,
0
] |
NCT02541903
|
15:37:chronic_disease
|
Any active or uncontrolled infection
| 1
|
[
"Any",
"active",
"or",
"uncontrolled",
"infection"
] |
[
0,
0,
0,
2,
2
] |
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