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NCT02446236
|
39:95:treatment
|
Patients who have previously received high-dose chemotherapy with peripheral stem cell support
| 1
|
[
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NCT02388685
|
1:12:treatment,16:36:treatment,
|
angioplasty or lumbar sympathectomy within 3 months of enrollment
| 1
|
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NCT01829958
|
1:26:chronic_disease
|
Systemic fungal infection
| 1
|
[
"Systemic",
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[
2,
2,
2
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NCT02744430
|
,,,59:66:treatment
|
Single unilateral ureteral calculus 4 to 10 mm visible on CT scan within the ureter
| 1
|
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NCT02132598
|
38:61:treatment,63:86:treatment,91:126:treatment,121:125:treatment,176:193:treatment,
|
The subject is receiving concomitant treatment with warfarin, warfarin-related agents, or low molecular weight heparin (LMWH) at the time of study entry at therapeutic doses. Low-dose warfarin (≤ 1 mg/day) or LMWH at prophylactic doses
| 1
|
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NCT02451553
|
27:35:treatment,56:77:treatment,147:165:treatment,153:165:treatment
|
patients who already have OncoPlex or other equivalent gene sequencing assay (eg Foundation One, Perthera, Caris etc) test results available from prior tumor biopsy are eligible to participate, without the needed of a repeat tumor biopsy, but the test results need to be available to the study principal investigator
| 1
|
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NCT00719888
|
,142:159:treatment
|
these patients must be discussed with the PI prior to enrollment; patients persistently aplastic for greater than one month since completing last chemotherapy are also eligible with PI approval
| 1
|
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NCT02452008
|
31:36:cancer,37:43:treatment,87:96:treatment,118:126:treatment
|
Patients acceptance to have a tumor biopsy of an accessible lesion at baseline and on treatment if the lesion can be biopsied with acceptable clinical risk (as judged by the investigator)
| 1
|
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NCT01453088
|
1:38:chronic_disease,
|
Sensory peripheral neuropathy grade 4 within 14 days of enrollment
| 1
|
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NCT02269293
|
11:24:treatment,41:56:cancer,68:80:treatment,82:107:treatment,112:131:treatment,,186:195:treatment
|
Any other prior therapy directed at the malignant tumor, including chemotherapy, biologic/targeted therapy and immunologic therapy, must be discontinued at least 3 weeks prior to study treatment initiation
| 1
|
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NCT02192398
|
7:17:treatment,
|
Takes vitamin B2 > 1.6mg/day during the study
| 1
|
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NCT02789228
|
15:25:chronic_disease
|
Patients with active HIV
| 1
|
[
"Patients",
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"HIV"
] |
[
0,
0,
2,
2
] |
NCT02334865
|
17:35:chronic_disease
|
Must be free of systemic infection
| 1
|
[
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"infection"
] |
[
0,
0,
0,
0,
2,
2
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NCT01419561
|
1:21:chronic_disease
|
Altered mental state
| 1
|
[
"Altered",
"mental",
"state"
] |
[
2,
2,
2
] |
NCT03109431
|
1:4:chronic_disease
|
HIV-negative (high-risk HIV-negative youth will be invited to participate in another study)
| 1
|
[
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NCT02926729
|
14:39:treatment,41:51:treatment,56:65:treatment
|
Eligible for breast conserving surgery, lumpectomy and radiation
| 1
|
[
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NCT03033498
|
105:113:treatment
|
Consideration by the investigator for any reason that the subject is an unsuitable candidate to receive ABBV-951
| 1
|
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NCT03125226
|
1:10:treatment,,67:86:treatment,67:76:treatment,115:127:treatment
|
Treatment plan for bladder must include at least 4 weeks of daily radiation treatment (most patients will receive chemotherapy concurrent with radiation, but this is not required for trial enrollment)
| 1
|
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NCT02562430
|
30:54:treatment,
|
Patients must have either no antidepressant treatment or stable (for at least 4 weeks prior to screening)
| 1
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NCT01841333
|
21:33:chronic_disease,35:44:chronic_disease,55:64:chronic_disease,89:96:treatment
|
Active uncontrolled acute fungal, bacterial, or other infection that is unresponsive to therapy at time of study drug dosing
| 1
|
[
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NCT02512718
|
12:15:allergy_name,17:21:allergy_name,26:29:allergy_name,30:45:allergy_name
|
Allergy to egg, fish, or soy/legume products
| 1
|
[
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[
0,
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NCT02901067
|
27:56:allergy_name
|
Known contraindication to pharmacologic anticoagulation
| 1
|
[
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[
0,
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0,
4,
4
] |
NCT02910700
|
7:36:treatment,
|
other immunosuppressive medications within 14 days of study drug administration
| 1
|
[
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0,
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NCT02905578
|
97:131:treatment
|
If all of the above are met, the potential participant will receive a 15 gram challenge dose of ascorbate via intravenous infusion. This is the final screening procedure
| 1
|
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NCT00929006
|
,19:35:chronic_disease
|
For girls without hyperandrogenism: serum (calculated) free testosterone concentration within the Tanner stage-specific reference range and the absence of hirsutism
| 1
|
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NCT02606045
|
20:38:treatment,40:54:treatment,56:63:treatment,65:72:treatment,76:82:treatment
|
Concomitant use of antiplatelet drugs, anticoagulants, dextran, aspirin or NSAIDs
| 1
|
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NCT02277613
|
39:66:chronic_disease
|
Mechanical complications of the index acute myocardial infarction
| 1
|
[
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NCT02324387
|
1:18:chronic_disease
|
nodal involvement (N0 - N3)
| 1
|
[
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[
2,
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0
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NCT02872857
|
1:14:chronic_disease,,
|
Renal disease as defined by creatinine clearance less than 9 milliliters/min
| 1
|
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NCT02129348
|
22:29:treatment,76:97:chronic_disease,145:160:chronic_disease
|
Contraindications to lithium in this study include: resting tremor causing functional impairment, history of falls in the last month, untreated thyroid disease or any abnormal thyroid function test (T3, T4, or TSH)
| 1
|
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NCT02261519
|
5:23:chronic_disease,,,,
|
Any movement disorders with a total score higher than 6 on SAS scale, or more than 2 on any items of the AIMS scale
| 1
|
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NCT01993719
|
,,120:129:treatment
|
Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the treatment on the fetus or infant
| 1
|
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NCT01568918
|
1:19:treatment
|
Lumbar Laminectomy
| 1
|
[
"Lumbar",
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] |
[
1,
1
] |
NCT01553214
|
12:34:chronic_disease
|
History of coronary heart disease
| 1
|
[
"History",
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"heart",
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] |
[
0,
0,
2,
2,
2
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NCT02515773
|
1:8:chronic_disease,1:10:chronic_disease,12:22:chronic_disease,56:65:chronic_disease,67:112:chronic_disease,114:134:chronic_disease,194:207:chronic_disease
|
bipolar I, bipolar II, unspecified bipolar and related disorders, Disruptive Mood Dysregulation Disorder (DMDD), cyclothymic disorder, other specified bipolar and related disorders, as well as mood disorder not otherwise specified (if diagnosed in the past as per DSM-IV)
| 1
|
[
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NCT00540761
|
1:25:chronic_disease
|
congestive heart failure
| 1
|
[
"congestive",
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] |
[
2,
2,
2
] |
NCT02050347
|
,,141:153:treatment
|
Sexually active patients must be willing to utilize one of the more effective birth control methods during the study and for 6 months after ATL infusion
| 1
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NCT02091141
|
82:90:allergy_name,94:114:allergy_name,118:133:allergy_name
|
History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins
| 1
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NCT00472329
|
18:21:chronic_disease
|
Patients who are HIV positive
| 1
|
[
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[
0,
0,
0,
2,
0
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NCT02236013
|
13:24:chronic_disease,29:43:chronic_disease
|
Subject has hypokalemia and hypomagnesemia at Screening (defined as values below institutional lower limit of normal [LLN])
| 1
|
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NCT02143726
|
15:38:treatment,,
|
have received prior radiation therapy to index lesions ≥ 28 days prior to registration on this protocol if there has been documented progression by RECIST criteria
| 1
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NCT00678145
|
1:10:chronic_disease
|
Hepatitis
| 1
|
[
"Hepatitis"
] |
[
2
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NCT02975986
|
1:9:chronic_disease
|
diabetes status
| 1
|
[
"diabetes",
"status"
] |
[
2,
0
] |
NCT01859819
|
49:74:chronic_disease,94:118:chronic_disease,206:213:treatment
|
These patients are excluded due to the expected intense immunosuppression, increased risk of opportunistic infections, and higher expected septic death rate in this subgroup of patients with this proposed therapy
| 1
|
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NCT02155699
|
8:26:chronic_disease
|
have a psychotic disorder (at study entry) and/or have exhibited serious self-harm behaviors
| 1
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NCT02139436
|
7:27:chronic_disease
|
other neurological disease
| 1
|
[
"other",
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"disease"
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[
0,
2,
2
] |
NCT01941316
|
31:41:chronic_disease,,,
|
Must not have any significant neuropathy (Grades 3-4, or Grade 2 with pain) within 14 days prior to enrollment
| 1
|
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NCT02427841
|
102:110:chronic_disease
|
History of allergic reactions attributed to compounds of similar chemical or biologic composition to ABRAXANE or other agents used in the study
| 1
|
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NCT02429830
|
59:68:treatment
|
Subject has been informed of the study procedures and the treatment and has signed an informed consent form
| 1
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NCT02826681
|
8:41:chronic_disease
|
Active acute or known chronic infections
| 1
|
[
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[
0,
2,
2,
2,
2,
2
] |
NCT02423863
|
69:84:chronic_disease
|
While animal reproductive studies have been negative, the simulated viral infection and anti-proliferative activity of this experimental drug may theoretically affect the developing fetus or nursing infant
| 1
|
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NCT02477839
|
,,80:84:treatment
|
Subject is on a stable (concurrently or sequentially) dosage regimen of 1 to 3 AEDs
| 1
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NCT02535312
|
1:25:treatment
|
anti-seizure medications are eligible to participate
| 1
|
[
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[
1,
1,
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0,
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NCT02148796
|
1:38:chronic_disease
|
primary or secondary immunodeficiency
| 1
|
[
"primary",
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"secondary",
"immunodeficiency"
] |
[
2,
2,
2,
2
] |
NCT02030990
|
13:21:chronic_disease,,
|
Evidence of glaucoma or an intraocular pressure greater than 22 mm Hg at baseline
| 1
|
[
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0,
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0,
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0,
0,
0
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NCT03100370
|
4:34:chronic_disease
|
No neuropsychiatric comorbidities
| 1
|
[
"No",
"neuropsychiatric",
"comorbidities"
] |
[
0,
2,
2
] |
NCT01964859
|
130:151:chronic_disease,153:170:cancer,172:191:chronic_disease,200:203:chronic_disease,205:214:chronic_disease,216:227:chronic_disease,229:240:chronic_disease
|
Having a significant medical history that the investigator feels is not safe for study participation (for example, some forms of autoimmune conditions, metastatic cancer, infectious diseases such as HIV, HTLV I/II, Hepatitis B, Hepatitis C)
| 1
|
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NCT00919503
|
19:36:treatment,
|
Receiving another experimental drug within 4 weeks of initiation of conditioning (day -6) unless approved by the PI
| 1
|
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] |
NCT02498613
|
,,53:61:treatment,66:75:treatment,248:257:treatment
|
Pregnant women are excluded from this study because olaparib and cediranib have the potential for teratogenic or abortifacient effects; due to the fact that there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with olaparib and cediranib, breastfeeding should be discontinued if the mother is treated with cediranib and olaparib
| 1
|
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NCT02957149
|
32:56:cancer
|
Metastatic or locally advanced prostatic adenocarcinoma on preoperative evaluation
| 1
|
[
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"adenocarcinoma",
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[
0,
0,
0,
0,
3,
3,
0,
0,
0
] |
NCT03181516
|
8:16:chronic_disease,
|
Active diarrhea (diarrhea is defined in this study as three or more loose stools per day for two consecutive days)
| 1
|
[
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"stools",
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0
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NCT02195232
|
29:50:chronic_disease,
|
Prior history of documented venous thromboembolic event within the last 2 years
| 1
|
[
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"thromboembolic",
"event",
"within",
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0,
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0
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NCT02266745
|
10:20:chronic_disease
|
Previous malignancy
| 1
|
[
"Previous",
"malignancy"
] |
[
0,
2
] |
NCT02738749
|
9:46:chronic_disease
|
have an acute or chronic inflammatory illness that might alter white cell mRNA expression
| 1
|
[
"have",
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0,
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2,
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0,
0,
0,
0,
0,
0
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NCT01419561
|
37:62:cancer,67:84:chronic_disease,105:127:chronic_disease
|
Body cavity effusions not caused by primary effusion lymphoma nor chylous effusions directly related to lymphatic infiltration by KS
| 1
|
[
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"effusions",
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NCT02106312
|
1:7:treatment,15:18:chronic_disease,34:70:treatment,96:111:cancer,123:145:cancer,233:248:cancer,310:315:treatment,363:384:treatment
|
Biopsy proven MLS (including the reciprocal chromosomal translocation t(12;16)(q13;p11); A the primary sarcoma in case of non-metastatic disease for management is with curative intent (regimen to be chosen = 18 x 2 GY) B in case of oligometastatic patients, the metastasis may also be irradiated to a dose of 36 GY in order to postpone the time interval to next systemic chemotherapy. These patients are usually not operated upon and the total dose may also be reached in 12 times 3 Gy, for convenience purposes (see paragraph 10 for radiobiological considerations)
| 1
|
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1,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03042897
|
30:42:treatment
|
Is a candidate for immediate hysterectomy, following evaluation by a physician
| 1
|
[
"Is",
"a",
"candidate",
"for",
"immediate",
"hysterectomy",
",",
"following",
"evaluation",
"by",
"a",
"physician"
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[
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
NCT02460653
|
19:43:chronic_disease
|
Patients who have congenital heart defects
| 1
|
[
"Patients",
"who",
"have",
"congenital",
"heart",
"defects"
] |
[
0,
0,
0,
2,
2,
2
] |
NCT02261857
|
19:31:treatment
|
On-going need for CPAP therapy based on polysomnography
| 1
|
[
"On-going",
"need",
"for",
"CPAP",
"therapy",
"based",
"on",
"polysomnography"
] |
[
0,
0,
0,
1,
1,
0,
0,
0
] |
NCT02544880
|
52:57:cancer
|
Surgically resectable, recurrent or second primary HNSCC
| 1
|
[
"Surgically",
"resectable",
",",
"recurrent",
"or",
"second",
"primary",
"HNSCC"
] |
[
0,
0,
0,
0,
0,
0,
0,
3
] |
NCT02091999
|
1:17:chronic_disease,21:34:chronic_disease,41:50:chronic_disease
|
Active infection or corneal ulcer (e.g. keratitis)
| 1
|
[
"Active",
"infection",
"or",
"corneal",
"ulcer",
"(",
"e.g",
".",
"keratitis",
")"
] |
[
2,
2,
0,
2,
2,
0,
0,
0,
2,
0
] |
NCT02512926
|
,,53:72:treatment
|
Pulse Oximetry measurement ≥ 95% saturation without supplemental oxygen
| 1
|
[
"Pulse",
"Oximetry",
"measurement",
"≥",
"95",
"%",
"saturation",
"without",
"supplemental",
"oxygen"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02419560
|
11:19:cancer
|
Known CNS lymphoma
| 1
|
[
"Known",
"CNS",
"lymphoma"
] |
[
0,
0,
3
] |
NCT02915744
|
7:17:cancer,30:43:cancer,,114:127:treatment
|
Prior malignancy (other than breast cancer) unless diagnosed and definitively treated more than 5 years prior to randomization
| 1
|
[
"Prior",
"malignancy",
"(",
"other",
"than",
"breast",
"cancer",
")",
"unless",
"diagnosed",
"and",
"definitively",
"treated",
"more",
"than",
"5",
"years",
"prior",
"to",
"randomization"
] |
[
0,
3,
0,
0,
0,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02187848
|
1:27:chronic_disease
|
Cardiac conduction defects
| 1
|
[
"Cardiac",
"conduction",
"defects"
] |
[
2,
2,
2
] |
NCT02003222
|
1:20:treatment
|
MAINTENANCE THERAPY
| 1
|
[
"MAINTENANCE",
"THERAPY"
] |
[
1,
1
] |
NCT02225548
|
31:40:treatment,45:65:chronic_disease,94:109:treatment,111:125:treatment,127:147:treatment,149:159:treatment,161:183:treatment,185:189:treatment,195:242:treatment
|
unwilling to cease use of any treatment for erectile dysfunction during the study, including oral medication, vacuum devices, constrictive devices, injections, urethral suppositories, gels, any over-the-counter or nonprescription medications, and products purchased via the internet
| 1
|
[
"unwilling",
"to",
"cease",
"use",
"of",
"any",
"treatment",
"for",
"erectile",
"dysfunction",
"during",
"the",
"study",
",",
"including",
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"medication",
",",
"vacuum",
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",",
"constrictive",
"devices",
",",
"injections",
",",
"urethral",
"suppositories",
",",
"gels",
",",
"any",
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"or",
"nonprescription",
"medications",
",",
"and",
"products",
"purchased",
"via",
"the",
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[
0,
0,
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0,
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1,
0,
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02536794
|
1:35:chronic_disease
|
human immunodeficiency virus (HIV)
| 1
|
[
"human",
"immunodeficiency",
"virus",
"(",
"HIV",
")"
] |
[
2,
2,
2,
2,
0,
0
] |
NCT02469519
|
19:34:treatment
|
Already receiving corticosteroids for another condition
| 1
|
[
"Already",
"receiving",
"corticosteroids",
"for",
"another",
"condition"
] |
[
0,
0,
1,
0,
0,
0
] |
NCT02081404
|
,,,22:46:chronic_disease
|
NYHA class III or IV congestive heart failure
| 1
|
[
"NYHA",
"class",
"III",
"or",
"IV",
"congestive",
"heart",
"failure"
] |
[
0,
0,
0,
0,
0,
2,
2,
2
] |
NCT02524275
|
23:67:cancer,143:150:treatment,158:175:treatment,208:226:cancer
|
Histologically proven squamous cell carcinoma of the head and neck with measurable disease that is either recurrent after attempted cure with surgery and/or radiation therapy or newly diagnosed disease with distant metastases or incurable at diagnosis
| 1
|
[
"Histologically",
"proven",
"squamous",
"cell",
"carcinoma",
"of",
"the",
"head",
"and",
"neck",
"with",
"measurable",
"disease",
"that",
"is",
"either",
"recurrent",
"after",
"attempted",
"cure",
"with",
"surgery",
"and/or",
"radiation",
"therapy",
"or",
"newly",
"diagnosed",
"disease",
"with",
"distant",
"metastases",
"or",
"incurable",
"at",
"diagnosis"
] |
[
0,
0,
3,
3,
3,
3,
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1,
0,
1,
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0,
0,
0,
0,
3,
3,
0,
0,
0,
0
] |
NCT02152956
|
20:37:chronic_disease
|
resolved childhood atopic dermatitis
| 1
|
[
"resolved",
"childhood",
"atopic",
"dermatitis"
] |
[
0,
0,
2,
2
] |
NCT02320292
|
19:31:treatment
|
No indication for chemotherapy
| 1
|
[
"No",
"indication",
"for",
"chemotherapy"
] |
[
0,
0,
0,
1
] |
NCT03153982
|
1:15:cancer
|
Primary tumors of any head and neck (oral cavity, oropharynx, hypopharynx, or larynx) site will be included
| 1
|
[
"Primary",
"tumors",
"of",
"any",
"head",
"and",
"neck",
"(",
"oral",
"cavity",
",",
"oropharynx",
",",
"hypopharynx",
",",
"or",
"larynx",
")",
"site",
"will",
"be",
"included"
] |
[
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02451423
|
82:90:allergy_name,94:114:allergy_name,118:133:allergy_name
|
History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins
| 1
|
[
"History",
"of",
"severe",
"allergic",
",",
"anaphylactic",
",",
"or",
"other",
"hypersensitivity",
"reactions",
"to",
"chimeric",
"or",
"humanized",
"antibodies",
"or",
"fusion",
"proteins"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4,
0,
4,
4,
0,
4,
4
] |
NCT02574728
|
1:23:chronic_disease
|
Uncontrolled infection
| 1
|
[
"Uncontrolled",
"infection"
] |
[
2,
2
] |
NCT01737502
|
41:52:cancer,54:62:cancer,64:90:cancer,94:116:cancer
|
Histologic or cytologic confirmation of lung cancer (squamous, ras-mutated adenocarcinoma or small cell lung cancer)
| 1
|
[
"Histologic",
"or",
"cytologic",
"confirmation",
"of",
"lung",
"cancer",
"(",
"squamous",
",",
"ras-mutated",
"adenocarcinoma",
"or",
"small",
"cell",
"lung",
"cancer",
")"
] |
[
0,
0,
0,
0,
0,
3,
3,
0,
3,
0,
3,
3,
0,
3,
3,
3,
3,
0
] |
NCT02519348
|
58:67:treatment,73:82:treatment,103:106:treatment
|
Have either progressed on, are intolerant to, or refused treatment with sorafenib or another approved TKI
| 1
|
[
"Have",
"either",
"progressed",
"on",
",",
"are",
"intolerant",
"to",
",",
"or",
"refused",
"treatment",
"with",
"sorafenib",
"or",
"another",
"approved",
"TKI"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
0,
0,
1
] |
NCT02152956
|
7:44:cancer
|
Known central nervous system (CNS) leukemia
| 1
|
[
"Known",
"central",
"nervous",
"system",
"(",
"CNS",
")",
"leukemia"
] |
[
0,
3,
3,
3,
3,
3,
0,
0
] |
NCT02565407
|
25:49:treatment,56:75:treatment,84:109:treatment
|
Is currently taking any pro-epileptic medication (e.g. epileptogenic drugs such as tricyclic antidepressants)
| 1
|
[
"Is",
"currently",
"taking",
"any",
"pro-epileptic",
"medication",
"(",
"e.g",
".",
"epileptogenic",
"drugs",
"such",
"as",
"tricyclic",
"antidepressants",
")"
] |
[
0,
0,
0,
0,
1,
1,
0,
0,
0,
1,
1,
0,
0,
1,
1,
0
] |
NCT00368355
|
22:37:chronic_disease,,,,
|
Patients with severe hepatic disease (direct bilirubin greater than 3 ug/dl or SGPT (serum glutamic-pyruvic transaminase) greater than 500 ug/dl)
| 1
|
[
"Patients",
"with",
"severe",
"hepatic",
"disease",
"(",
"direct",
"bilirubin",
"greater",
"than",
"3",
"ug/dl",
"or",
"SGPT",
"(",
"serum",
"glutamic-pyruvic",
"transaminase",
")",
"greater",
"than",
"500",
"ug/dl",
")"
] |
[
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02656706
|
,,122:131:treatment
|
must agree to use adequate barrier birth control measures during the course of the study and up to 2 months after end of treatment
| 1
|
[
"must",
"agree",
"to",
"use",
"adequate",
"barrier",
"birth",
"control",
"measures",
"during",
"the",
"course",
"of",
"the",
"study",
"and",
"up",
"to",
"2",
"months",
"after",
"end",
"of",
"treatment"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT03159936
|
1:17:treatment,
|
Systemic therapy is allowed if on a stable dose and using for at least 3 months -background therapies outlined in Protocol
| 1
|
[
"Systemic",
"therapy",
"is",
"allowed",
"if",
"on",
"a",
"stable",
"dose",
"and",
"using",
"for",
"at",
"least",
"3",
"months",
"-background",
"therapies",
"outlined",
"in",
"Protocol"
] |
[
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02360579
|
1:44:treatment
|
Intrauterine hormone-releasing system (IUS)
| 1
|
[
"Intrauterine",
"hormone-releasing",
"system",
"(",
"IUS",
")"
] |
[
1,
1,
1,
1,
0,
0
] |
NCT03023449
|
16:36:chronic_disease
|
History of any neurological disease
| 1
|
[
"History",
"of",
"any",
"neurological",
"disease"
] |
[
0,
0,
0,
2,
2
] |
NCT02140554
|
26:66:chronic_disease,68:73:chronic_disease,78:83:chronic_disease,86:109:chronic_disease,114:131:chronic_disease
|
Positive for presence of human immunodeficiency virus type 1 or 2 (HIV-1 and HIV-2), hepatitis B virus (HBV), or hepatitis C (HCV)
| 1
|
[
"Positive",
"for",
"presence",
"of",
"human",
"immunodeficiency",
"virus",
"type",
"1",
"or",
"2",
"(",
"HIV-1",
"and",
"HIV-2",
")",
",",
"hepatitis",
"B",
"virus",
"(",
"HBV",
")",
",",
"or",
"hepatitis",
"C",
"(",
"HCV",
")"
] |
[
0,
0,
0,
0,
2,
2,
2,
2,
2,
2,
2,
0,
2,
0,
2,
0,
0,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03181126
|
,73:85:treatment
|
Refractory is defined as persistent disease after at least 2 courses of chemotherapy
| 1
|
[
"Refractory",
"is",
"defined",
"as",
"persistent",
"disease",
"after",
"at",
"least",
"2",
"courses",
"of",
"chemotherapy"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02013492
|
35:63:treatment
|
Patients may not be receiving any other investigational agents
| 1
|
[
"Patients",
"may",
"not",
"be",
"receiving",
"any",
"other",
"investigational",
"agents"
] |
[
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02622984
|
14:31:treatment
|
Currently in alcohol treatment
| 1
|
[
"Currently",
"in",
"alcohol",
"treatment"
] |
[
0,
0,
1,
1
] |
NCT03141359
|
16:26:cancer,
|
Prior invasive malignancy unless disease free for a minimum of 3 years from enrollment
| 1
|
[
"Prior",
"invasive",
"malignancy",
"unless",
"disease",
"free",
"for",
"a",
"minimum",
"of",
"3",
"years",
"from",
"enrollment"
] |
[
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
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