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NCT02525692
|
1:32:treatment,34:68:treatment,72:85:treatment,102:108:treatment,176:181:cancer,260:299:treatment,320:329:treatment
|
Prior stereotactic radiotherapy, convection enhanced delivery (CED) or brachytherapy must have had a biopsy to confirm radiographic progression is consistent with progressive tumor and not treatment-related necrosis. If the recurrent lesion is outside of any prior high-dose radiation target volume or distant from the prior CED or brachytherapy site, subjects will be considered eligible
| 1
|
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NCT02298491
|
32:43:chronic_disease
|
A highly probable diagnosis of sarcoidosis, as determined using the World Association for Sarcoidosis and Other Granulomatous Disorders (WASOG) Sarcoidosis Organ Assessment Instrument (Judson et al., 2014), with involvement not limited to the central nervous system
| 1
|
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NCT02321501
|
23:47:chronic_disease,,,
|
history of documented congestive heart failure (New York Heart Association functional classification III-IV)
| 1
|
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NCT00338377
|
9:20:treatment,24:44:treatment,,85:108:treatment
|
Has had prior B-RAF or MEK targeted therapy within 7 days prior to the start of the lymphodepletion regimen (Cohort A and Cohort B)
| 1
|
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NCT01639508
|
1:17:chronic_disease,28:46:treatment,,87:102:treatment
|
active infection requiring systemic treatment within 28 days before the first dose of study treatment
| 1
|
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NCT02187848
|
1:32:treatment
|
Prior therapy targeting CEACAM5
| 1
|
[
"Prior",
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[
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NCT02553941
|
1:64:treatment
|
Prior treatment with a Bruton's tyrosine kinase (BTK) inhibitor
| 1
|
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NCT02484404
|
28:47:chronic_disease,58:65:treatment,93:117:chronic_disease
|
Patients with a history of auto-immune disease requiring steroid maintenance, or history of primary immunodeficiency are not eligible
| 1
|
[
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NCT02724540
|
1:6:cancer
|
Tumor burden dominant in the liver
| 1
|
[
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NCT02501954
|
15:43:cancer
|
Patients with recurrent endometrial cancer
| 1
|
[
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"cancer"
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0,
0,
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3,
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NCT02938559
|
14:45:chronic_disease
|
Diagnosis of major depressive disorder (MDD), first episode, recurrent or chronic, according to DSM-5
| 1
|
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NCT01690468
|
20:38:cancer
|
platinum-resistant epithelial ovarian
| 1
|
[
"platinum-resistant",
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[
0,
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NCT02446093
|
7:39:treatment
|
other systemic immunosuppressive drugs
| 1
|
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"drugs"
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[
0,
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] |
NCT02715583
|
1:30:treatment,
|
Systemic radioisotope therapy within 24 weeks prior to study enrollment
| 1
|
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NCT02441062
|
,,103:126:treatment
|
≥60 years old,or of childbearing potential for whom a pregnancy test (with the results known prior to investigational product administration) is negative
| 1
|
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NCT01626079
|
1:24:chronic_disease,35:44:treatment,56:83:treatment
|
Hemodynamic instability requiring inotropic support or mechanical heart assistance
| 1
|
[
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NCT02272218
|
72:96:chronic_disease,105:116:chronic_disease,118:125:chronic_disease,129:144:chronic_disease,146:156:cancer,160:175:chronic_disease,177:203:chronic_disease,211:220:chronic_disease,222:242:chronic_disease,282:299:treatment,304:321:chronic_disease
|
comorbidities that would make lap band surgery contraindicated (severe cardiopulmonary diseases, severe esophagitis, stomach or duodenal ulcers, esophageal or gastric varices, inflammatory bowel disease, liver cirrhosis, chronic pancreatitis, alcohol or drug addiction, on chronic steroid treatment, or active infections)
| 1
|
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NCT02059239
|
26:29:chronic_disease
|
Known to be positive for HIV
| 1
|
[
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[
0,
0,
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2
] |
NCT02332369
|
1:10:chronic_disease
|
Amblyopia
| 1
|
[
"Amblyopia"
] |
[
2
] |
NCT03154476
|
61:93:treatment
|
All adult Fontan patients who have no contraindications for magnetic resonance imaging (MRI) will be eligible for the study
| 1
|
[
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NCT02354547
|
51:61:cancer
|
Patients must have had histologic verification of malignancy at original diagnosis or relapse
| 1
|
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NCT02910700
|
98:116:chronic_disease
|
inhaled or topical steroids and adrenal replacement doses are permitted in the absence of active autoimmune disease
| 1
|
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NCT03171493
|
14:54:cancer
|
Diagnosis of Urothelial carcinoma (UC) of the bladder, with histologic confirmation of primary UC pathology
| 1
|
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NCT02128906
|
24:36:treatment
|
breast feeding because chemotherapy
| 1
|
[
"breast",
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[
0,
0,
0,
1
] |
NCT02876302
|
58:71:cancer
|
Participants must have histologically confirmed invasive breast cancer
| 1
|
[
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3,
3
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NCT00719888
|
1:13:treatment,14:35:cancer,40:54:cancer,,92:108:treatment
|
Chemotherapy refractory large cell and high grade NHL (i.e., progressive disease after > 2 salvage regimens)
| 1
|
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NCT02408861
|
1:4:chronic_disease,,
|
HIV viral load should be well suppressed, defined as below the limit of detection of the local assay or below 75 copies/mL by Food and Drug Administration (FDA)-approved assays, within 4 weeks prior to registration
| 1
|
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NCT02553642
|
1:23:treatment
|
Prior therapy with BCG
| 1
|
[
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[
1,
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1,
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] |
NCT01614990
|
38:50:treatment
|
subjects may otherwise be undergoing chemotherapy
| 1
|
[
"subjects",
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[
0,
0,
0,
0,
0,
1
] |
NCT02843165
|
,,,82:101:treatment
|
Patient is a pregnant woman (pregnant women are excluded from this study because radiation treatment has known potential for teratogenic or abortifacient effects)
| 1
|
[
"Patient",
"is",
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"women",
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NCT02588326
|
1:12:chronic_disease
|
common cold
| 1
|
[
"common",
"cold"
] |
[
2,
2
] |
NCT02939183
|
14:24:treatment,
|
received the transplant within 6 months prior to study day 1
| 1
|
[
"received",
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"months",
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[
0,
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] |
NCT02496611
|
12:27:chronic_disease
|
History of suicide attempt
| 1
|
[
"History",
"of",
"suicide",
"attempt"
] |
[
0,
0,
2,
2
] |
NCT02350764
|
14:24:cancer
|
Other active malignancy requiring concurrent intervention
| 1
|
[
"Other",
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"malignancy",
"requiring",
"concurrent",
"intervention"
] |
[
0,
0,
3,
0,
0,
0
] |
NCT02953392
|
4:19:chronic_disease
|
No apical disorder/inflammation at the area of the implant site
| 1
|
[
"No",
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"disorder/inflammation",
"at",
"the",
"area",
"of",
"the",
"implant",
"site"
] |
[
0,
2,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02115685
|
1:18:chronic_disease
|
unhealed decubiti
| 1
|
[
"unhealed",
"decubiti"
] |
[
2,
2
] |
NCT01261728
|
31:40:treatment
|
Supportive care trials or non-treatment trials, e.g. QOL
| 1
|
[
"Supportive",
"care",
"trials",
"or",
"non-treatment",
"trials",
",",
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"QOL"
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0,
0,
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT02924441
|
30:43:cancer
|
Must not have had history of breast cancer
| 1
|
[
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"history",
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"breast",
"cancer"
] |
[
0,
0,
0,
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0,
0,
3,
3
] |
NCT01061515
|
105:117:treatment
|
must undergo a peritoneal scan documenting at least one working intraperitoneal port prior to receiving chemotherapy
| 1
|
[
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NCT02544373
|
13:40:chronic_disease,102:111:chronic_disease,115:131:chronic_disease
|
Concomitant systemic autoimmune disease with secondary central nervous system involvement (including CNS lupus or neurosarcoidosis)
| 1
|
[
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"systemic",
"autoimmune",
"disease",
"with",
"secondary",
"central",
"nervous",
"system",
"involvement",
"(",
"including",
"CNS",
"lupus",
"or",
"neurosarcoidosis",
")"
] |
[
0,
2,
2,
2,
0,
0,
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0,
0,
0,
0,
0,
2,
2,
0,
2,
0
] |
NCT01883076
|
20:53:treatment
|
undergoing planned Stage II palliative Glenn surgery
| 1
|
[
"undergoing",
"planned",
"Stage",
"II",
"palliative",
"Glenn",
"surgery"
] |
[
0,
0,
1,
1,
1,
1,
1
] |
NCT02352025
|
54:67:cancer
|
Any prior treatment for the current, newly diagnosed breast cancer
| 1
|
[
"Any",
"prior",
"treatment",
"for",
"the",
"current",
",",
"newly",
"diagnosed",
"breast",
"cancer"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3
] |
NCT02857283
|
1:22:chronic_disease
|
chronic renal disease
| 1
|
[
"chronic",
"renal",
"disease"
] |
[
2,
2,
2
] |
NCT01505569
|
14:19:cancer
|
Arm A: Solid Tumor
| 1
|
[
"Arm",
"A",
":",
"Solid",
"Tumor"
] |
[
0,
0,
0,
0,
3
] |
NCT00670358
|
10:27:cancer,46:70:cancer,64:70:cancer
|
No other active malignancy, except localized nonmelanotic skin cancer or any cancer that, in the judgment of the investigator, has been treated with curative intent and will not interfere with the study treatment plan and response assessment
| 1
|
[
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NCT01974609
|
36:65:treatment
|
All patients undergoing elective a primary carpal tunnel release
| 1
|
[
"All",
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"undergoing",
"elective",
"a",
"primary",
"carpal",
"tunnel",
"release"
] |
[
0,
0,
0,
0,
0,
1,
1,
1,
1
] |
NCT02203695
|
24:46:chronic_disease
|
Clinically significant cardiovascular disease
| 1
|
[
"Clinically",
"significant",
"cardiovascular",
"disease"
] |
[
0,
0,
2,
2
] |
NCT01954576
|
9:15:treatment,19:28:treatment,42:47:cancer,175:192:treatment
|
Planned biopsy or resection of recurrent tumor for therapeutic and/or diagnostic purpose, and with adequate bone marrow, hepatic, cardiac, and renal function to undergo this planned procedure
| 1
|
[
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"biopsy",
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"resection",
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"recurrent",
"tumor",
"for",
"therapeutic",
"and/or",
"diagnostic",
"purpose",
",",
"and",
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"bone",
"marrow",
",",
"hepatic",
",",
"cardiac",
",",
"and",
"renal",
"function",
"to",
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] |
NCT02266004
|
8:18:treatment
|
Stable medication regimen
| 1
|
[
"Stable",
"medication",
"regimen"
] |
[
0,
1,
0
] |
NCT02690116
|
16:29:cancer,,
|
Diagnosed with breast cancer, stage 0-III
| 1
|
[
"Diagnosed",
"with",
"breast",
"cancer",
",",
"stage",
"0-III"
] |
[
0,
0,
3,
3,
0,
0,
0
] |
NCT02166905
|
40:50:treatment
|
The ability to swallow and retain oral medication
| 1
|
[
"The",
"ability",
"to",
"swallow",
"and",
"retain",
"oral",
"medication"
] |
[
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02437110
|
10:25:chronic_disease,35:50:chronic_disease,54:91:chronic_disease,97:122:chronic_disease,132:143:chronic_disease,147:159:chronic_disease,173:183:cancer
|
Unstable medical disease (such as unstable angina or chronic obstructive pulmonary disease), or active infectious disease (such as Hepatitis C or tuberculosis), or current malignancy
| 1
|
[
"Unstable",
"medical",
"disease",
"(",
"such",
"as",
"unstable",
"angina",
"or",
"chronic",
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"pulmonary",
"disease",
")",
",",
"or",
"active",
"infectious",
"disease",
"(",
"such",
"as",
"Hepatitis",
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"or",
"tuberculosis",
")",
",",
"or",
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NCT01474889
|
1:63:treatment,
|
Treatment with any anti-diabetic medication other than insulin within 4 weeks of enrollment
| 1
|
[
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"any",
"anti-diabetic",
"medication",
"other",
"than",
"insulin",
"within",
"4",
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[
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1,
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0,
0,
0,
0,
0
] |
NCT02587403
|
21:31:cancer,51:63:treatment,,,164:167:cancer,171:174:cancer
|
Have a known active malignancy present and/or had chemotherapy 12 weeks prior to screening or planned chemotherapy within 12 weeks of enrollment with exception of BCC or SCC
| 1
|
[
"Have",
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"12",
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] |
NCT02227199
|
,35:79:treatment
|
Prior failed (< 5 x 10^6 CD34/kg) peripheral blood stem cell (PBSC) collection
| 1
|
[
"Prior",
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"CD34/kg",
")",
"peripheral",
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0,
0,
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1,
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1,
1,
1,
0,
0
] |
NCT02587962
|
62:99:cancer,157:164:treatment,261:273:cancer
|
Patients must have histologically or cytologically confirmed head and neck squamous cell carcinoma that is locally advanced or metastatic with no available therapy options that are known to provide clinical benefit per institutional standard of care. (various solid tumors cohort: head and neck squamous cell carcinoma groups only)
| 1
|
[
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NCT02085941
|
1:6:cancer
|
Tumor displacement from nerves may be required and will be performed as deemed appropriate to avoid nerve injury
| 1
|
[
"Tumor",
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"nerves",
"may",
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"required",
"and",
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"performed",
"as",
"deemed",
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0,
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0,
0,
0,
0,
0,
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0
] |
NCT01568918
|
1:23:chronic_disease
|
Lumbar Anterior Fusion
| 1
|
[
"Lumbar",
"Anterior",
"Fusion"
] |
[
2,
2,
2
] |
NCT03153319
|
4:22:treatment,
|
no treatment with ERT for ≥1 year
| 1
|
[
"no",
"treatment",
"with",
"ERT",
"for",
"≥1",
"year"
] |
[
0,
1,
1,
1,
0,
0,
0
] |
NCT02920086
|
1:13:treatment
|
Vasopressors
| 1
|
[
"Vasopressors"
] |
[
1
] |
NCT02366611
|
41:45:treatment,56:73:chronic_disease,75:90:treatment,92:119:treatment,121:137:chronic_disease,139:159:chronic_disease
|
Any condition that would prevent use of tDCS including skull abnormality, implanted metal, implanted electronic device, seizure disorder, neurologic condition
| 1
|
[
"Any",
"condition",
"that",
"would",
"prevent",
"use",
"of",
"tDCS",
"including",
"skull",
"abnormality",
",",
"implanted",
"metal",
",",
"implanted",
"electronic",
"device",
",",
"seizure",
"disorder",
",",
"neurologic",
"condition"
] |
[
0,
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2,
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2,
2
] |
NCT01306019
|
48:54:treatment,56:67:chronic_disease,76:89:treatment,91:103:treatment,169:178:chronic_disease
|
Isolation of a bacteria, fungus, or virus from biopsy, skin lesion, blood, nasal washing, bronchoscopy, cerebrospinal fluid or stool likely to be an etiologic agent of infection
| 1
|
[
"Isolation",
"of",
"a",
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",",
"fungus",
",",
"or",
"virus",
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",",
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"blood",
",",
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",",
"bronchoscopy",
",",
"cerebrospinal",
"fluid",
"or",
"stool",
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"an",
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2
] |
NCT02496611
|
1:22:chronic_disease
|
Neurological disorder
| 1
|
[
"Neurological",
"disorder"
] |
[
2,
2
] |
NCT02914834
|
1:23:chronic_disease
|
autoimmune dysfunction
| 1
|
[
"autoimmune",
"dysfunction"
] |
[
2,
2
] |
NCT03158519
|
27:37:cancer
|
Diagnosis of other active malignancy
| 1
|
[
"Diagnosis",
"of",
"other",
"active",
"malignancy"
] |
[
0,
0,
0,
0,
3
] |
NCT01990209
|
36:55:treatment,87:96:treatment,100:103:treatment
|
LHRH agonists maybe used to render ovarian suppression with post-menopausal ranges of estradiol or FSH per institutional guidelines
| 1
|
[
"LHRH",
"agonists",
"maybe",
"used",
"to",
"render",
"ovarian",
"suppression",
"with",
"post-menopausal",
"ranges",
"of",
"estradiol",
"or",
"FSH",
"per",
"institutional",
"guidelines"
] |
[
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
1,
0,
1,
0,
0,
0
] |
NCT01925573
|
58:70:treatment
|
6 weeks since the completion of a nitrosourea-containing chemotherapy regimen
| 1
|
[
"6",
"weeks",
"since",
"the",
"completion",
"of",
"a",
"nitrosourea-containing",
"chemotherapy",
"regimen"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
1,
0
] |
NCT02315612
|
43:73:treatment
|
There is no time restriction in regard to prior intrathecal chemotherapy provided there is complete recovery from any acute toxic effects
| 1
|
[
"There",
"is",
"no",
"time",
"restriction",
"in",
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"to",
"prior",
"intrathecal",
"chemotherapy",
"provided",
"there",
"is",
"complete",
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] |
[
0,
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0,
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0,
0,
0,
0
] |
NCT02562716
|
20:36:treatment,
|
Patients must have surgical consult to verify patient is a surgical candidate within 21 days prior to registration
| 1
|
[
"Patients",
"must",
"have",
"surgical",
"consult",
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"verify",
"patient",
"is",
"a",
"surgical",
"candidate",
"within",
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"prior",
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[
0,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03158116
|
12:24:chronic_disease
|
History of tuberculosis
| 1
|
[
"History",
"of",
"tuberculosis"
] |
[
0,
0,
2
] |
NCT02531932
|
43:54:allergy_name
|
Patients with a known hypersensitivity to carboplatin
| 1
|
[
"Patients",
"with",
"a",
"known",
"hypersensitivity",
"to",
"carboplatin"
] |
[
0,
0,
0,
0,
0,
0,
4
] |
NCT02966223
|
51:63:treatment
|
Subjects who have contraindications for receiving Y-90 therapy and any routine procedures and imaging associated with Y-90 therapy
| 1
|
[
"Subjects",
"who",
"have",
"contraindications",
"for",
"receiving",
"Y-90",
"therapy",
"and",
"any",
"routine",
"procedures",
"and",
"imaging",
"associated",
"with",
"Y-90",
"therapy"
] |
[
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02521818
|
12:24:chronic_disease
|
history of pancreatitis
| 1
|
[
"history",
"of",
"pancreatitis"
] |
[
0,
0,
2
] |
NCT02172651
|
27:39:treatment,43:55:treatment,,,84:95:treatment,100:115:treatment
|
Participants who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for bevacizumab) of liver resection
| 1
|
[
"Participants",
"who",
"have",
"had",
"chemotherapy",
"or",
"radiotherapy",
"within",
"4",
"weeks",
"(",
"6",
"weeks",
"for",
"bevacizumab",
")",
"of",
"liver",
"resection"
] |
[
0,
0,
0,
0,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
1,
1
] |
NCT02540330
|
1:24:chronic_disease
|
Impaired renal function
| 1
|
[
"Impaired",
"renal",
"function"
] |
[
2,
2,
2
] |
NCT02509507
|
1:13:cancer
|
Liver tumors must not be estimated to invade approximately more than one-third of the liver
| 1
|
[
"Liver",
"tumors",
"must",
"not",
"be",
"estimated",
"to",
"invade",
"approximately",
"more",
"than",
"one-third",
"of",
"the",
"liver"
] |
[
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02176967
|
,,,51:64:cancer
|
< 12 months (< 365 days) of age at diagnosis with INRG stage L1
| 1
|
[
"<",
"12",
"months",
"(",
"<",
"365",
"days",
")",
"of",
"age",
"at",
"diagnosis",
"with",
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"stage",
"L1"
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[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
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3,
3,
3
] |
NCT02579967
|
,124:136:chronic_disease,138:141:chronic_disease,143:146:chronic_disease,148:152:chronic_disease,154:158:chronic_disease
|
Chronic elevation in the blood (greater than or equal to 2 documented elevations over a period of 6 months or longer) of a latent virus (EBV, CMV, HHV6, HHV8, etc.)
| 1
|
[
"Chronic",
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"greater",
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",",
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",",
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",",
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NCT02099058
|
19:35:cancer,129:140:allergy_name,152:157:allergy_name,159:164:allergy_name,166:171:allergy_name,175:180:allergy_name
|
Subject must have metastatic NSCLC with documented Epidermal Growth Factor Receptor (EGFR) mutation(s) known to be sensitive to osimertinib, including del19, L858R, G719X or L861Q
| 1
|
[
"Subject",
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"G719X",
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4,
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4,
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NCT02495415
|
54:63:treatment
|
patient who tested positive subsequent to their last treatment regimen
| 1
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NCT01976169
|
13:37:chronic_disease,39:63:chronic_disease,65:96:chronic_disease,
|
Symptomatic congestive heart failure, unstable angina pectoris, stroke or myocardial infarction within 3 months
| 1
|
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0,
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NCT02324439
|
30:32:cancer,43:71:cancer,73:98:cancer,102:123:cancer,145:163:treatment,,237:253:treatment
|
Patients with a diagnosis of OC including epithelial ovarian carcinoma, primary peritoneal cancer or fallopian tube cancer who are currently in clinical remission as determined by the PI or co-I and are within 4 months of completion of cancer treatment
| 1
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[
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NCT02309580
|
12:33:chronic_disease,35:50:chronic_disease,55:78:chronic_disease,
|
history of myocardial infarction, unstable angina, or acute coronary syndrome within 6 months prior to enrollment
| 1
|
[
"history",
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",",
"unstable",
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",",
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2,
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2,
2,
0,
0,
0,
0,
0,
0
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NCT02582827
|
12:23:chronic_disease,35:55:chronic_disease,125:134:treatment
|
History of retinopathy, including diabetic retinopathy. All patients must be evaluated by an ophthalmologist prior to study treatment
| 1
|
[
"History",
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",",
"including",
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".",
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0,
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0,
0,
1
] |
NCT01367444
|
29:39:treatment
|
Contraindications to use of anesthesia (local or general, as appropriate)
| 1
|
[
"Contraindications",
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"use",
"of",
"anesthesia",
"(",
"local",
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",",
"as",
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")"
] |
[
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02261519
|
37:42:treatment
|
The subject has previously received NaBen
| 1
|
[
"The",
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"NaBen"
] |
[
0,
0,
0,
0,
0,
1
] |
NCT02135588
|
,40:52:treatment
|
At least 2 days from administration of chemotherapy
| 1
|
[
"At",
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"days",
"from",
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] |
[
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT00630253
|
7:60:cancer,,
|
Early myelodysplastic syndrome, with multilineage dysplasia with < 5% blasts, with or without chromosomal anomalies
| 1
|
[
"Early",
"myelodysplastic",
"syndrome",
",",
"with",
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"with",
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"blasts",
",",
"with",
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"without",
"chromosomal",
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[
0,
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3,
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02340169
|
27:42:allergy_name
|
Allergy or sensitivity to corticosteroids or any drug hypersensitivity or intolerance that would compromise patient safety or study results
| 1
|
[
"Allergy",
"or",
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"to",
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"or",
"any",
"drug",
"hypersensitivity",
"or",
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[
0,
0,
0,
0,
4,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01599559
|
7:10:chronic_disease
|
Known HIV-positive serology
| 1
|
[
"Known",
"HIV-positive",
"serology"
] |
[
0,
2,
0
] |
NCT01967823
|
,,136:145:treatment
|
Patients of both genders must be willing to practice birth control from the time of enrollment on this study and for four months after treatment
| 1
|
[
"Patients",
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"must",
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"the",
"time",
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"enrollment",
"on",
"this",
"study",
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"for",
"four",
"months",
"after",
"treatment"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT01750567
|
12:28:chronic_disease,44:50:chronic_disease,54:58:chronic_disease
|
Ongoing or active infection concerning for sepsis or SIRS
| 1
|
[
"Ongoing",
"or",
"active",
"infection",
"concerning",
"for",
"sepsis",
"or",
"SIRS"
] |
[
0,
0,
2,
2,
0,
0,
2,
0,
2
] |
NCT02849457
|
17:36:treatment,45:55:treatment,59:68:treatment
|
Has received an oral mTOR inhibitor such as everolimus or sirolimus
| 1
|
[
"Has",
"received",
"an",
"oral",
"mTOR",
"inhibitor",
"such",
"as",
"everolimus",
"or",
"sirolimus"
] |
[
0,
0,
0,
1,
1,
1,
0,
0,
1,
0,
1
] |
NCT02232516
|
1:42:cancer
|
Hepatosplenic gamma-delta T-cell lymphoma
| 1
|
[
"Hepatosplenic",
"gamma-delta",
"T-cell",
"lymphoma"
] |
[
3,
3,
3,
3
] |
NCT02479620
|
7:15:chronic_disease
|
Acute thrombus in the target limb
| 1
|
[
"Acute",
"thrombus",
"in",
"the",
"target",
"limb"
] |
[
0,
2,
0,
0,
0,
0
] |
NCT03168776
|
29:69:treatment
|
an acceptable candidate for percutaneous coronary intervention (PCI) with drug-eluting stents
| 1
|
[
"an",
"acceptable",
"candidate",
"for",
"percutaneous",
"coronary",
"intervention",
"(",
"PCI",
")",
"with",
"drug-eluting",
"stents"
] |
[
0,
0,
0,
0,
1,
1,
1,
1,
0,
0,
0,
0,
0
] |
NCT02960555
|
41:58:chronic_disease,,188:194:chronic_disease,196:233:chronic_disease,,323:334:chronic_disease
|
Patients with pre-existing uncontrolled pulmonary disease will be excluded; uncontrolled refers to patients having had at least one hospitalization due to pulmonary disease (for example, asthma, chronic obstructive pulmonary disease) within the 6 months prior to enrollment in the study; patients with previous history of pneumonitis will be excluded
| 1
|
[
"Patients",
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"will",
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0,
0,
0,
0,
0,
0,
2,
0,
0,
0
] |
NCT03007030
|
27:57:allergy_name
|
Known hypersensitivity to brentuximab vedotin components
| 1
|
[
"Known",
"hypersensitivity",
"to",
"brentuximab",
"vedotin",
"components"
] |
[
0,
0,
0,
4,
4,
4
] |
NCT02219711
|
26:48:chronic_disease
|
History of a significant cardiovascular illness
| 1
|
[
"History",
"of",
"a",
"significant",
"cardiovascular",
"illness"
] |
[
0,
0,
0,
0,
2,
2
] |
NCT02474667
|
23:39:chronic_disease
|
Signs and symptoms of volume depletion
| 1
|
[
"Signs",
"and",
"symptoms",
"of",
"volume",
"depletion"
] |
[
0,
0,
0,
0,
2,
2
] |
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