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NCT02522494 | 1:9:chronic_disease | Dementia | {
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NCT02266329 | 26:67:treatment | Current participation in transcranial magnetic stimulation studies | {
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NCT01906385 | 9:28:treatment | Planned stereotactic biopsy as standard of care (ie, for confirmation of disease progression) | {
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NCT02855554 | 1:38:chronic_disease | Hypertrophic cardiomyopathy (group 2) | {
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NCT01306019 | 83:89:cancer | previously diagnosed known genotype of the subject conferring a predisposition to cancer (no DNA or other testing for cancer predisposition genes will be performed as part of the screen for this protocol) | {
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NCT01572480 | 38:60:treatment | Patients who are receiving any other investigational agents | {
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NCT02473250 | 1:17:chronic_disease | blood dyscrasias | {
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NCT02419495 | 73:82:cancer | For the Arm B (paclitaxel) expansion cohort, patients must have ovarian carcinoma | {
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NCT02370693 | 22:31:chronic_disease | No evidence of acute infection | {
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NCT02225548 | 21:38:chronic_disease | Subject with active peptic ulceration | {
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NCT02588027 | 47:58:treatment | Patients with rotator cuff tears that require open repair | {
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NCT02564744 | 51:75:chronic_disease, | For Part 2 and Part 3 of the study, patients with primary refractory DLBCL (defined as progression of disease within 24 weeks after first line of treatment) | {
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NCT02572323 | 26:30:treatment,32:49:treatment,98:115:treatment,125:133:treatment,135:146:treatment,148:156:treatment | active or planned use of rhGH, anabolic steroids (other than replacement doses of testosterone), anti-TNFa therapy or other biologic (tocilizumab, Xelijanz, etc.) | {
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NCT02081404 | 18:55:chronic_disease | oxygen dependent chronic obstructive pulmonary disease | {
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NCT02771626 | 16:45:treatment | Intolerance to prior anti-PD-1/PD-L1 therapy | {
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NCT02089607 | 1:33:chronic_disease,, | Thoracoabdominal aortic aneurysm with a diameter ≥ 5.5 cm or 2 times the normal aortic diameter | {
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NCT03088072 | 1:11:chronic_disease,16:30:chronic_disease,44:64:chronic_disease | AV fistula, or pseudoaneurysm), or serious pericardial effusion) | {
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NCT02314221 | 8:34:chronic_disease | Severe concurrent medical disease, illness or condition | {
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NCT02152956 | 7:22:chronic_disease | prior Grave's disease now euthyroid clinically and by laboratory testing | {
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NCT01943851 | 36:53:chronic_disease,87:98:chronic_disease,100:107:chronic_disease,109:114:chronic_disease,116:131:chronic_disease,159:176:chronic_disease | Evidence of severe or uncontrolled systemic diseases (e.g., unstable or uncompensated respiratory, hepatic, renal, cardiac disease, or clinically significant bleeding episodes) | {
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NCT03170375 | 1:31:chronic_disease | severely uncontrolled diabetes | {
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NCT02589977 | 21:23:chronic_disease | acute decompensated HF | {
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NCT02793921 | 1:17:treatment | wound dehiscence | {
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NCT02460900 | 51:62:allergy_name | Previous allergic reaction or hypersensitivity to Varenicline (by participant report ever in lifetime) | {
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NCT02013154 | 1:10:treatment,16:37:treatment,54:63:treatment, | Treatment with low dose chemotherapy concurrent with radiation within 14 days prior to study entry | {
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NCT02464878 | 12:34:treatment, | Use of any investigational agents within 4 weeks of enrollment | {
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NCT02072356 | 14:37:cancer,67:70:cancer,235:241:cancer,254:259:cancer,276:299:treatment | Diagnosis of intrahepatic malignancy including but not limited to HCC; the histopathology confirmation criterion may be waived in patients with a radiographically identifiable liver mass, known laboratory or clinical risk factors for cancer or elevated tumor markers such as alpha-fetoprotein (AFP) and clinical findings | {
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NCT02520713 | 1:43:cancer | Infantile fibrosarcoma without NTRK fusion | {
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NCT03084640 | 48:62:chronic_disease | Any concurrent uncontrolled illness, including mental illness or substance abuse, which in the opinion of the Investigator | {
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NCT02707471 | ,31:34:chronic_disease | within 12 months of beginning AET | {
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NCT02079857 | 48:71:treatment | Individuals currently receiving other types of complementary therapies | {
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NCT02988960 | 21:32:treatment,60:71:cancer,95:113:treatment,104:113:treatment | Participants in all monotherapy arms must have an advanced solid tumor that has progressed on standard therapies known to provide clinical benefit or the participants are intolerant to such therapies | {
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NCT02471911 | 29:41:cancer,54:70:cancer,,121:131:cancer,133:168:cancer,173:204:cancer,208:214:cancer | Patients who have had prior malignancies (other than B-cell lymphomas) for ≤5 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma in situ of the cervix or breast | {
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NCT02931110 | 19:24:cancer,26:28:cancer,30:33:cancer,35:37:cancer,42:45:cancer,46:49:cancer,, | For subjects with DLBCL, FL, MCL, HL, or CLL/SLL: presence of radiographically measurable lymphadenopathy or extranodal lymphoid malignancy (defined as the presence of ≥1 lesion that measures ≥2.0 cm in the longest dimension [LD] and ≥1.0 cm in the longest perpendicular dimension [LPD] as assessed by computed tomograph... | {
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NCT02064296 | 1:29:chronic_disease,39:52:chronic_disease,60:70:chronic_disease,76:93:chronic_disease, | Severe psychiatric illnesses (current schizophrenia, major depression with suicidal ideation, substance abuse within two years) | {
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NCT02122172 | 19:35:treatment | Inability to take oral medications | {
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NCT01459107 | 119:137:treatment,244:253:treatment,356:387:treatment | No co-existing medical condition which, in the opinion of the study team, could affect the immunomodulatory protocol, surgical procedure, or functional results (see Donor and Recipient Exclusion Criteria below. If the condition is amenable to treatment, the study team must agree that said condition should not significa... | {
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NCT02498262 | 79:94:chronic_disease | Participants will include individuals that have suffered a moderate to severe traumatic brain | {
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NCT03078192 | 27:30:chronic_disease,32:59:chronic_disease,63:75:chronic_disease,77:114:chronic_disease,118:143:chronic_disease,148:153:chronic_disease | Either has a diagnosis of PAH, isolated left heart disease or lung disease (chronic obstructive pulmonary disease or interstitial lung disease) or CTEPH using established clinical criteria | {
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NCT02466750 | 18:31:chronic_disease | Have a confirmed HIV infection (antibody positivity) | {
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NCT01822522 | 1:17:chronic_disease,28:46:treatment,37:46:treatment, | Active infection requiring systemic treatment within 28 days before the first dose of study treatment | {
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NCT02487082 | 1:7:chronic_disease | Asthma | {
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NCT01959698 | 15:20:treatment,35:40:treatment,65:70:treatment,93:116:chronic_disease,117:144:treatment | Patients with HBsAg negative, but HBcAb positive (regardless of HBsAb status) should have a hepatitis B virus (HBV) deoxyribonucleic acid (DNA) testing done and protocol | {
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NCT02243813 | 23:52:treatment | Agree not to take any Pro-re-nata (PRN) medications on the mornings of drug sessions | {
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NCT02474199 | 14:22:treatment | Confirmatory chest CT | {
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NCT02554253 | 9:24:treatment,17:24:treatment,,89:115:treatment,129:157:treatment | Complex cardiac surgery will be defined as surgery involving more than one heart valve, redo-sternotomy procedures, or combined valvular and CABG procedures | {
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NCT02081404 | 21:27:cancer,, | recent diagnosis of cancer with a life-expectancy < 5 years | {
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NCT02109627 | 14:17:chronic_disease,19:30:chronic_disease,34:35:chronic_disease,39:48:chronic_disease | Known active HIV, hepatitis B or C or infection | {
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NCT02159703 | 1:37:chronic_disease | symptomatic congestive heart failure | {
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NCT02133872 | 11:29:treatment | On stable medication regimen | {
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NCT02384954 | 69:78:treatment,102:111:treatment,,301:308:treatment | Anti-CD20 mAb-sensitive disease is defined by a response to a prior rituximab-containing (or another treatment of an anti-CD20 monoclonal antibody) regimen, and relapse more than 6 months from the last administration of rituximab-containing (or another treatment of an anti-CD20 antibody-containing) therapy | {
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NCT01054196 | 1:21:chronic_disease,64:80:chronic_disease,94:118:chronic_disease,120:144:chronic_disease,146:164:chronic_disease,169:206:chronic_disease | Uncontrolled 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 | {
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NCT00737893 | 30:48:chronic_disease | The patient has a history of sickle cell anemia | {
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NCT02235857 | 21:36:allergy_name,38:45:allergy_name,50:64:allergy_name | Hypersensitivity to dextran sulfate, heparin, or ethylene oxide | {
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NCT02513797 | ,,35:58:treatment | LA diameter > 6 cm as measured by computerized tomography and confirmed by the imaging core laboratory | {
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NCT03050801 | 13:31:chronic_disease,35:55:chronic_disease,69:72:chronic_disease,103:109:chronic_disease,111:128:chronic_disease,130:147:chronic_disease,149:162:chronic_disease,166:182:chronic_disease | Any current major neurological or psychiatric disorder unrelated to TBI, such as (but not limited to) stroke, Parkinson disease, Alzheimer disease, schizophrenia or major depression | {
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NCT02159495 | 104:113:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biological composition to cetuximab | {
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NCT01966367 | 92:123:treatment | Requirement for CD34+ stem cell selection for a second infusion of stem cells following an allogeneic stem cell transplant from a related or unrelated adult donor | {
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NCT01631617 | 1:22:chronic_disease | chronic skin diseases | {
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NCT02861950 | 1:34:chronic_disease | cyanotic congenital heart disease | {
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NCT02561104 | 14:30:treatment | Referred for cataract surgery at Parkland Memorial Hospital | {
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NCT01842399 | ,,109:112:treatment | Women over 55 years old who haven't had a period for a year will be considered menopausal and do not need a FSH test | {
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] | null |
NCT01928576 | 102:112:allergy_name,114:125:allergy_name,130:139:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to entinostat, azacitidine, or Nivolumab | {
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"azacitidine,",
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NCT02544503 | 8:49:treatment | Use of central nervous system (CNS) active drugs that block plasticity | {
"allergy_name": null,
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} | [
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0,
0,
0,
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"system",
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NCT01972113 | 21:70:chronic_disease | Subjects presenting chronic degenerative and/or inflammatory diseases | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "Status asthmatics",
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} | [
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0,
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"Subjects",
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NCT02004275 | 21:28:cancer,62:75:treatment,77:79:treatment | relapsed disease is myeloma that has previously responded to prior therapy (MR or better) and subsequently progressed | {
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NCT02159495 | 104:138:treatment | Related donor selection will be conducted in accordance with City of Hope's Department of Hematology & Hematopoietic Cell Transplantation criteria and, in the case of unrelated donor from a transplant center, will comply with the National Marrow Donor Program's (NMDP) donor selection standards | {
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... | null |
NCT02573597 | ,35:59:treatment | Narcotics within 3 hours prior to labor epidural placement | {
"allergy_name": null,
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NCT02446457 | ,64:91:chronic_disease | Have measurable disease (>= 1.5 cm in the longest diameter for nodal or extranodal disease) | {
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NCT02427581 | 39:61:cancer | Histologically confirmed diagnosis of invasive breast cancer | {
"allergy_name": null,
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"treatment": "hysterectomy"
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0,
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3
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NCT02437851 | 1:12:cancer, | Anal cancer that cannot be completely excised with a >=1 mm clear margin from surrounding tissue or where excision to obtain a clear margin would compromise sphincter function or anal canal diameter | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "chronic corneal disorder",
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... | null |
NCT01937884 | 9:29:treatment | Require artificial nutrition | {
"allergy_name": null,
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"treatment": "electrocardiographs (ECGs)"
} | [
0,
0,
0
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"Require",
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] | null |
NCT02355912 | 23:40:chronic_disease | cognitive deficits or visual impairment that would impair their ability to give informed consent or impair their ability to follow simple instructions during the experiments | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "uncontrolled seizure disorder",
"treatment": null
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NCT02939755 | 58:64:cancer | a spouse or cohabitating intimate partner of an advanced cancer patient being evaluated at the UPMC's LCC | {
"allergy_name": null,
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NCT03119363 | ,,,71:75:treatment | Who are currently over age 18 and were at least age 16 at the time of ASCT | {
"allergy_name": null,
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"treatment": "radiation treatment"
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"ASCT"
] | null |
NCT02418195 | 12:30:chronic_disease | Autoimmune glomerulonephritis | {
"allergy_name": null,
"cancer": null,
"chronic_disease": null,
"treatment": "NSAIDs"
} | [
0,
0
] | [
"Autoimmune",
"glomerulonephritis"
] | null |
NCT02373644 | 1:17:treatment | ASIS distraction | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "Psoriatic arthritis",
"treatment": null
} | [
0,
0
] | [
"ASIS",
"distraction"
] | null |
NCT03137173 | 12:44:treatment, | Use of any systemic antibacterial treatment within 14 days | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "Cardiovascular disease",
"treatment": null
} | [
0,
0,
0,
0,
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1,
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0,
0
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"Use",
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"any",
"systemic",
"antibacterial",
"treatment",
"within",
"14",
"days"
] | null |
NCT02452268 | 14:32:chronic_disease | Evaluable or measurable disease, defined as by Response Evaluation Criteria in Solid Tumors (RECIST) | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "active infection",
"treatment": null
} | [
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
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0
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"Evaluable",
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"measurable",
"disease,",
"defined",
"as",
"by",
"Response",
"Evaluation",
"Criteria",
"in",
"Solid",
"Tumors",
"(RECIST)"
] | null |
NCT02302235 | 1:20:cancer,22:45:cancer,47:50:cancer | Astrocytoma grade 4 (glioblastoma multiforme, GBM, histologically confirmed, WHO criteria) | {
"allergy_name": null,
"cancer": null,
"chronic_disease": null,
"treatment": "allo-SCT"
} | [
0,
0,
0,
0,
0,
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0,
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0
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"grade",
"4",
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"multiforme,",
"GBM,",
"histologically",
"confirmed,",
"WHO",
"criteria)"
] | null |
NCT02076906 | 15:21:cancer,90:97:treatment,147:156:treatment | The patient's cancer must have relapsed after or failed to respond to frontline curative therapy and there must not be other potentially curative treatment options available | {
"allergy_name": null,
"cancer": "fallopian tube solid tumor cancer",
"chronic_disease": null,
"treatment": "therapy"
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"other",
"potentially",
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"treatment",
"options",
"available"
] | null |
NCT02076906 | 34:50:chronic_disease | Clinically significant unrelated systemic illness | {
"allergy_name": null,
"cancer": "Tumor",
"chronic_disease": null,
"treatment": null
} | [
0,
0,
0,
0,
2
] | [
"Clinically",
"significant",
"unrelated",
"systemic",
"illness"
] | null |
NCT01686373 | ,45:51:chronic_disease | Patients must be greater than 6-months post-stroke | {
"allergy_name": null,
"cancer": "malignancy",
"chronic_disease": null,
"treatment": null
} | [
0,
0,
0,
0,
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"Patients",
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NCT02458482 | ,215:221:chronic_disease | Patients will be evaluated using the Acute Asthma Intensity Research Score (AAIRS) which has been validated at Vanderbilt University Medical Center and is currently the standard of care when triaging patients with asthma | {
"allergy_name": null,
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"treatment": "medication"
} | [
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... | null |
NCT02406885 | 20:27:treatment | Strong inducers of CYP 3A4 | {
"allergy_name": null,
"cancer": "clonal large B-cells",
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"treatment": null
} | [
0,
0,
0,
0,
0
] | [
"Strong",
"inducers",
"of",
"CYP",
"3A4"
] | null |
NCT03038620 | 39:63:treatment, | Current participation in an organized weight reduction program or within the last 1 month prior to screening for this trial | {
"allergy_name": null,
"cancer": null,
"chronic_disease": null,
"treatment": "weight reduction program"
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