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NCT02445768 | ,24:30:chronic_disease | at least 6 months post-stroke | 2 | [
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NCT02927639 | 13:33:chronic_disease | Significant cognitive disability | 2 | [
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NCT03135990 | 33:75:chronic_disease,83:115:chronic_disease,119:144:chronic_disease | A prior or present diagnosis of receptive and expressive language disorder and/or pervasive developmental disorder or severe mental retardation | 2 | [
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NCT00338377 | 20:39:cancer,41:55:cancer,59:79:cancer,83:105:chronic_disease | Patients must have metastatic melanoma, uveal melanoma or stage III in-transit or regional nodal disease. (Turnstile I) | 2 | [
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NCT02871349 | 1:17:chronic_disease | Bradyarrhythmias | 2 | [
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NCT02982564 | 16:41:treatment,, | Have completed adjuvant curative therapy at least two months to 5 years prior to recruitment | 2 | [
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NCT02050347 | 11:64:treatment,, | Available allogeneic activated peripheral blood T cell products with >=15% expression of CD19.CAR-CD28ζ determined by flow cytometry (cell dose is based on total cell numbers and not individual antileukemic cell numbers) | 2 | [
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NCT02120222 | 3:7:treatment,15:28:treatment,33:38:cancer,,,85:95:cancer | a BRAF and/or MEK inhibitor (if tumor contains the V600E or V600K mutation) for 628 metastatic disease | 2 | [
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NCT02369900 | 13:24:treatment,26:34:treatment,36:46:treatment,50:59:treatment | Infusion of epinephrine, dopamine, dobutamine or milrinone at time of enrollment | 2 | [
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NCT01983228 | ,58:78:chronic_disease | must be able to communicate effectively by telephone (no cognitive disability) | 2 | [
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NCT02319369 | 37:62:treatment | Is able and willing to provide bone marrow biopsies/aspirates as requested by the protocol | 2 | [
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NCT01787487 | 22:32:cancer,134:144:cancer,146:181:cancer,186:227:cancer | Patients with active malignancy of other type than required for this study, are not eligible with the exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma in situ of the cervix or breast | 2 | [
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NCT02519283 | 48:51:chronic_disease | Patients deemed by emergency physician to have AHF, who they plan to discharge or hold for brief ED-based observation | 2 | [
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NCT02124772 | 68:95:treatment | Must have a disease that is relapsed/refractory to all potentially curative standard treatment regimens | 2 | [
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NCT02171104 | 1:33:chronic_disease | Glycoprotein Metabolic Disorders | 2 | [
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NCT02506192 | 1:25:chronic_disease | acute Chronic Infections | 2 | [
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NCT02106988 | 43:65:treatment | with active infections requiring specific anti-infective therapy are not eligible until all signs of infections are resolved | 2 | [
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NCT02352454 | 18:38:chronic_disease | Subjects who are cognitively impaired | 2 | [
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NCT02500407 | 1:43:treatment,,69:79:treatment,88:108:treatment,112:139:treatment | Autologous stem cell transplantation (SCT) within 100 days prior to study drug, or any prior allogeneic SCT or solid organ transplantation | 2 | [
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NCT01591356 | 1:11:chronic_disease | Neuropathy (sensory and motor) =< to CTCAE grade 1 | 2 | [
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NCT02189798 | 18:44:chronic_disease,,,,,,,, | Up to a moderate sensorineural hearing loss in the low-to-mid frequencies (pure tone average ≤65 dB for 125, 250, 500, and 1000 Hz) and a severe-to-profound sensorineural hearing loss in the high frequencies (pure tone average ≥ 70 dB HL for 2,000, 3000, 4,000, and 8,000 Hz) in the contralateral (non-implanted) ear | 2 | [
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NCT01697371 | 18:31:cancer,48:58:cancer,107:126:cancer | New radiographic liver lesions consistent with metastases in patients with known pathologically confirmed non-lymphoma cancer | 2 | [
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NCT01614197 | 83:101:chronic_disease | Second or greater relapse B-cell patients are eligible at time of relapse or with refractory disease | 2 | [
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NCT02358681 | 15:20:treatment, | Receipt of an NSAID within six hours of study drug administration | 2 | [
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NCT02343042 | 14:30:chronic_disease,41:63:treatment,65:75:treatment,80:91:treatment, | Uncontrolled active infection requiring parenteral antibiotics, antivirals, or antifungals within one week prior to first dose | 2 | [
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NCT02599922 | 13:32:chronic_disease | Evidence of degenerative myopia regardless of the refractive error in the study eye | 2 | [
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NCT01313533 | 1:17:chronic_disease | Comorbid illness making 2 year survival unlikely | 2 | [
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NCT03159754 | 17:29:treatment | Patients taking theophylline | 2 | [
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NCT02496585 | 1:17:cancer | Liver metastases | 2 | [
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NCT02192398 | 31:53:chronic_disease,60:70:chronic_disease,,,105:128:chronic_disease,145:151:chronic_disease,154:181:chronic_disease,183:196:chronic_disease,198:217:chronic_disease,233:240:chronic_disease | Has known pre-existing severe cardiovascular disease (i.e. arrhythmia - prolonged QT interval > 440ms), cerebrovascular disease/accident (i.e., stroke), hepatic or renal impairment, CNS condition, metabolic condition, or history of syncope | 2 | [
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NCT03037931 | 1:28:chronic_disease,30:53:chronic_disease,55:80:chronic_disease,85:91:chronic_disease, | Acute myocardial infarction, acute coronary syndrome, transient ischemic attack, or stroke within 30 days of enrollment | 2 | [
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NCT03088072 | 21:29:allergy_name | Hypersensitivity to edoxaban | 2 | [
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NCT00483249 | 1:17:chronic_disease | Aortic aneurysms | 2 | [
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NCT02012296 | ,44:96:treatment | a minimum washout of 28 days for any other anticancer therapy prior to first dose of study drug is required (only applicable for phase I) | 2 | [
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NCT02558010 | 1:18:chronic_disease | Seizure Disorders | 2 | [
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NCT02911467 | 31:58:chronic_disease | Patients with rate-controlled atrial fibrillation/flutter | 2 | [
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NCT02535832 | 24:31:chronic_disease,33:40:chronic_disease,44:60:chronic_disease | Clinically significant hepatic, cardiac or renal impairment | 2 | [
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NCT03043807 | 1:14:treatment,21:33:treatment,35:45:treatment | Antiandrogens (e.g. bicalutamide, nilutamide) | 2 | [
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NCT02344355 | 1:8:treatment,,36:43:treatment,47:53:treatment | Therapy must begin ≤ 5 weeks after surgery or biopsy | 2 | [
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NCT02495415 | 72:90:treatment,92:105:treatment,110:128:treatment | patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study | 2 | [
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NCT03085485 | ,59:76:chronic_disease | Clinically stable in the last 4 weeks with no evidence of COPD exacerbation | 2 | [
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NCT02433626 | 9:16:cancer,18:32:cancer,34:52:cancer,54:65:cancer,70:85:cancer | Part 1: Ovarian, fallopian tube, primary peritoneal, endometrial, or cervical cancer | 2 | [
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NCT02004028 | 27:39:treatment,43:55:treatment,118:130:cancer | Participants who have had chemotherapy or radiotherapy any time prior to entering the study or at any prior time for mesothelioma. Patients receiving chemotherapy type drugs for benign conditions can participate in this trial | 2 | [
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NCT01925378 | 23:40:chronic_disease,65:68:chronic_disease,108:123:cancer | Patients with a known immunocompromised condition or a positive HIV test. Patients with a prior history of cervical cancer | 2 | [
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NCT02400463 | 34:44:cancer,154:162:treatment,166:191:treatment | Patients with a prior history of malignancy are eligible if their malignancy has been definitely treated or is in remission and does not require ongoing adjuvant or cancer-directed therapies | 2 | [
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NCT02540330 | 27:38:allergy_name,86:96:allergy_name,98:105:allergy_name,107:121:allergy_name,127:142:allergy_name | known hypersensitivity to fulvestrant or any of its formulation components including castor oil, alcohol, benzyl alcohol, and benzyl benzoate | 2 | [
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NCT02564744 | 34:68:cancer,72:104:cancer | Participants with a diagnosis of chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) | 2 | [
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NCT02646787 | 15:23:chronic_disease,25:34:chronic_disease,50:72:chronic_disease | Demonstrating delirium, psychosis or any form of Organic Brain Disorder and associated memory problems | 2 | [
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NCT01481974 | 58:70:treatment,122:149:treatment,173:194:treatment | Be receiving any investigational drug (a drug other than Treprostinil administered under an IND) or participating in any other investigational study, with the exception of alemtuzumab (Campath) | 2 | [
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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 | 2 | [
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NCT02360579 | 1:18:treatment,26:46:treatment,52:64:treatment | Antibiotics (ABX) of the aminoglycoside group (ie, streptomycin, gentamicin); except those who are skin-test negative for gentamicin hypersensitivity | 2 | [
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NCT01434472 | 71:86:cancer,88:125:cancer,127:148:cancer,,213:244:treatment | Patients must have a histologically confirmed diagnosis of aggressive B-cell lymphoma (diffuse large B-cell lymphoma [DLBCL], Burkitt lymphoma [BL], etc.) expressing the CD20 antigen and have failed at least one prior standard systemic therapy | 2 | [
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NCT03162731 | 1:27:cancer,31:54:cancer,86:102:treatment | superficial bladder cancer or in situ cervical cancer that has undergone potentially curative therapy | 2 | [
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NCT02058095 | 13:28:treatment,33:53:chronic_disease,86:96:treatment | Patients on PDEV inhibition for erectile dysfunction who are not willing to stop the medication for the duration of the study | 2 | [
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NCT02474667 | 1:11:treatment, | Study drug can be administered starting within 30 hours after restoration of blood flow to the engrafted kidney | 2 | [
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NCT01940757 | 32:45:chronic_disease | Positive confirmatory test for HIV infection | 2 | [
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NCT02864862 | 8:29:chronic_disease,31:43:chronic_disease,57:76:treatment | severe parafunctional habits, malocclusion or intent of orthodontic therapy in the future | 2 | [
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NCT01676259 | 18:28:allergy_name | Known allergy to sesame oil | 2 | [
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NCT02514083 | ,58:67:chronic_disease | Night sweats for more than one month without evidence of infection | 2 | [
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NCT02122081 | 24:33:treatment,43:46:cancer,48:51:cancer,55:58:cancer,68:83:treatment | For patients receiving treatment of their AML, MDS or ALL prior to transplantation | 2 | [
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NCT02709655 | 17:48:chronic_disease | The patient has Major depressive disorder (MDD), diagnosed according to DSM-5™ | 2 | [
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NCT00887146 | 21:42:treatment,73:82:treatment,99:107:chronic_disease | Receiving any other investigational agent that would be considered as a treatment for the primary neoplasm | 2 | [
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NCT01684904 | 71:89:treatment | Surgical consultation to confirm that patient will be able to undergo curative resection after completion of PCT prior to registration | 2 | [
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NCT02389309 | 34:57:chronic_disease,,97:122:chronic_disease,135:158:chronic_disease,165:188:treatment | Patients with evidence of recent intratumoral hemorrhage (within 3 months of study enrollment), gastrointestinal bleeding, history of coronary artery disease or on anticoagulation therapy | 2 | [
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NCT01604512 | 1:15:chronic_disease | Claustrophobia | 2 | [
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NCT02219711 | 14:20:cancer | Other active cancer | 2 | [
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NCT02509546 | 21:24:treatment, | Expected to undergo HCT within 120 days of enrollment | 2 | [
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NCT02914483 | 1:19:chronic_disease | anginal equivalent symptoms at rest | 2 | [
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NCT02172651 | 25:44:treatment,56:75:treatment,77:92:treatment,94:111:treatment,113:126:treatment,131:153:treatment | Concurrent use of other anti-cancer therapy, including chemotherapy agents, targeted agents, biological agents, immunotherapy, or investigational agents not otherwise specified in this protocol | 2 | [
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