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NCT01976585 | ,72:94:treatment | Patients must have at least one site of disease that is accessible for intratumoral injection percutaneously (e.g. inguinal, axillary, cervical, or subcutaneous) | 3 | [
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NCT02464878 | 34:37:chronic_disease,,, | Clinical history compatible with T1D with disease onset < 40 years of age | 3 | [
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NCT02048722 | 18:62:chronic_disease,92:118:chronic_disease,144:161:treatment | Known history of human immunodeficiency virus (HIV) infection or current chronic or active hepatitis B or C infection requiring treatment with antiviral therapy | 3 | [
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NCT02579967 | 110:126:allergy_name,128:136:allergy_name,138:149:allergy_name,151:160:allergy_name,162:165:allergy_name,167:172:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to agents (cyclophosphamide, busulfan, pentostatin, sirolimus, MMF, G-CSF) used in the study | 3 | [
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NCT02378428 | 18:34:chronic_disease,57:67:treatment,69:80:treatment,84:95:treatment | Patients with an active infection requiring intravenous antivirals, antibiotics or antifungals | 3 | [
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NCT01306045 | 1:22:chronic_disease | Uncontrolled diabetes | 3 | [
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NCT02371720 | 30:41:treatment | Patient or caregiver refuses Hydroxyurea | 3 | [
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NCT01174108 | 1:42:chronic_disease,76:86:chronic_disease,95:104:chronic_disease | Paroxysmal nocturnal hemoglobinuria (PNH) associated with life-threatening thrombosis, and/or cytopenia, and/or transfusion dependence and/or recurrent and debilitating hemolytic crisis | 3 | [
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NCT02209545 | 32:43:treatment,45:57:treatment,62:86:treatment | Can be previously treated with Depo-Lupron, Depo-Provera, or Oral Contraceptive pills | 3 | [
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NCT03003780 | 1:10:chronic_disease | Hypoxemia during 6MWT | 3 | [
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NCT01835626 | 27:48:chronic_disease,196:216:treatment,322:331:treatment | History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates use of an investigational drug or that might affect interpretation of the results of the study or renders the patient at high risk form... | 3 | [
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NCT02905591 | 1:10:treatment | quinidine | 3 | [
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NCT02419495 | 1:14:treatment, | Major surgery within four weeks before consent date | 3 | [
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NCT02089607 | 1:30:treatment | Proximal aortic fixation zone | 3 | [
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NCT01961557 | 1:13:chronic_disease | spina bifida | 3 | [
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NCT02859142 | 1:10:chronic_disease | cirrhosis | 3 | [
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NCT00713492 | 41:53:treatment | Positive result on urine drug screen or breathalyzer test during initial or update visit under the screening protocol (14-AA-0181) most proximal to enrollment | 3 | [
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NCT01429337 | ,,78:89:treatment, | Sexually active males unless they use condom during intercourse while taking midostaurin and for at least 3 months after the last exposure to drug | 3 | [
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NCT02841540 | 36:44:cancer | Diagnosis of a core binding factor leukemia (t(8;21), t(16;16) or inv(16)) | 3 | [
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NCT01880567 | 21:24:cancer | Relapsed/refractory MCL: Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form | 3 | [
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NCT03118232 | 16:37:treatment | Minimal use of chlorhexidine bathing | 3 | [
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NCT02523443 | 1:10:chronic_disease | Cirrhotic patients | 3 | [
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NCT02776475 | 15:37:chronic_disease | Patients with cognitive disabilities or those lacking the mental capacity to understand and answer questionnaires | 3 | [
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NCT02088554 | 18:35:treatment | Patient requires emergency surgery | 3 | [
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NCT03069469 | 29:41:cancer,57:62:cancer,73:91:treatment | Patients must have advanced solid tumors or symptomatic DTGCT for which surgical resection is not an option | 3 | [
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NCT02503358 | 1:15:treatment, | Major surgical procedure within 21 days prior to enrollment | 3 | [
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NCT01666665 | 1:14:chronic_disease | liver disease | 3 | [
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NCT02139436 | 12:29:chronic_disease | history of bleeding disorder | 3 | [
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NCT02762032 | 1:17:treatment | Muscle relaxants | 3 | [
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NCT03074240 | 1:26:chronic_disease | Severe hepatic impairment | 3 | [
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NCT01970345 | 23:28:allergy_name | History of allergy to IGF-1 | 3 | [
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NCT02553941 | 18:30:cancer | History of other malignancies | 3 | [
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NCT01697371 | 1:19:treatment | Prior radiotherapy to the liver | 3 | [
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NCT02762006 | 12:39:treatment | History of allogeneic organ transplant | 3 | [
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NCT01648023 | 26:57:allergy_name | Any contraindication for hepatic embolization procedures | 3 | [
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NCT02301663 | 12:26:chronic_disease,28:37:chronic_disease,42:62:chronic_disease | History of cardiovascular, pulmonary, or neurological disease | 3 | [
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NCT02197351 | 17:39:treatment,50:61:treatment,63:74:treatment,76:84:treatment,86:93:treatment,95:105:treatment,111:120:treatment,124:137:treatment | Patients taking anti-thrombotic agents including clopidogrel, ticlopidine, coumadin, heparin, enoxaparin, and direct II or Xa inhibitors | 3 | [
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NCT02473536 | 1:13:treatment,26:38:cancer,48:62:cancer | Radiographic evidence of renal cancer with IVC tumor thrombus | 3 | [
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NCT03115424 | 74:91:treatment | Seen at Mayo Clinic Nutrition Clinic and have received authorization for bariatric surgery | 3 | [
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NCT02816736 | 56:67:chronic_disease | Any one or more of the following objective findings of advanced HF | 3 | [
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NCT02636283 | 1:12:cancer | skin cancer | 3 | [
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NCT02078102 | 1:30:cancer | Diffuse large B cell lymphoma | 3 | [
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NCT02685358 | 22:38:chronic_disease | Patients with recent suicide attempts | 3 | [
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NCT01730794 | 15:31:treatment,33:40:treatment,45:57:treatment | Patients with major esophageal, gastric and oral surgery | 3 | [
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NCT02143830 | 1:21:treatment | platelet transfusion dependenc | 3 | [
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NCT02127398 | 14:40:chronic_disease | Diagnosis of inflammatory bowel disease | 3 | [
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NCT02037048 | 1:17:cancer, | tumors of the GC are defined as originating within 5 cm of the GEJ | 3 | [
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NCT02959489 | 41:66:treatment | Individuals willing to participate in a randomized clinical trial of amyloid imaging disclosure | 3 | [
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NCT02159027 | 27:30:allergy_name | Known hypersensitivity to MVC or its excipients | 3 | [
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NCT03078504 | 13:24:treatment,25:40:treatment,52:66:treatment,55:66:treatment,71:81:treatment,83:91:treatment,93:104:treatment | intravenous vasopressor/inotropic agent other than norepinephrine (ie dobutamine, dopamine, vasopressin, epinephrine) | 3 | [
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NCT03069716 | 19:25:chronic_disease | activity-limiting angina | 3 | [
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NCT02080221 | 159:167:treatment | Patients with serious medical risk factors involving any of the major organ systems such that the investigator considers it unsafe for the patient to receive FOLFOX-A | 3 | [
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NCT03137173 | 9:15:chronic_disease,64:87:chronic_disease,89:97:chronic_disease,102:118:chronic_disease,120:141:chronic_disease,175:184:chronic_disease,198:212:chronic_disease,295:311:chronic_disease | Primary ABSSSI due to or associated with any of the following: diabetic foot infection, gangrene, or perianal abscess; concomitant infection at another site; infected burns; decubitus, chronic, or ischemic ulcer; evolving necrotizing process; infections at vascular catheter sites or involving thrombophlebitis | 3 | [
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NCT00147056 | 25:36:chronic_disease | Untreated, uncontrolled Sleep apnea | 3 | [
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NCT03100435 | 107:128:chronic_disease,130:151:chronic_disease,153:160:cancer,162:179:chronic_disease,181:210:chronic_disease,215:243:chronic_disease | Subjects with uncontrolled or debilitating medical conditions, including but not limited to subjects with uncontrolled diabetes, hematologic disorders, cancers, immunosuppression, severe cardiovascular disease, or uncontrolled thyroid disease | 3 | [
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NCT02474368 | 1:12:treatment | Bevacizumab | 3 | [
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NCT02947165 | 26:58:cancer,,161:177:treatment,199:212:treatment,302:307:cancer,321:336:treatment,347:351:cancer,362:365:cancer,376:383:cancer,414:419:cancer | Expansion: Patients with advanced/metastatic solid tumors, with at least one measurable lesion as determined by RECIST version 1.1, who have progressed despite standard therapy following their last prior therapy or are intolerant to standard therapy and fit into one of the following groups: Group 1: NSCLC resistant to ... | 3 | [
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NCT01915095 | 5:25:chronic_disease | Any debilitating disease prior to the SCI that caused exercise intolerance | 3 | [
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NCT00914823 | ,,20:49:chronic_disease | Men and women with hypogonadotropic hypogonadism | 3 | [
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NCT02822001 | 15:38:chronic_disease,, | Patients with Impaired Renal Function with a have a known estimated CrCl<30 ml/min | 3 | [
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NCT02464878 | 13:23:chronic_disease | symptomatic gallstones | 3 | [
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NCT02979366 | 24:37:chronic_disease | history of significant liver disease | 3 | [
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NCT00230607 | 1:11:treatment | genotyping | 3 | [
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NCT03115424 | 16:35:chronic_disease | Active, severe psychiatric disease | 3 | [
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NCT02953509 | 16:51:cancer | Phase 1b only: B-cell non-Hodgkin's lymphoma (NHL), relapsed or refractory to standard approved therapies | 3 | [
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NCT02561104 | 91:102:treatment | Poor dilating pupil such that the iris is not peripheral to the intended diameter for the capsulotomy | 3 | [
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NCT01434472 | ,30:48:treatment,56:74:treatment,76:91:treatment,93:116:treatment | < 5 half-lives for all other anti-cancer agents (e.g., targeted therapies, corticosteroids, immunomodulatory agents, etc.) | 3 | [
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NCT02767518 | 1:24:chronic_disease | Acute aortic dissection | 3 | [
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NCT01946074 | ,73:95:chronic_disease,83:95:chronic_disease,135:154:chronic_disease,168:181:chronic_disease,183:197:chronic_disease,199:220:chronic_disease,222:253:chronic_disease,255:273:chronic_disease,284:294:treatment,296:335:treatment,337:345:chronic_disease,349:364:treatment,366:377:treatment,405:430:chronic_disease,, | Subject has history (within previous 5 years) of clinically significant pulmonary hypertension, uncontrolled systemic hypertension or hypertensive crisis, symptomatic heart failure, cardiomyopathy, myocardial infarction, unstable/severe angina pectoris, cardiac arrhythmia requiring medication, coronary/peripheral arter... | 3 | [
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NCT01639508 | 43:72:cancer | The subject has a pathologic diagnosis of non-small cell lung carcinoma that is metastatic or unresectable | 3 | [
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NCT01978509 | 1:8:chronic_disease | Ascites | 3 | [
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NCT02522715 | 1:13:treatment, | Ketoconazole; approximate half-life: 8 hours; washout period required: 48 hours | 3 | [
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NCT01684904 | 13:38:chronic_disease | Evidence of tracheoesophageal fistula or invasion into the trachea or major bronchi | 3 | [
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NCT02553265 | 17:51:treatment | Patients taking monoamine oxidase (MAO)-inhibitors | 3 | [
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NCT02451423 | 1:40:treatment,50:88:treatment,119:129:treatment,131:144:treatment,146:162:treatment,164:176:treatment,178:190:treatment,192:203:treatment,209:253:treatment | Treatment with systemic corticosteroids or other systemic immunosuppressive medications (including but not limited to prednisone, dexamethasone, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor [anti-TNF] agents | 3 | [
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NCT01562626 | 17:25:treatment | Currently using warfarin | 3 | [
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NCT02393794 | 1:31:chronic_disease,,, | Congestive heart failure (CHF) that meets New York Heart Association (NYHA) Class II to IV definitions and/or ejection fraction | 3 | [
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NCT02706288 | 45:53:chronic_disease,84:93:chronic_disease,95:101:chronic_disease,105:127:chronic_disease | Significant organ system dysfunction (e.g., diabetes requiring medications, severe pulmonary, kidney or cardiovascular disease) | 3 | [
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NCT02378714 | 1:37:chronic_disease | cirrhosis or end-stage liver disease | 3 | [
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NCT01697865 | 1:25:chronic_disease,33:65:chronic_disease,82:104:chronic_disease | Shoulder pseudoparalysis due to chronic rotator cuff dysfunction with or without glenohumeral arthritis | 3 | [
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NCT03149783 | 1:16:treatment | plastic surgery | 3 | [
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NCT02646787 | 1:25:chronic_disease | Developmental disability | 3 | [
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NCT01434316 | 39:48:treatment | Patients who have previously received SCH727965 | 3 | [
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NCT01812174 | 1:13:chronic_disease | mentally ill | 3 | [
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