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NCT02451215 | 18:28:cancer | Other high grade CNS tumors | 1 | [
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NCT02369406 | 1:16:treatment | Hospitalization for severe medical illness | 1 | [
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NCT03097536 | 1:17:chronic_disease | Chronic migraine | 1 | [
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NCT02589938 | 11:23:treatment | Receiving chemotherapy during study period | 1 | [
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NCT00716066 | 45:79:chronic_disease | Patients who are serologically positive for human immunodeficiency virus (HIV) | 1 | [
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NCT02392572 | 4:13:treatment,29:37:treatment,42:46:chronic_disease,,64:76:treatment | No treatment with high dose steroids for GVHD (up to >/= 20 mg Prednisolone or equivalent per day) | 1 | [
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NCT01525901 | 21:30:cancer | active or suspected neoplasia | 1 | [
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NCT01737502 | 37:56:treatment | Recovered from the toxic effects of radiation treatment before study entry | 1 | [
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NCT02573376 | 76:86:treatment,97:110:treatment,112:157:treatment,159:171:treatment,173:183:treatment | Medications not recommended per the SOF/LDV prescribing information (e.g., tipranavir and other P-gp inducers, tenofovir disoproxil fumarate plus cobicistat, rosuvastatin, amiodarone) | 1 | [
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NCT01975597 | 36:48:chronic_disease | Patients with active, uncontrolled coagulopathy | 1 | [
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NCT01822522 | ,,62:74:chronic_disease, | Lipase < 2.0 x ULN and no radiologic or clinical evidence of pancreatitis (within 1 week of study entry) | 1 | [
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NCT02233868 | 17:20:chronic_disease | Have a positive HIV test (clinical laboratory results, medical history) | 1 | [
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NCT02015390 | 14:27:chronic_disease | Disseminated osteomyelitis throughout the bone | 1 | [
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NCT01614197 | 1:33:treatment,72:103:treatment,108:117:treatment,119:132:treatment,137:150:treatment | Enzyme inducing Anti-convulsants: Patients who are currently receiving enzyme inducing anticonvulsants (ie phenytoin, phenobarbitol, or carbamazepine) are not eligible | 1 | [
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NCT02516696 | 13:25:chronic_disease,29:49:chronic_disease,136:145:treatment | Subject has active viral or bacterial infections or any coexisting medical problem that would significantly increase the risks of this treatment program | 1 | [
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NCT02834403 | 23:32:treatment, | Patients who received docetaxel at any line of treatment within the past 12 months | 1 | [
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NCT01614990 | 1:14:chronic_disease,, | renal failure (creatinine >1.5 mg/dL) | 1 | [
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NCT02382419 | 12:56:chronic_disease,58:71:chronic_disease,73:82:chronic_disease,87:114:chronic_disease,143:152:treatment | Documented human immunodeficiency virus (HIV) infection, genital warts, chancroid, or pelvic inflammatory disease that will require long term treatment | 1 | [
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NCT02530463 | ,,,155:188:treatment | Males who have partners of childbearing potential must agree to use an effective contraceptive method during the study and a period of 31 weeks after the last dose of investigational drug | 1 | [
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NCT02506192 | 1:11:chronic_disease | Vasculitis | 1 | [
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NCT01703117 | 27:36:treatment, | Subjects who have been on donepezil for longer than 5 years | 1 | [
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NCT02706249 | 13:37:chronic_disease,44:59:chronic_disease,61:88:chronic_disease,90:115:chronic_disease,117:140:chronic_disease | Established hereditary thrombophilia (e.g. Factor V Leiden, G20210 prothrombin mutation, protein C or S deficiency, antithrombin deficiency) | 1 | [
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NCT02519322 | 1:23:chronic_disease | Cardiovascular disease-related requirement for daily supplemental oxygen | 1 | [
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NCT01703117 | 13:39:chronic_disease,48:64:chronic_disease,66:79:chronic_disease,81:104:chronic_disease,106:123:chronic_disease,115:123:chronic_disease,125:151:chronic_disease,153:165:chronic_disease | Significant neuropsychiatric illnesses such as bipolar disorder, schizophrenia, moderate-severe anxiety, vascular dementia, Creutzfeldt-Jakob dementia, HIV dementia, and dementia in other specified diseases | 1 | [
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NCT03058146 | 12:20:chronic_disease | History of diabetes | 1 | [
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NCT02346526 | 1:20:cancer,36:45:treatment,49:80:treatment | Visceral metastases as assessed by abdominal or pelvic computed tomography (CT) or other imaging modality | 1 | [
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NCT02576444 | 41:66:chronic_disease,73:99:chronic_disease,116:131:treatment | Refractory nausea and vomiting, chronic gastrointestinal diseases (e.g. inflammatory bowel disease) or significant bowel resection that would preclude adequate absorption | 1 | [
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NCT02262806 | 25:37:chronic_disease | Decrease in episodes of pancreatitis | 1 | [
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NCT02710396 | 1:36:cancer | squamous cell carcinoma of the skin | 1 | [
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NCT02513485 | 27:40:chronic_disease,42:66:chronic_disease,79:92:chronic_disease,94:103:chronic_disease,105:115:chronic_disease,150:168:chronic_disease,170:178:chronic_disease | History of the following: schizophrenia, schizoaffective disorder, other (non mood disorder) psychosis, depression secondary to a medical condition, mental retardation, dementia, or delirium | 1 | [
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NCT02577406 | 65:78:treatment | Subject is eligible for and willing to receive the pre-selected CCR treatment option, according to the investigator's assessment | 1 | [
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NCT02419560 | 16:32:chronic_disease | Subject has an active infection | 1 | [
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NCT02259504 | 79:88:treatment | Subject with social, medical, or psychological conditions that interfere with treatment and follow-up evaluation | 1 | [
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NCT02513797 | 20:51:treatment, | Based on screening computed tomography angiography performed within 90 days prior to study intervention as confirmed by the core lab | 1 | [
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NCT03053453 | 70:87:chronic_disease | Patients will be screened for eligibility based on whether they have chronic knee pain as a result of an arthritis-related condition | 1 | [
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NCT01059786 | 13:16:treatment,,,, | Evidence of HCL by flow cytometry of blood or a solid (lymph node) mass, confirmed by the Laboratory of Pathology, NCI, including positivity for CD19, CD22, CD20, and CD11c | 1 | [
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NCT01532687 | ,45:68:treatment | for at least 21 days after the last dose of investigational product | 1 | [
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NCT02270970 | 1:7:cancer,,54:80:cancer,92:116:cancer | Cancer within 5 years (except for completely excised cervical carcinoma in situ or excised non-melanoma skin cancer) | 1 | [
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NCT02162420 | 14:55:chronic_disease | Diagnosis of DC with a triad of mucocutaneous features | 1 | [
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NCT03054519 | 1:23:chronic_disease | Critical limb ischemia | 1 | [
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NCT02461927 | 9:17:chronic_disease | Current dementia | 1 | [
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NCT01128816 | 1:19:chronic_disease | Active myocarditis | 1 | [
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NCT02514915 | 23:50:cancer | Patients must have an extra-cranial primary tumor diagnosis | 1 | [
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NCT02446457 | ,,,78:87:treatment | Absolute neutrophil count (ANC) >= 1.0 x 10^9/L, performed within 28 days of treatment initiation | 1 | [
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NCT01872975 | 12:35:cancer,48:63:cancer,80:94:treatment,99:109:cancer,114:150:cancer, | History of non-breast malignancies (except for in situ cancers treated only by local excision and basal cell and squamous cell carcinomas of the skin) within 5 years prior to randomization | 1 | [
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NCT02044120 | 30:47:cancer,,97:132:cancer,136:160:cancer | Other clinically significant malignant disease diagnosed within the previous 5 years, excluding intra-epithelial cervical neoplasia or non-melanoma skin cancer | 1 | [
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NCT02098161 | ,58:88:treatment,,111:121:treatment,130:144:treatment,179:214:treatment,261:271:treatment | Patients who are currently receiving chronic (> 14 days) treatment with corticosteroids at a dose >= 10 mg of prednisone (or its glucocorticoid equivalent) per day, or any other chronic immunosuppressive treatment that cannot be discontinued prior to starting study drug | 1 | [
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NCT01618357 | ,,,41:57:cancer | Bilirubin ≤ 1.5 mg/dL (≤ 3.0 mg/dL with liver metastasis) | 1 | [
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NCT03144245 | ,22:31:treatment,32:48:treatment,58:72:chronic_disease,,99:119:treatment | No more than 3 prior induction/salvage regimens to treat active disease, and no more than 1 prior stem cell transplant | 1 | [
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NCT02058095 | ,,,,206:223:chronic_disease, | a minimal distance on 6-minute walk of equal or >450 meters will be recruited and calculated creatinine clearance of equal or less than 90 ml/min and greater than 30 ml/min, using the (MDRD-measurement of renal dysfunction, formula) assessed within the past 36 months | 1 | [
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NCT02876510 | 106:113:treatment | Patient is a candidate for a maximum of one further line of established therapy (prior to treatment with ACTolog) | 1 | [
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NCT03168659 | ,25:45:treatment | failure of at least one anti-arrhythmic drug | 1 | [
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NCT01627821 | 88:126:treatment,,,194:224:treatment,255:267:treatment | Patients on Optimal Medical Management (OMM) as defined in Section 9.2 OR dependent on intra-aortic balloon counter-pulsation for 7 days OR other temporary (indicated for 30 days use, or less) mechanical circulatory support for 7 days, OR supported with IV inotropes for 7 days and failing to respond | 1 | [
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NCT02496585 | 9:18:treatment,24:36:treatment,48:57:treatment,61:81:treatment,91:101:cancer | Ongoing treatment with radiotherapy to thorax, cytotoxic or biological therapies for this malignancy | 1 | [
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NCT03152058 | 58:70:allergy_name | Known contraindications or relative contraindications to certolizumab | 1 | [
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NCT02353728 | 1:23:chronic_disease | uncontrolled infection | 1 | [
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NCT02721303 | 63:79:treatment | Use of any medication known to significantly affect appetite (anti-depressants are allowable) | 1 | [
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NCT02513797 | 1:16:treatment | medical illness or comorbidity which would make the subject unsuitable to participate in this study as determined by the clinical site Primary Investigator | 1 | [
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NCT02665338 | 1:9:treatment | caffeine | 1 | [
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NCT01626079 | 18:56:treatment | Subjects in whom transesophageal echocardiography (TEE) is contraindicated or high risk | 1 | [
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NCT02863809 | 41:58:chronic_disease | Inability to wear a contact lens due to lid abnormalities or shortened fornix | 1 | [
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NCT02957149 | 39:63:cancer | Newly diagnosed, clinically localized prostatic adenocarcinoma | 1 | [
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NCT02535923 | 82:105:chronic_disease,,,121:140:chronic_disease,,,,,172:188:chronic_disease | Diagnostic and Statistical Manual of Disorders, 5th edition (DSM 5) diagnosis of schizophrenic disorders (295.0-295.9), affective psychoses (296.0-296.1, 296.4-296.8), or major depression with psychotic features (296.24, 296.34) | 1 | [
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