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NCT02073097 | ,118:129:treatment | breastfeeding women are excluded from this study; breastfeeding should be discontinued if the mother is treated with carfilzomib | 2 | [
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NCT02122185 | 20:44:treatment,37:44:treatment,54:80:treatment | subjects receiving neoadjuvant chemotherapy for whom interval debulking surgery (assuming adequate response to therapy) is not planned | 2 | [
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NCT01835626 | ,,,100:110:treatment | Verify the pregnancy status of females of reproductive potential within 7 days prior to initiating vismodegib | 2 | [
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NCT02826681 | 13:29:treatment, | Subjects on sleep medication must be on a stable dose for at least 6 months prior screening | 2 | [
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NCT01954173 | 30:40:treatment | Patients treated with simple cystectomy with macroscopically negative margins are eligible for this study | 2 | [
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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 | 2 | [
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NCT02312596 | 10:48:treatment, | Received another investigational device or drug within 30 days of enrollment | 2 | [
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NCT02378428 | 18:65:treatment,58:65:treatment,,,106:123:treatment,106:115:treatment | Patients for who CEM (carboplatin, etoposide, melphalan) therapy is administered within 30 days prior to 131I-MIBG therapy or for whom this therapy is planned within 30 days following administration of 131I-MIBG | 2 | [
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NCT02479698 | 5:22:chronic_disease,12:21:chronic_disease,70:89:treatment,137:149:treatment | For fungal infections patients must be receiving definitive systemic anti-fungal therapy and have no signs of progressing infection for 1 week prior to enrollment | 2 | [
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NCT02314377 | 24:35:treatment,45:69:treatment,81:118:treatment,,143:154:treatment | Patients must not have core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to bevacizumab | 2 | [
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NCT01756040 | 8:16:chronic_disease | Severe asphyxia | 2 | [
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NCT02913430 | 40:51:treatment,59:67:treatment,69:81:treatment,85:103:treatment | Patients must have previously received palbociclib in the adjuvant, neo-adjuvant or metastatic setting | 2 | [
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NCT01865162 | 16:44:treatment | ≥ weeks from a non-nitrosourea chemotherapy (all [a-c] in order to allow recovery from the potential of severe toxicity related to these treatments) | 2 | [
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NCT01415882 | 34:59:chronic_disease,71:90:chronic_disease,92:116:chronic_disease,118:124:chronic_disease,129:150:chronic_disease, | Evidence of current uncontrolled cardiovascular conditions, including cardiac arrhythmias, congestive heart failure, angina, or myocardial infarction within the past 6 months | 2 | [
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NCT02565901 | 1:16:treatment,20:29:treatment,91:100:treatment | bisphosphonates or denosumab should not be initiated after registration and during active treatment | 2 | [
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NCT02468453 | 34:43:treatment,55:61:cancer,86:97:cancer,156:173:chronic_disease,187:231:cancer | Having or undergoing any form of treatment for active cancer, or having a history of skin cancer or any other cancer in the areas to be treated, including actinic keratosis, presence of malignant or pre-malignant pigmented lesions | 2 | [
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NCT02554812 | 49:61:cancer,63:68:cancer,70:75:cancer,77:85:cancer,111:127:treatment | Combination B: Phase 1b, patients with advanced solid tumors (NSCLC, SCCHN, melanoma) that have progressed on standard therapy or for which no standard therapy is available, and Phase 2, patients with NSCLC, melanoma, or SCCHN | 2 | [
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NCT02356861 | 5:40:chronic_disease | Had Gulf War Veterans' Illnesses (GWVI), but did not answer 'Yes' to the following questions: 1) Difficulty concentrating and/or 2) Difficulty remembering recent information | 2 | [
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NCT02723994 | 1:27:chronic_disease | Trisomy 21 (Down syndrome) | 2 | [
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NCT02365766 | 1:17:chronic_disease, | Hearing impaired ≥grade 2 as assessed by treating physician (may or may not be enrolled in a monitoring program) | 2 | [
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NCT01726257 | 1:12:chronic_disease | Psychiatric or other condition that may interfere with the study | 2 | [
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NCT02259621 | 1:28:treatment,33:58:treatment,,73:83:treatment,135:153:chronic_disease | Inhaled or topical steroids and adrenal replacement doses > 10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease | 2 | [
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NCT02404870 | 17:32:chronic_disease,36:57:chronic_disease,100:109:chronic_disease,126:135:treatment | Past history of eating disorder or psychiatric disorders, including severe depression, anxiety, or psychosis or presently on treatment with medications for any of these conditions | 2 | [
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NCT01970176 | 15:35:chronic_disease,71:87:chronic_disease,99:124:chronic_disease | Patients with retinitis pigmentosa, previous diagnosis of nonischemic optic neuropathy, untreated proliferative retinopathy or unexplained visual disturbance | 2 | [
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NCT01954576 | 11:21:cancer,43:55:treatment,,189:199:cancer,203:238:cancer,288:319:cancer | Any other malignancy that required active chemotherapy within the previous 12 months prior to registration and the disease is not currently progressing and/or metastatic. The exception is basal cell or squamous cell carcinoma of the skin, which were treated with local resection only or carcinoma in situ of the cervix | 2 | [
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NCT02592707 | 27:32:allergy_name,37:41:allergy_name,46:50:allergy_name,68:94:allergy_name | Known hypersensitivity to 177Lu, to DOTA, to JR11 or to any of the excipients of 177Lu-OPS201 | 2 | [
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NCT03035773 | 11:17:cancer | Had their cancer care primarily managed by either JHMI or PRMC, with JHMI or PRMC primarily responsible for the patients' survivorship care | 2 | [
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NCT02542202 | 1:51:chronic_disease,61:80:chronic_disease,121:134:treatment, | Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days prior to registration | 2 | [
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NCT02876302 | ,,53:63:treatment,65:76:treatment,82:98:treatment | Pregnant women are excluded from this study because paclitaxel, doxorubicin, and cyclophosphamide have the potential for teratogenic or abortifacient effects | 2 | [
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NCT02900794 | 21:37:chronic_disease,39:58:chronic_disease,60:81:chronic_disease | Patients with known immunodeficiency, ciliary dysfunction, uncontrolled diabetes | 2 | [
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NCT02369458 | 31:53:treatment | Currently receiving any other investigational agents | 2 | [
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NCT02451215 | 1:11:cancer | Meningioma | 2 | [
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NCT02035137 | 18:49:treatment | They have had an allogeneic stem cell transplant (received stem cell from someone else) | 2 | [
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NCT01986205 | 7:27:chronic_disease,31:58:chronic_disease,68:86:chronic_disease | Major psychiatric disorder or degenerative mental disease (such as multiple sclerosis) | 2 | [
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NCT01823198 | ,,,,136:158:treatment | Pregnancy: positive pregnancy test in a woman with child bearing potential defined as not post-menopausal for 12 months or no previous surgical sterilization | 2 | [
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NCT02996227 | 1:15:treatment,56:64:treatment,68:78:treatment | Anticoagulants considered to be a contraindication for epidural or TAP blocks | 2 | [
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NCT02074436 | 1:35:treatment, | Hematopoietic stem cell transplant recipient within 100 days post-transplant | 2 | [
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NCT01904136 | 1:41:chronic_disease, | Central nervous system (CNS) involvement within 3 months | 2 | [
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NCT02460900 | 51:62:allergy_name | Previous allergic reaction or hypersensitivity to Varenicline (by participant report ever in lifetime) | 2 | [
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NCT02268448 | 18:66:chronic_disease | Known history of central or peripheral nervous system dysfunction | 2 | [
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NCT02172651 | 16:34:treatment,42:61:treatment,82:95:chronic_disease,171:194:chronic_disease | Regular use of thiazide diuretics (i.e., hydrochlorothiazide), which can lead to hypercalcemia, and unwillingness or inability to discontinue or switch to an alternative anti-hypertensive agent | 2 | [
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NCT02819843 | 67:83:chronic_disease | Previously infected, with evidence of immunity and no evidence of active hepatitis | 2 | [
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NCT02120222 | 26:49:chronic_disease, | known to be positive for hepatitis C virus (HCV) ribonucleic acid (RNA) | 2 | [
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NCT02541903 | 43:47:chronic_disease | Histologically or cytologically confirmed PSCC | 2 | [
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NCT02470897 | 1:12:chronic_disease | Scleroderma | 2 | [
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NCT02910700 | 15:40:cancer | Patients with melanoma brain metastases are allowed | 2 | [
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NCT02471833 | 12:18:chronic_disease | History of stroke | 2 | [
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NCT02519322 | 1:20:chronic_disease, | Uncontrolled angina within the 3 months prior to consent | 2 | [
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NCT02674529 | 43:70:treatment | Have a medical condition that contradicts treatment with escitalopram | 2 | [
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NCT02429830 | 1:5:chronic_disease,30:41:treatment, | GERD symptoms, in absence of PPI therapy (minimum 7 days) | 2 | [
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NCT02759211 | 26:42:treatment | Current participation in physical therapy | 2 | [
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NCT02555189 | 23:46:treatment,35:46:treatment,48:61:treatment,63:91:treatment,93:107:treatment,109:133:treatment,135:147:treatment | Use of any prohibited concomitant medications: immunotherapy, 5 alpha reductase inhibitors, spironolactone, diethylstilbestrol (DES), ketoconazole, newer medications targeting ARs | 2 | [
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NCT03068442 | 24:38:chronic_disease,50:69:chronic_disease,110:130:chronic_disease,134:151:cancer,153:165:chronic_disease,, | Other known sources of cardioembolism, including atrial fibrillation, mechanical heart valve, left atrial or ventricular thrombus or intracardiac mass, endocarditis, EF <30% | 2 | [
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NCT02178566 | 35:47:allergy_name | Known hypersensitivity to inhaled nitric oxide | 2 | [
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NCT02865135 | 7:13:cancer, | Other cancer in the past 5 years | 2 | [
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NCT02695043 | 29:55:chronic_disease | Trauma related intracranial neuroimaging abnormalities | 2 | [
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NCT02483910 | 21:105:treatment, | Currently receiving Direct Instruction Language for Learning (DI-LL) or participation in a DI-LL program in the past 2 years | 2 | [
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NCT01505569 | 1:8:chronic_disease,,,,,, | Hepatic: AST or ALT ≤ 2.5 x upper limits of normal (ULN), if hepatic involvement < 5 x ULN; bilirubin ≤ 2.0 x upper limits of normal (ULN) | 2 | [
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