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NCT03104699 | 15:58:cancer,78:87:treatment,93:154:treatment | subjects with castration-resistant prostate cancer (CRPC), who may remain on treatment with luteinizing hormone-releasing hormone agonists or antagonists | 2 | [
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NCT02769611 | ,,,19:32:chronic_disease,19:37:chronic_disease,48:85:chronic_disease,,,189:205:treatment,209:220:treatment, | NYHA Class III-IV heart failure (HF) confirmed left ventricular systolic dysfunction with left ventricular ejection fraction (LVEF) <40% as assessed by noninvasive imaging studies such as echocardiography or cardiac MRI within the last 6 months admitted with decompensated heart failure and almost ready for clinical dis... | 2 | [
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NCT02533674 | 23:25:treatment,, | Patients who have had RT in more than 35% of the bone marrow | 2 | [
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NCT02213575 | 135:146:treatment, | unwilling to discontinue vitamin or supplements, including probiotics, potentially affecting gut microbiota (vitamins/supplements and medications that possibly affect the gut microbiota should be discontinued for at least 2wks prior to stool collection) | 2 | [
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NCT01964404 | 14:30:chronic_disease | History of a seizure disorder | 2 | [
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NCT02851472 | ,24:39:chronic_disease | Hypotensive for age or active bleeding | 2 | [
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NCT03093272 | 1:37:cancer | Castration-resistant prostate cancer | 2 | [
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NCT01897259 | ,133:145:chronic_disease | treatment by a health care profession (MD, physicians assistnat, therapist, or nurse practitioner) within the previous 6 months for tennis elbow | 2 | [
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NCT02616185 | 8:46:treatment,53:65:treatment,67:78:treatment,140:144:cancer | Failed prior therapy with a secondary hormone (e.g. enzalutamide, abiraterone) with documented progressive disease (post-secondary hormone CRPC) | 2 | [
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NCT02307058 | 15:25:chronic_disease | Subjects with T3 disease based on digital rectal exam (DRE) | 2 | [
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NCT02391402 | 14:18:chronic_disease | Diagnosis of PTSD based on the Clinician Administered PTSD Scale | 2 | [
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NCT02148796 | 54:60:chronic_disease | Participants may not have a physician's diagnosis of asthma | 2 | [
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NCT03016130 | 1:30:treatment | Allogeneic or autologous HSCT for any indication | 2 | [
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NCT02478255 | 30:41:treatment, | Patient scheduled to undergo thoracic RT at Duke University to a dose of at least 20 Gy | 2 | [
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NCT02336451 | 27:43:cancer,49:54:cancer,69:92:treatment,113:142:cancer | Patients must have active brain metastases from NSCLC, confirmed by Gadolinium-enhanced MRI without concomitant leptomeningeal carcinomatosis | 2 | [
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NCT02413047 | 16:26:chronic_disease,30:55:chronic_disease,63:95:chronic_disease,97:141:chronic_disease,143:164:treatment | Any identified congenital or acquired immunodeficiency (e.g., common variable immunodeficiency, human immunodeficiency virus [HIV] infection, organ transplantation) | 2 | [
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NCT02515110 | 12:57:treatment | History of ipsilateral or contralateral axillary surgery for any condition | 2 | [
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NCT03124355 | 37:57:chronic_disease,65:76:chronic_disease,78:89:treatment | Medical conditions that can explain postural tachycardia (e.g., dehydration, medications) | 2 | [
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NCT02308202 | 66:80:treatment,82:92:treatment,94:99:treatment,101:108:treatment,113:138:treatment | Have evidence of untreated or unstable medical illness including neuroendocrine, autoimmune, renal, hepatic, or active infectious disease | 2 | [
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NCT02593110 | 1:19:treatment, | orthopedic surgery during the past 3 months | 2 | [
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NCT02912572 | ,62:70:treatment, | Participant must not be pregnant or breastfeeding given that avelumab is an agent with unknown effects in pregnancy and breastfeeding and the potential for teratogenesis | 2 | [
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NCT02169739 | 10:24:chronic_disease, | Clinical lacunar stroke syndrome within the past 6 months | 2 | [
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NCT03035799 | 14:29:chronic_disease, | Uncontrolled thyroid disease as indicated by an abnormal thyroid stimulating hormone (TSH) level | 2 | [
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NCT01644591 | 50:60:allergy_name | Patients are excluded if there is any history of gadolinium allergy | 2 | [
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NCT02317991 | ,30:64:treatment | Patients must have < Grade 2 pre-existing peripheral neuropathy (per National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE] v 4.03) | 2 | [
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NCT03058146 | 12:33:chronic_disease,35:56:chronic_disease,58:64:chronic_disease | History of major vascular events (myocardial infarction, stroke, etc) | 2 | [
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NCT01799538 | 14:17:chronic_disease | Diagnosis of LAM | 2 | [
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NCT03112720 | 29:38:allergy_name | Subjects with an allergy to lidocaine | 2 | [
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NCT02350764 | ,,87:98:treatment, | Exception is made for patients with EGFR or ALK re-arrangements who must have stopped TKI therapy at least 7 days prior to C1D1 | 2 | [
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NCT02133573 | 17:29:treatment, | Maternal use of progesterone within 30 days of enrollment | 2 | [
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NCT01553071 | 35:42:treatment,44:53:treatment,84:100:cancer,124:146:treatment,,178:194:treatment | patients with previously treated (surgery, radiation or both), clinically inactive brain metastases, who have not received corticosteroid therapy within three weeks of starting protocol therapy | 2 | [
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NCT02361554 | 28:41:chronic_disease | Subject has a diagnosis of schizophrenia as determined by a review of medical records, discussion with referring psychiatrist as well as the Structured Clinical Interview for DSM-IV (SCID-IV) | 2 | [
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NCT01989585 | 23:36:treatment,38:50:treatment,54:66:treatment,,109:119:treatment,124:158:treatment,196:223:treatment,240:256:treatment,261:276:treatment,,325:335:treatment,343:353:treatment,355:376:treatment,,460:469:treatment,471:480:treatment, | Patients who have had immunotherapy, chemotherapy or radiotherapy within 14 days prior to the first dose of navitoclax, or prior systemic anti-cancer therapy (chemotherapy with delayed toxicity, extensive radiation therapy, immunotherapy, biologic therapy, or vaccine therapy) within the last 3 weeks prior to first dose... | 2 | [
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NCT02350764 | 35:63:treatment,84:93:treatment,98:122:treatment | Patients may not have intervening systemic anti-cancer therapy between the time of resection and treatment with nivolumab | 2 | [
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NCT02562755 | 1:36:chronic_disease,54:65:treatment,69:77:treatment | significant coronary artery disease (e.g., requiring angioplasty or stenting) | 2 | [
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NCT01421810 | 1:8:chronic_disease,37:53:chronic_disease,60:81:chronic_disease | Obesity associated with a diagnosed genetic syndrome (e.g. Prader-Willi syndrome) | 2 | [
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NCT01538966 | 116:143:treatment | The patient has had appropriate dynamic testing of the pituitary axis and, if applicable, is receiving appropriate hormone replacement therapy | 2 | [
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NCT02366754 | 6:33:treatment,37:50:treatment,52:68:treatment,72:88:treatment | Have implanted cardiac pacemaker or defibrillator, cochlear implant or nerve stimulator | 2 | [
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NCT00969111 | 8:20:treatment,24:36:treatment,91:100:treatment | Taking Saw Palmetto or methotrexate and unable or unwilling to discontinue its use during radiation | 2 | [
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NCT02810704 | 137:144:treatment,146:154:treatment,159:170:treatment | Concurrently enrolled in another active interventional clinical trial testing a drug or intervention known or believed to interact with aspirin, warfarin, or rivaroxaban | 2 | [
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NCT00632853 | 79:109:cancer,121:138:cancer,140:181:cancer,187:226:cancer | Limited-stage disease patients with disease restricted to one hemithorax with regional lymph node metastases, including ipsilateral hilar, ipsilateral and contralateral mediastinal, and ipsilateral supraclavicular lymph nodes | 2 | [
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NCT02393794 | 26:45:treatment,56:68:treatment,70:83:treatment,85:93:treatment,95:111:treatment,120:143:treatment | Subject has received any anti-cancer therapy including chemotherapy, immunotherapy, biologic, targeted therapy, or any investigational therapy | 2 | [
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NCT01871727 | 8:18:cancer,31:35:cancer,58:102:cancer,108:125:cancer,108:139:cancer, | Active malignancy (except for CTCL, definitively treated basal or squamous cell carcinoma of the skin, and carcinoma in-situ of the cervix) within the past 24 months | 2 | [
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NCT02278315 | 18:21:chronic_disease,23:34:chronic_disease,38:49:chronic_disease | Known history of HIV, hepatitis C or hepatitis B infection | 2 | [
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NCT02323126 | 25:42:treatment,59:69:treatment,,129:145:treatment,153:165:treatment | require emergent use of systemic steroids, chronic use of prednisone (greater than 10mg or an equivalent steroid dose daily) or emergent surgery and/or radiotherapy | 2 | [
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NCT02547662 | 7:36:chronic_disease,40:52:treatment,115:123:treatment | Known gastrointestinal (GI) disease or GI procedure that could interfere with the oral absorption or tolerance of ixazomib including difficulty swallowing | 2 | [
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NCT02851914 | 1:11:chronic_disease | Depression diagnosis by mental health provider | 2 | [
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NCT03181867 | 41:62:chronic_disease | Subjects with any coexisting medical or psychiatric condition that is likely to interfere with study procedures and/or results | 2 | [
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NCT02818972 | 47:73:chronic_disease,85:106:chronic_disease,118:141:chronic_disease,150:174:chronic_disease,176:182:chronic_disease,190:216:chronic_disease,241:258:chronic_disease,270:283:chronic_disease | Subjects with disease, for example: suspected connective tissue disorder, specified coagulation disorders, specified coronary artery disease, severe congestive heart failure, stroke and/or Myocardial Infarction (MI) as specified, specified pulmonary disease, specified renal failure | 2 | [
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NCT02807272 | 1:25:cancer | non-melanoma skin cancer | 2 | [
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NCT01474889 | 16:45:treatment,68:94:treatment,107:133:treatment,137:184:treatment,,,273:308:treatment,, | Involvement in intensive diabetes management defined as the use of basal-bolus insulin analog delivery by multi-dose injection (MDI) or continuous subcutaneous insulin infusion (CSII) together with self-monitoring of blood glucose values four or more times daily, without continuous glucose monitoring (CGM), under the d... | 2 | [
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NCT03042689 | 1:31:chronic_disease | Active coronary artery disease | 2 | [
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NCT02562430 | 27:41:treatment | Only one failed one prior antidepressant in the current episode | 2 | [
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NCT00291525 | ,17:45:treatment | Women receiving estrogen replacement therapy | 2 | [
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NCT03158519 | 1:14:chronic_disease | schizophrenia | 2 | [
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NCT02466971 | ,,43:52:treatment | Creatinine =< 1.5 mg/dL to receive weekly cisplatin | 2 | [
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NCT03122912 | 10:15:treatment,44:51:treatment,79:85:treatment, | Frequent NSAID use (not including low dose aspirin) and not willing to go off NSAIDS for 3 weeks prior to enrollment and to end of study | 2 | [
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NCT02219711 | 28:50:cancer | Metastatic or unresectable solid tumor malignancy | 2 | [
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NCT03078504 | 1:20:chronic_disease | unstable arrhythmia | 2 | [
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NCT02272998 | 31:57:chronic_disease,59:65:chronic_disease,67:98:chronic_disease,100:115:chronic_disease,119:146:chronic_disease | any patient with a history of myocardial infarction (MI), stroke, transient ischemic attack (TIA), unstable angina or peripheral vascular disease will not be eligible | 2 | [
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NCT02133898 | 14:39:chronic_disease, | Diagnosis of Major Depressive Disorder based on Structured Clinical Interview for DSM-IV (SCID) | 2 | [
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NCT02101736 | 1:17:cancer,19:58:cancer,69:79:cancer,90:99:treatment, | Malignant glioma, malignant peripheral nerve sheath tumor, or other malignancy requiring treatment in the last 12 months | 2 | [
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NCT02469857 | 1:36:chronic_disease | Idiopathic Thrombocytopenia Purpura | 2 | [
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NCT01877382 | 59:70:cancer,74:82:cancer,126:144:treatment | Has a histologically or cytologically documented advanced solid tumor or lymphoma that has relapsed from or is refractory to standard treatment | 2 | [
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NCT02191098 | ,,,51:64:chronic_disease,81:109:chronic_disease,86:108:chronic_disease,186:205:chronic_disease | NYHA (New York Heart Association) Class III or IV heart failure, uncontrollable supraventricular arrhythmias, any history of a ventricular arrhythmia, or other clinical signs of severe cardiac dysfunction | 2 | [
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NCT02950337 | 1:46:chronic_disease | severely symptomatic congestive heart failure | 2 | [
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NCT02128906 | 23:32:cancer | poorly differentiated carcinoma of the oropharynx, larynx | 2 | [
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