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NCT02750319 | 8:25:chronic_disease | not in cardiogenic shock | 2 | [
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NCT01589263 | ,45:90:treatment | This decision can be based on PSA velocity, previous TRUS (transrectal ultrasound) biopsy, percent free PSA, or other clinical estimations in keeping with sound urologic care | 2 | [
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NCT02216227 | 25:34:allergy_name | Documented allergies to mupirocin | 2 | [
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NCT01967823 | 38:60:treatment | Patients who are receiving any other investigational agents | 2 | [
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NCT02366871 | 21:39:chronic_disease | Known or documented bleeding disorders | 2 | [
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NCT02872935 | 23:44:chronic_disease | Any other physical or psychiatric condition that may impair their ability to cooperate with study data collection | 2 | [
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NCT02484300 | 12:23:treatment | Use of any medications that may affect sleep or breathing | 2 | [
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NCT02389309 | 28:52:treatment,54:65:treatment,67:89:treatment,122:130:treatment,194:207:treatment,,343:352:treatment | Inducers and Inhibitors of cytochrome P450 family 3, subfamily A, polypeptide 4 (CYP3A4): patients required to be on any CYP3A4/5 inhibitors or inducers will be excluded (with the exception of dexamethasone, but all efforts should be made to reduce the dose of dexamethasone); patients must discontinue drug at least 7 d... | 2 | [
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NCT03016351 | 13:26:chronic_disease,, | Presence of renal disease with a creatinine > 1.5mg/dL | 2 | [
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NCT02913404 | 76:102:treatment | Subjects will be of generally good health and will have decided to undergo ACL reconstruction surgery and agreed to participate in the study (following informed consent procedures) | 2 | [
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NCT02365467 | 16:65:chronic_disease | Subject has an acute dissection of the descending thoracic aorta | 2 | [
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NCT02493257 | 1:23:chronic_disease | Chronic rhinosinusitis | 2 | [
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NCT02274116 | 11:32:chronic_disease | recurrent autonomic dysreflexia | 2 | [
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NCT01993810 | 1:28:treatment,43:49:cancer,,76:98:treatment,,124:140:treatment | Prior systemic chemotherapy for the study cancer, if more than 4 cycles of induction chemotherapy or more than 6 months of targeted therapy | 2 | [
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NCT01883076 | 49:52:chronic_disease,54:65:chronic_disease,71:82:chronic_disease | Mother's serology test results are negative for HIV, Hepatitis B, and Hepatitis C | 2 | [
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NCT01970345 | 25:49:chronic_disease | Meet DSM-5 criteria for Autism Spectrum Disorder confirmed by the Autism Diagnostic Interview-Revised (ADI-R) | 2 | [
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NCT01349101 | 15:18:cancer | patients with MDS | 2 | [
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NCT00734877 | 43:45:cancer | Patients must have newly diagnosed active MM requiring treatment | 2 | [
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NCT02477839 | 25:41:chronic_disease | Subject has experienced febrile seizures exclusively | 2 | [
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NCT02867696 | 17:35:chronic_disease,37:43:chronic_disease,58:68:chronic_disease,114:140:chronic_disease,142:173:treatment,177:188:treatment,196:217:chronic_disease,244:267:treatment | Reports current congestive failure, angina, uncontrolled arrhythmia, symptoms indicative of increased risk of an acute cardiovascular event, coronary artery bypass grafting or angioplasty, prior myocardial infarction, and conditions requiring anticoagulation therapy (deep vein thrombosis) | 2 | [
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NCT02927847 | 35:63:treatment | presence of contraindications for nicotine replacement therapy | 2 | [
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NCT02416102 | 12:33:chronic_disease | History of renal artery stenosis | 2 | [
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NCT01988246 | 28:47:treatment | Patients who have received corneal transplants in the study eye | 2 | [
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NCT03115398 | 14:46:cancer,48:68:cancer,70:74:cancer,76:98:cancer,103:117:cancer | Diagnosis of invasive malignancy of the brain, head and neck region, lung, gastrointestinal tract, or uterine cervix | 2 | [
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NCT03168347 | 40:59:treatment | Currently or previously managed with a biologic medication | 2 | [
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NCT00432094 | 26:31:cancer,74:93:chronic_disease,112:122:treatment | Patients with increasing tumor markers only (i.e. no imaging evidence of progressive disease) are eligible for transplant | 2 | [
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NCT02903446 | 7:20:chronic_disease | Other bone diseases which affect bone metabolism | 2 | [
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NCT02451488 | ,72:78:treatment | All WOCBP must have a negative pregnancy test prior to first receiving GM-CSF | 2 | [
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NCT02620579 | 21:44:treatment | previous history of upper-extremity surgery | 2 | [
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NCT02516670 | 16:38:chronic_disease | Has history of calcium oxalate stones | 2 | [
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NCT03004807 | 14:35:chronic_disease,, | Uncontrolled stage II hypertension (blood pressure above 159/99 mm Hg) | 2 | [
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NCT02479230 | 32:50:cancer | Patients must have evidence of metastatic disease measurable by Response Evaluation Criteria in Solid Tumors (RECIST) criteria or non-measurable lytic or mixed (lytic + blastic) bone lesions in the absence of measurable disease | 2 | [
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NCT02576431 | 47:89:treatment | Prior progression while receiving approved or investigational tyrosine kinase inhibitors targeting TRK | 2 | [
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NCT01730118 | 15:22:cancer,24:32:cancer,34:39:cancer,41:48:cancer,49:74:cancer,76:95:cancer,97:107:cancer,109:116:cancer,118:139:cancer,144:170:cancer,180:192:cancer,,, | Patients with ovarian, cervical, colon, gastric/gastroesophageal junction, non-small cell lung, renal cell, bladder, malignant soft tissue and bone tumor prostate cancer or other solid tumors that is known to be HER2 1+, 2+ or 3+ by IHC OR have a Vysis FISH result greater than or equal to 1.8 | 2 | [
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NCT02548104 | 1:19:treatment | General anesthesia | 2 | [
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NCT01969643 | 18:39:cancer, | Combination Arm: HER2-positive disease and received at least 2 prior cytotoxic regimens in the incurable, unresectable, LA/MBC setting (not enrolling new patients) | 2 | [
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NCT01841333 | 8:27:chronic_disease, | Active cardiac arrhythmias with rapid ventricular response (defined as heart rate greater than 100 beats/minute) | 2 | [
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NCT02382419 | 42:60:allergy_name | Any known allergy or hypersensitivity to vaginal lubricants or any component of study product | 2 | [
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NCT02304458 | ,48:67:chronic_disease | Serum lipase =< ULN at baseline; patients with glucose intolerance should be on a stable regimen and be monitored | 2 | [
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NCT02509507 | 30:69:cancer,74:98:cancer,106:120:cancer,158:177:cancer,187:192:cancer,194:197:cancer,212:220:cancer | Subjects must either have no central nervous system (CNS) metastasis, or carcinomatous meningitis, or if CNS metastasis is present, must have stable treated cerebral metastases from BC, NSCLC, RCC, CRC, GEC, or melanoma | 2 | [
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NCT01754857 | ,43:55:treatment | at least 28 days before she starts taking lenalidomide | 2 | [
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NCT02797795 | 5:17:treatment,19:48:treatment,50:81:treatment,83:108:treatment,,138:148:treatment,230:253:treatment, | Any chemotherapy, immunomodulatory drug therapy, antineoplastic hormonal therapy, immunosuppressive therapy, corticosteroids > 20 mg/day prednisone or equivalent (unless administered to prevent contrast material reactions during radiographic procedures), or growth factor treatment (e.g., erythropoietin) within 14 days ... | 2 | [
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NCT01968109 | 1:44:cancer,48:60:cancer,66:80:cancer | Primary central nervous system (CNS) tumors or solid tumors with CNS metastases as the only site of active disease | 2 | [
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NCT01591356 | 45:106:allergy_name,108:117:allergy_name,122:146:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to DOPC, Magnevist, or fluorodeoxyglucose (FDG) | 2 | [
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NCT02203552 | 25:57:treatment,58:73:treatment,103:122:treatment,136:145:treatment,157:171:chronic_disease | Any contraindication to magnetic resonance imaging (MRI)/PET examination including but not limited to ferromagnetic metal in the body, pacemaker, or severe claustrophobia | 2 | [
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NCT01812174 | 21:51:chronic_disease | Patients who have a noncardiac progressive disease, which in the investigator's experience produces an unacceptable increased risk to the patient | 2 | [
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NCT02166905 | 1:18:chronic_disease | Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study | 2 | [
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NCT01925131 | 63:66:cancer,91:100:treatment,,178:204:treatment | Patients known to have Philadelphia chromosome positive (Ph+) ALL must have either failed treatment or been intolerant to treatment with at least two second or third generation tyrosine kinase inhibitors | 2 | [
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NCT02427841 | 18:21:chronic_disease,25:27:chronic_disease,96:117:treatment | Occlusion of the SMV or PV with insufficient normal vein above and below with which to perform venous reconstruction | 2 | [
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NCT02099058 | 17:42:treatment | Subjects in the combination therapy Arm E | 2 | [
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NCT02349867 | 13:31:cancer | Evidence of metastatic disease | 2 | [
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NCT02391402 | 24:35:chronic_disease,78:94:chronic_disease,99:118:chronic_disease,159:169:treatment | Individuals with other psychiatric diagnoses will not be excluded except for bipolar disorder and psychotic disorders (requirement to refrain from additional treatments might be harmful) | 2 | [
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NCT02859142 | 9:26:chronic_disease, | Current suicidal ideation (past 6 months) | 2 | [
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NCT03134274 | 6:21:chronic_disease | Have impaired vision that prevents them from reading instructions | 2 | [
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NCT02413970 | 54:58:treatment | Subjects who have been prescribed, but refuse to try CPAP would be considered intolerant | 2 | [
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NCT02488967 | 26:36:treatment,106:120:cancer,125:156:cancer | For patients who undergo lumpectomy, the margins of the resected specimen must be histologically free of invasive tumor and ductal carcinoma in situ (DCIS) as determined by the local pathologist | 2 | [
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NCT01928576 | 102:112:allergy_name,114:125:allergy_name,130:139:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to entinostat, azacitidine, or Nivolumab | 2 | [
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NCT02641093 | 1:12:chronic_disease | Hepatitis C | 2 | [
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NCT00670358 | 1:37:chronic_disease | Psychiatric illness/social situation that would preclude compliance with study requirements | 2 | [
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NCT02851303 | 41:54:treatment | Primary substance exposure in-utero was buprenorphine, or was not opioids | 2 | [
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NCT02392286 | 13:44:treatment, | Patients on systemic corticosteroid therapy currently or within the past 8 weeks | 2 | [
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NCT01050855 | 1:34:chronic_disease | Severe combined immune deficiency | 2 | [
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NCT01494662 | 27:39:treatment,43:55:treatment,67:89:treatment,, | Participants who have had chemotherapy or radiotherapy (including investigational agents) within 2 weeks prior to entering the study or those who have not recovered adequately from adverse events due to agents administered more than 4 weeks earlier | 2 | [
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NCT02128230 | 74:93:treatment | Patients must be either untreated or have not had more than one cycle of systemic MM therapy | 2 | [
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NCT01130077 | 17:35:cancer,40:58:cancer,72:84:treatment,92:109:treatment | Newly diagnosed high-grade gliomas* or brain stem gliomas who received chemotherapy during radiation therapy. Patients may not have received chemotherapy after radiation therapy was completed | 2 | [
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NCT02531880 | 25:48:treatment | On-going treatment with calcium-channel blocker | 2 | [
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NCT01920737 | 15:49:chronic_disease,53:56:cancer,86:107:treatment,113:130:treatment,138:162:treatment | Patients with central nervous system involvement by ALL are eligible and may receive concomitant treatment with radiation therapy and/or intrathecal chemotherapy in accordance with standard medical practice | 2 | [
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NCT03059407 | 39:54:chronic_disease | or concern for immune system function/infectious risk that could be worsened by animal exposure | 2 | [
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NCT02252432 | 57:68:allergy_name | Intolerance, allergy, or contraindication to use of any medications used in this study | 2 | [
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NCT02501733 | 19:33:chronic_disease | Patients that are morbidly obese | 2 | [
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NCT02036853 | 31:44:treatment | Concomitant administration of valproic acid | 2 | [
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NCT02844504 | 77:83:treatment,85:95:treatment,97:108:treatment,112:127:treatment | Current medication believed to affect cognitive/psychomotor function (i.e., opioid, analgesics, anxiolytics or antidepressants) | 2 | [
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NCT02213497 | 52:63:chronic_disease,65:70:chronic_disease,72:79:chronic_disease,84:102:chronic_disease | Patients must be surgical candidates with adequate hematologic, renal, hepatic and pulmonary function | 2 | [
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NCT02556606 | 72:83:chronic_disease,189:211:chronic_disease,229:241:chronic_disease,281:299:chronic_disease | Serious, unstable medical illnesses including respiratory [obstructive sleep apnea, or history of difficulty with airway management during previous anesthetics], cardiovascular [including ischemic heart disease and uncontrolled hypertension], and neurologic [including history of severe head injury] | 2 | [
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NCT02400255 | 13:28:chronic_disease,,,,79:94:chronic_disease,103:113:treatment | Significant cardiac disease (New York Heart Association classes III or IV) or unstable angina despite medication | 2 | [
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NCT02479906 | 44:75:chronic_disease | Any condition likely to be associated with increased intracranial pressure | 2 | [
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NCT02169739 | 1:19:chronic_disease | hemorrhagic stroke | 2 | [
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NCT03131960 | 13:25:chronic_disease | Significant sensory loss | 2 | [
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NCT02587403 | 21:51:treatment, | Participation in an investigational drug or device study that would impact the safety or scientific integrity of this study (in the opinion of the Investigator and with the approval of the Sponsor) within the past 6 weeks prior to enrollment into this trial | 2 | [
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NCT00703105 | 41:63:treatment | Patients may not be receiving any other investigational agents | 2 | [
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NCT02120222 | 1:20:chronic_disease | Serious psychiatric or medical conditions that could interfere with treatment | 2 | [
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NCT03016871 | 1:24:treatment | Prior radiation therapy is allowed | 2 | [
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NCT01897259 | 39:48:treatment,87:102:treatment,113:129:treatment, | pain over the lateral epicondyle (via palpation over the lateral epicondyle, resisted wrist extension, resisted finger extension of the middle finger) for less than six-months duration prior to enrollment | 2 | [
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