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NCT02905370 | 1:10:chronic_disease | Pneumonia | 2 | [
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NCT02479620 | 9:36:treatment | Planned major index limb amputation | 2 | [
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NCT01753986 | 18:53:treatment | Participation in Batterer Intervention Program in RI | 2 | [
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NCT03072381 | 37:53:treatment | self-reported failure of supervised physical therapy | 2 | [
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NCT02903446 | 12:27:chronic_disease | History of Addison disease | 2 | [
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NCT01804465 | 1:24:treatment, | Prior radiation therapy must be completed ≥ 4 weeks prior to enrollment and the patient must have recovered from all toxicity | 2 | [
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NCT02468778 | 20:48:chronic_disease | intervention of an unprotected left main artery | 2 | [
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NCT01822522 | ,,141:156:treatment | The participant has not recovered to baseline or Common Terminology Criteria for Adverse Events (CTCAE) =< grade 1 from toxicity due to all prior therapies | 2 | [
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NCT02089607 | 18:25:treatment,74:80:chronic_disease,85:113:chronic_disease,130:179:treatment,183:206:treatment | Examples include therapy directed to reduce rates of spinal cord injury, stroke and contrast-induced nephropathy associated with implantation of fenestrated-branched stent-grafts or advanced imaging trials designed to reduce radiation exposure during repair | 2 | [
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NCT01954173 | 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 at the time of registration | 2 | [
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NCT02417701 | 84:93:chronic_disease | Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection | 2 | [
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NCT02489019 | 24:46:treatment | Patients scheduled for cardiovascular surgery | 2 | [
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NCT02582905 | ,,,,141:158:chronic_disease | High risk for suicide defined as > 1 attempt in past 12 months that required medical attention, any attempt in the past 3 months or current suicidal ideation with plan and intent such that outpatient care is precluded | 2 | [
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NCT01734512 | 35:41:cancer | Patients with primary spinal cord tumors | 2 | [
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NCT02667418 | 1:11:treatment | vancomycin | 2 | [
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NCT02487797 | 12:53:treatment | History of prior cesarean section or uterine surgery | 2 | [
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NCT02465541 | ,15:20:chronic_disease, | Overweight or obese (> 25 kg/m^2) | 2 | [
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NCT02004275 | 18:37:chronic_disease,43:54:treatment,58:80:treatment | Prior history of erythema multiforme with thalidomide or lenalidomide treatment | 2 | [
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NCT02425566 | 1:6:chronic_disease | obese | 2 | [
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NCT02451215 | 1:14:cancer | Ganglioglioma | 2 | [
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NCT02551679 | 1:14:chronic_disease | Renal failure | 2 | [
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NCT02937402 | 1:20:chronic_disease,,50:74:treatment,78:91:treatment,95:117:treatment, | Respiratory failure requiring greater than 6 Lpm supplemental oxygen (O2) by nasal cannula or mechanical ventilation within the past six weeks | 2 | [
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NCT01962415 | 1:17:chronic_disease | Leukodystrophies | 2 | [
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NCT01174121 | 15:27:cancer,56:63:treatment,65:82:treatment,88:100:treatment,111:125:cancer,119:125:cancer,138:147:treatment | Patients with glioblastoma must have received standard surgery, radiation therapy, and chemotherapy for their primary tumors and require resection of their tumors for palliative or other clinical indication | 2 | [
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NCT02130687 | ,,49:61:treatment | 2-hour plasma glucose ≥200 mg/dL following 75gr oral glucose load | 2 | [
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NCT02413047 | 5:11:cancer, | Any cancer within the past 5 years | 2 | [
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NCT01701986 | ,,166:188:treatment | Pregnancy (positive beta human chorionic gonadotropin [HCG] test in a woman with child bearing potential defined as not post-menopausal for 12 months or no previous surgical sterilization) or currently breast-feeding | 2 | [
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NCT02172651 | ,10:37:treatment,, | women on hormone replacement therapy with documented serum follicle stimulating hormone level >35 mIU/mL) | 2 | [
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NCT03188042 | 1:21:chronic_disease, | Visual field defects present for at least 6 months | 2 | [
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NCT03072238 | 12:31:chronic_disease | measurable soft tissue disease by computed tomography (CT) | 2 | [
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NCT03135522 | 12:24:chronic_disease | History of lung disease | 2 | [
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NCT02522468 | 1:20:treatment | Breast-conservation candidate | 2 | [
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NCT02092324 | 34:68:chronic_disease,72:98:chronic_disease,102:103:chronic_disease | Subjects with known diagnosis of human immunodeficiency virus (HIV) or chronic active Hepatitis B or C | 2 | [
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NCT01415752 | 49:69:chronic_disease,99:106:treatment,,,129:144:treatment | Patients on Arms G and H without a history of a thromboembolic event are required to take a daily aspirin (81 mg or 325 mg) for DVT prophylaxis | 2 | [
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NCT02273375 | 7:19:cancer,,102:111:treatment,223:233:cancer | other malignancies curatively treated with no evidence of disease for ≥ 5 years following the end of treatment and which, in the opinion of the treating physician, do not have a substantial risk of recurrence of the prior malignancy | 2 | [
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NCT02685358 | 7:27:chronic_disease | gross cognitive impairment | 2 | [
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NCT01865162 | 1:20:cancer,22:45:cancer,47:50:cancer | Astrocytoma grade 4 (glioblastoma multiforme, GBM, histologically confirmed, WHO criteria) | 2 | [
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NCT02724540 | 1:10:treatment | sedatives | 2 | [
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NCT02272218 | 38:49:treatment,50:66:treatment,103:110:treatment,115:130:treatment | has not yet tried to treat pain with oral NSAIDs/COX-2 inhibitors (unless medical contraindications), Tylenol, or topical therapy | 2 | [
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NCT02425904 | 28:80:treatment,156:162:chronic_disease,164:173:chronic_disease,184:193:chronic_disease,208:234:chronic_disease,251:260:chronic_disease | Patients with a history of prior hematopoietic stem cell transplantation (HSCT), elevated conjugated serum bilirubin at study entry, uncontrolled systemic fungal, bacterial, or other infection, a history of hepatitis B or C infection or a history of cirrhosis | 2 | [
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NCT02762006 | 13:22:treatment,28:41:treatment,50:60:cancer,71:79:cancer,81:99:treatment,101:117:chronic_disease | No previous treatment with immunotherapy for any malignancy including cytokine, anti-tumor vaccine, T-cell activator, co-stimulator or immune checkpoint inhibitor | 2 | [
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NCT02277548 | ,,,44:57:chronic_disease | New York Heart Association class III or IV heart failure | 2 | [
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NCT02461927 | 42:50:allergy_name,52:61:allergy_name,63:73:allergy_name,78:87:allergy_name | Unstable medical condition or allergy to ketamine, midazolam, naltrexone, or lorazepam---clinically determined by a physician | 2 | [
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NCT03042689 | 22:28:cancer, | Subjects surviving a cancer that was curatively treated and without evidence of disease for more than 3 years before registration are allowed | 2 | [
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NCT02153229 | 15:24:chronic_disease,48:57:allergy_name,61:85:allergy_name | Patients with porphyria or hypersensitivity to porphyrin or porphyrin-like compounds | 2 | [
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NCT01622868 | 7:11:treatment | Prior WBRT | 2 | [
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NCT02056470 | 1:21:chronic_disease | renal osteodystrophy | 2 | [
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NCT01409161 | ,48:71:treatment, | Fridericia corrected QT (QTcF) interval on the electrocardiogram (EKG) greater than 480 milliseconds | 2 | [
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NCT03121352 | 45:116:allergy_name,118:129:allergy_name,131:144:allergy_name,149:161:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to nab-paclitaxel, carboplatin, pembrolizumab, or other agents used in this study | 2 | [
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NCT02924402 | 22:54:allergy_name | Known intolerance to CD20 monoclonal antibody therapy | 2 | [
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NCT03022292 | 5:39:treatment,85:146:treatment,148:174:treatment,176:193:treatment,195:219:treatment,221:247:treatment,249:272:treatment,288:336:treatment | Any prior treatment of neovascular AMD in the eye proposed for enrollment including previous anti-vascular endothelial factor (anti-VEGF) therapy, photodynamic therapy (PDT), radiation therapy, corticosteroid treatment, surgical treatment for CNV, thermal laser treatment, and any other prior intravitreal treatment for ... | 2 | [
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NCT02354703 | 51:58:treatment,60:67:treatment,69:81:treatment,83:95:treatment,100:115:treatment,174:184:treatment | At the Screen Visit, the subject's urine contains opiates, cocaine, amphetamines, barbiturates, or benzodiazepines that cannot be explained by appropriate use of prescribed medication | 2 | [
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NCT02431806 | 33:48:chronic_disease,60:63:chronic_disease,93:102:treatment | DSM-IV-TR-based diagnosis of an axis I disorder other than MDD that is the primary focus of treatment | 2 | [
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NCT02836574 | 1:24:treatment,9:24:treatment,29:61:treatment,,182:188:chronic_disease | inhaled corticosteroids and chronic low-dose corticosteroids (less than or equal to 7.5 mg per day) are permitted as are brief pulsed corticosteroids for intermittent symptoms (eg, asthma) | 2 | [
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NCT01990495 | ,,,140:153:chronic_disease | Subjects will be required to be in the peak VO2 range of 10 to 20 ml/kg/min, equivalent to moderate functional impairment in patients with heart failure | 2 | [
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NCT03001882 | 27:75:cancer,84:117:treatment,127:142:treatment,159:177:cancer | Histologically confirmed, stage IV or recurrent non-small cell lung cancer with no prior systemic anticancer therapy given as primary therapy for advanced or metastatic disease | 2 | [
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NCT01787682 | 54:81:chronic_disease,,, | Clinically stable condition and not suffering from a respiratory tract infection or exacerbation of their disease (defined as a combination of increased cough, sputum purulence, shortness of breath, systemic symptoms such as fever, and a decrease in FEV1 > 10% compared with values when clinically stable in the precedin... | 2 | [
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NCT03071393 | 18:39:chronic_disease | severe recurrent autonomic dysreflexia | 2 | [
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NCT02849639 | 1:30:chronic_disease | Blockage of the urinary tract | 2 | [
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NCT02493257 | 1:31:treatment | Radiation to the head and neck | 2 | [
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NCT02453373 | 12:35:chronic_disease | history of cold agglutinin disease | 2 | [
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NCT02495168 | 24:42:treatment,44:47:treatment,52:57:treatment | Willing to discontinue asthma medications (ICS and LABAs) during the Run-in Period and for the remainder of the study | 2 | [
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NCT02688647 | 41:48:chronic_disease | Acute or chronic impairment (other than dyspnea) limiting the ability to comply with study requirements (eg, pulmonary function tests) | 2 | [
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NCT02240498 | 63:74:chronic_disease,76:87:chronic_disease,102:114:chronic_disease | All patients with clinical symptoms (ex: fever, chills, pain, tachycardia, hypotension), laboratory (leukocytosis) and radiologic findings (thick walled, rim-enhancing collection with gas bubbles or air-fluid levels) compatible with an abscess that requires image-guided percutaneous drainage | 2 | [
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NCT02050113 | 12:22:treatment,, | For use of Zenith TX2: diameter >38 mm or <24 mm (for proximal and distal neck diameter) | 2 | [
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NCT02918864 | 8:24:chronic_disease | simple febrile seizures | 2 | [
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NCT02085941 | 19:25:cancer | Participants with tumors involving the optic chiasm, brain, or spinal cord | 2 | [
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NCT02519452 | 6:27:treatment,78:87:treatment,89:128:treatment,137:156:treatment,158:170:treatment,172:187:treatment | Each prior line of therapy may consist of one or more agents and may include induction, hematopoietic stem cell transplantation, and/or maintenance therapy. Radiotherapy, bisphosphonates | 2 | [
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NCT02876302 | 32:39:cancer,,103:126:cancer,132:181:cancer | Individuals with the following cancers are eligible if diagnosed and treated within the past 3 years: cervical cancer in situ, and basal cell or squamous cell carcinoma of the skin | 2 | [
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NCT02271100 | 22:41:allergy_name | Contraindications to neuraxial analgesia | 2 | [
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NCT02101853 | 60:88:treatment | No waiting period for patients who relapse while receiving standard maintenance therapy | 2 | [
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NCT02361554 | 34:53:treatment,69:78:treatment,,,169:183:treatment, | Adequate trials of two different antipsychotic drugs (not including clozapine) belonging to different classes of at least 12 weeks equivalent to at least 500 mg/day of chlorpromazine within the previous 5 years | 2 | [
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NCT02583893 | 53:75:cancer | Patients must have histologic evidence of high risk acute myeloid leukemia | 2 | [
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NCT02834403 | 12:33:chronic_disease,35:41:chronic_disease,43:65:chronic_disease,70:104:chronic_disease, | History of myocardial infarction, stroke, ventricular arrhythmia, or symptomatic conduction abnormality within the past 12 months | 2 | [
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NCT02963831 | 1:40:treatment,,110:130:treatment,132:184:treatment,186:224:treatment,228:272:treatment | Treatment with an investigational agent within 4 weeks of starting study treatment or prior treatment with a checkpoint inhibitor (cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death protein 1 (PD-1) or programmed death ligand 1 (PD-L1) antibodies) | 2 | [
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NCT02141919 | 36:64:treatment,80:83:treatment,87:99:treatment | Subjects may not have received any treatment for the renal mass before such as RFA or cryoablation | 2 | [
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NCT02357784 | 7:37:chronic_disease | has > Stage II pelvic organ prolapse | 2 | [
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NCT02688309 | 20:66:treatment, | Previous use of an anti-Vascular Endothelial Growth Factor (VEGF) drug within 1 month of study entry | 2 | [
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NCT03078907 | 5:20:treatment, | Any hospitalization during the last 30 days prior to screening | 2 | [
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NCT02408406 | 28:34:cancer | Malignant diagnosis in any cancer type at any stage | 2 | [
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NCT00673842 | 1:33:treatment | Cardiac Resynchronization device | 2 | [
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NCT02304458 | ,,,106:128:treatment, | Antibodies: >= 21 days must have elapsed from infusion of last dose of antibody, and toxicity related to prior antibody therapy must be recovered to grade =< 1 | 2 | [
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NCT02360579 | 39:55:chronic_disease,65:112:chronic_disease,117:158:chronic_disease | Patients who have any form of primary immunodeficiency (such as severe combined immunodeficiency disease [SCID] and acquired immunodeficiency syndrome [AIDS]) | 2 | [
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NCT01059786 | 1:11:treatment, | cladribine for 6 months prior to study entry | 2 | [
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NCT02544880 | 1:16:treatment,34:47:treatment,55:67:treatment,105:114:treatment,118:142:cancer,144:154:cancer,156:167:cancer,171:177:cancer | Prior radiation, with or without prior surgery and/or chemotherapy, to the head and neck for definitive treatment of HNSCC of the oral cavity, oropharynx, hypopharynx or larynx with previously documented complete clinical or radiographic response to initial treatment | 2 | [
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