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NCT01787409 | 26:100:treatment | patients can begin their chemotherapy while awaiting vitamin D results and treatment arm assignment | 2 | [
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NCT02564744 | ,53:69:treatment,62:69:treatment,,116:137:treatment,,268:280:treatment,286:332:treatment | Participants who received at least only one line of previous therapy and achieved either complete response (CR) or partial response (PR) for at least 24 weeks (from the last day of the last cycle) after their first line of therapy, but are not eligible for high dose chemotherapy with autologous stem cell transplantatio... | 2 | [
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NCT02839759 | 14:35:treatment, | Prior use of hearing amplification within the past 10 years | 2 | [
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NCT00695214 | 34:42:treatment,56:72:treatment,76:92:treatment | Other contraindication to use of propofol (decision of anesthesiologist or otolaryngologist.) | 2 | [
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NCT02584647 | 1:4:chronic_disease,38:60:treatment,139:146:treatment | HIV-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with PLX3397 | 2 | [
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NCT02056873 | 39:62:chronic_disease,64:77:chronic_disease,79:93:chronic_disease,103:123:chronic_disease,125:146:chronic_disease,192:199:treatment | Severe medical co-morbidity including cardiovascular disorder, lung disorder, kidney disease, chronic neurological disease, hematological disease, or frailty that impacts tolerability of the surgery as judged by the screening physicians | 2 | [
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NCT02291523 | 12:22:chronic_disease,36:58:treatment,68:85:chronic_disease,87:96:chronic_disease | Concurrent infections that require anti-microbial therapy (such as abdominal abscess, pneumonia, etc… | 2 | [
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NCT02291848 | 28:38:treatment,42:55:treatment,,78:93:treatment | If patient has received an autologous or syngeneic SCT they must be >90 days post-transplant (Group A) | 2 | [
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NCT02167958 | 1:16:cancer | Acute Leukemias in 2nd or subsequent remission | 2 | [
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NCT02587962 | 1:32:treatment,34:44:treatment,46:56:treatment,58:68:treatment,73:130:treatment | Prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody | 2 | [
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NCT03182751 | 18:33:chronic_disease,35:57:chronic_disease,59:84:chronic_disease,86:110:chronic_disease,112:147:chronic_disease,149:167:chronic_disease | Known history of Factor V Leiden, protein C/S deficiency, prothrombin gene mutation, anti-thrombin deficiency, anti-phospholipid antibody syndrome, lupus anticoagulan | 2 | [
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NCT02589522 | ,,,61:64:treatment,71:94:chronic_disease,,,,154:194:treatment,247:251:treatment | Patients with 1-3 brain metastases, each < 3 cm by contrast MRI, with stable systemic disease and ECOG score of 0-2, who would otherwise be eligible for SRS/stereotactic radiation therapy (SRT) alone should not be enrolled into this study unless WBRT is recommended due to any medical reasons or logistic limitations as ... | 2 | [
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NCT02323100 | 16:36:treatment,38:58:treatment,81:115:treatment, | Current use of ivacaftor (Kalydeco), lumacaftor/ivacaftor combination, or other corrector or potentiator (Symdeko) less than 30 days from Screening | 2 | [
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NCT02615873 | 24:32:treatment | Has a good response to Levodopa in the opinion of the investigator | 2 | [
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NCT01993810 | 1:27:treatment,28:62:treatment,63:92:treatment, | Fludeoxyglucose F 18 (FDG)-positron emission tomography (PET)/computed tomography (CT) scan for staging within 60 days prior to registration | 2 | [
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NCT03079297 | 1:24:treatment,26:29:treatment,34:38:treatment,49:81:treatment | Vagus nerve stimulation, ECT, or rTMS, or other somatic antidepressant treatment during current episode | 2 | [
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NCT01220583 | 15:43:treatment,51:56:treatment,60:73:treatment,82:94:treatment | No concurrent hematopoietic growth factors (e.g., G-CSF or pegfilgrastim) during radiotherapy | 2 | [
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NCT00670358 | 19:28:chronic_disease | Ongoing or active infection | 2 | [
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NCT02695433 | 12:25:chronic_disease,27:38:chronic_disease,40:45:chronic_disease,47:63:chronic_disease,67:82:chronic_disease | History of heart disease, respiratory, renal, gastrointestinal or hepatic disease | 2 | [
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NCT02467478 | 12:18:cancer, | History of cancer within the past 5 years | 2 | [
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NCT02122081 | 11:42:treatment | Receiving supplementary continuous oxygen | 2 | [
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NCT01959204 | 80:94:chronic_disease,96:107:chronic_disease,109:114:chronic_disease,116:132:chronic_disease,134:145:chronic_disease,147:158:chronic_disease,160:169:chronic_disease,174:194:chronic_disease,198:217:chronic_disease | Has the presence or history of a clinically significant disorder involving the cardiovascular, respiratory, renal, gastrointestinal, immunologic, hematologic, endocrine, or neurologic system(s) or psychiatric disease (except for the condition for which the procedure is being performed) as determined by the clinical inv... | 2 | [
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NCT03018704 | 34:57:treatment | current regular treatment with a psychotropic medication, including medications that, when combined with alcohol, present a risk of overdose | 2 | [
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NCT03127722 | 36:65:treatment | Subjects who have had an attempted prior sterilization procedure | 2 | [
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NCT02343042 | 46:55:treatment | Prior exposure to a SINE compound, including selinexor | 2 | [
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NCT02585232 | 21:41:chronic_disease | Experiencing severe cognitive impairment that would impair their ability to communicate during an interview | 2 | [
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NCT03101566 | 12:28:treatment,,,82:92:treatment,144:162:chronic_disease | Inhaled or topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease | 2 | [
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NCT02423863 | 52:70:cancer, | Radiologically or visually measurable recurrent or metastatic disease that is measurable and at least 10mm in longest dimension | 2 | [
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NCT03109210 | 21:24:chronic_disease,, | have a diagnosis of OSA with an AHI > 5 on a diagnostic polysomnogram | 2 | [
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NCT01871454 | 71:81:cancer,87:99:treatment,101:122:treatment | A reasonable attempt should be made to make a pathologic diagnosis of malignancy (ie. bronchoscopy, CT guided lung biopsy) | 2 | [
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NCT03092635 | 16:32:cancer,82:90:treatment,94:118:treatment | Treated stable brain metastases are allowed, as long as patient does not require steroids or anti-seizure medications | 2 | [
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NCT02943590 | 20:32:treatment | Concomitant use of cyclosporine | 2 | [
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NCT01505569 | 1:14:cancer,44:64:cancer,141:152:cancer,182:215:treatment | Neuroblastoma (ICD-O morphology 9500/3) or ganglioneuroblastoma (nodular or intermixed) verified by histology or demonstration of clumps of tumor cells in bone marrow with elevated urinary catecholamine metabolites | 2 | [
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NCT02452203 | 30:47:chronic_disease | Participant endorses current suicidal ideation with intent or plan | 2 | [
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NCT02501473 | 12:30:treatment, | Received a live virus vaccine within 30 days of planned study start | 2 | [
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NCT02577406 | 84:96:treatment,100:133:treatment,154:164:treatment | Subjects with degenerative and toxic encephalopathies, especially after the use of methotrexate or treatment with ionizing radiation, should not receive cytarabine | 2 | [
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NCT02124772 | 1:14:treatment,44:50:cancer,52:83:cancer,89:116:cancer | Prior therapy: The subject's disease (i.e. cancer, neurofibromatosis type 1 [NF-1] with plexiform neurofibroma [PN] | 2 | [
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NCT03112720 | 37:52:treatment | Subjects already being treated with lidocaine patch or other vehicle for chronic pain | 2 | [
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NCT02056470 | 95:113:chronic_disease,115:120:chronic_disease,122:140:chronic_disease | Other significant disabling problems from the muscular-skeletal system than in the knees (i.e muscular dystrophy, polio, nueropathic joints) | 2 | [
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NCT01570816 | 1:22:chronic_disease | autoimmune deficiency | 2 | [
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NCT03113825 | 30:43:chronic_disease, | Hx of coronary events and/or heart failure within 1 year | 2 | [
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NCT01928576 | 39:59:treatment,68:86:treatment,115:134:treatment | Patients must be willing to undergo a pre-treatment biopsy, either core needle biopsy or equivalent amount or via excisional specimen | 2 | [
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NCT01688388 | 1:19:cancer | Distant metastases | 2 | [
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NCT01851369 | 34:46:treatment,48:65:treatment,70:86:treatment,,,,201:213:treatment,217:228:treatment,,317:327:treatment,,402:430:treatment,522:552:treatment | Patients must have completed any chemotherapy, radiation therapy, or biologic therapy greater than or equal to 4 weeks (or 5 half-lives, whichever is shorter) prior to entering the study (6 weeks for nitrosoureas or mitomycin C). Patients must be greater than or equal to 2 weeks since any prior administration of a stud... | 2 | [
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NCT02549833 | 53:59:cancer,75:86:cancer,88:105:cancer,110:126:cancer,191:200:treatment,237:243:treatment | must have newly diagnosed or recurrent WHO grade II glioma (defined as an astrocytoma, oligodendroglioma, or oligoastrocytoma) that is to be histologically confirmed by clinically indicated resection. If patients have already undergone biopsy and have pathological diagnosis of WHO grade II glioma, pathology must be rev... | 2 | [
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NCT02476786 | 20:30:cancer,,71:90:treatment,100:106:cancer | A history of other malignancy ≤ 5 years previous which would preclude endocrine treatment of their cancer | 2 | [
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NCT02479451 | 28:40:allergy_name | Prior allergic reaction to theophylline | 2 | [
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NCT02981173 | 1:33:treatment | lysergic acid diethylamide (LSD), or related compounds | 2 | [
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NCT01983462 | 24:33:treatment,,185:197:treatment,232:246:treatment,251:270:treatment | If currently receiving treatment with or taking any of the following supplements, be willing and able to discontinue taking them for 2 weeks prior and throughout the treatment period: Vitamin C, E or other multivitamins containing vitamin C or E; or omega-3 fatty acids | 2 | [
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NCT02593526 | 6:28:treatment | Post kidney transplantation | 2 | [
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NCT02310464 | 56:63:cancer,65:69:cancer,71:81:cancer,85:98:cancer | Histologically or cytologically confirmed diagnosis of gastric, lung, colorectal or breast cancer on file | 2 | [
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NCT02391402 | 20:37:chronic_disease | Clients who report suicidal ideation without imminent risk will be admitted into the study | 2 | [
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NCT01919619 | ,62:74:treatment | lactating females must agree not to breast-feed while taking lenalidomide | 2 | [
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NCT02747888 | 15:29:cancer | Families with thyroid cancer and a known genetic syndrome | 2 | [
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NCT02329652 | 8:19:chronic_disease | severe bradycardia | 2 | [
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NCT02131597 | 13:16:cancer,,,, | higher risk MDS (International Prognostic Scoring System [IPSS] int-2 or high; or >= 10% blasts as defined by World Health Organization [WHO]) | 2 | [
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NCT02848417 | 1:19:treatment | Immunosuppressives | 2 | [
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NCT02940288 | 46:53:treatment,,85:97:treatment,123:135:treatment | Patients will be withdrawn from the study if surgery time exceeds 90 minutes or the laparoscopic procedure turned into an open surgery | 2 | [
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NCT01773395 | 34:97:allergy_name | History of allergic reactions to compounds of similar chemical or biologic composition to GM-CSF | 2 | [
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NCT02355002 | 1:28:treatment | ventriculo-peritoneal shunt | 2 | [
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NCT03092011 | 70:73:chronic_disease | Babies being started on medication to control withdrawal symptoms of NAS | 2 | [
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NCT02203552 | 7:25:chronic_disease | Known bleeding disorders | 2 | [
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NCT02266329 | 8:29:treatment,39:50:treatment,54:71:treatment,83:94:treatment, | Use of prescribed stimulants (such as amphetamine or dextroamphetamine containing medications) within 2 weeks of beginning the preliminary screening period through the end of study involvement | 2 | [
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NCT02562430 | 44:53:treatment,72:80:chronic_disease,95:140:chronic_disease, | Subjects with medical contraindications to bupropion (e.g., history of seizures, uncontrolled electrolyte imbalance due to eating disorders, etc.) unless stable for 8 weeks prior to screening and there will be no changes during participation in the study | 2 | [
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NCT02803359 | 1:33:chronic_disease | Laryngopharyngeal Reflux Disease | 2 | [
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NCT02133898 | 1:32:treatment | Electroconvulsive Therapy (ECT) failure in past | 2 | [
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NCT02157610 | 22:36:treatment | Contraindication for nicotine patch use | 2 | [
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NCT02755116 | 30:48:treatment | Patient scheduled to undergo ambulatory surgery under general anesthesia | 2 | [
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NCT02003222 | 15:57:chronic_disease,,,,139:196:treatment,255:263:cancer | No history of acquired immune deficiency syndrome (AIDS)-related complications other than a history of low CD4+ T-cell count (< 200/mm^3) prior to initiation of combination antiretroviral therapy; on study CD4+ T-cell count may not be informative due to leukemia and should not be used as an exclusion criterion if low | 2 | [
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NCT02793921 | 20:26:cancer | Prior diagnoses of cancer | 2 | [
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NCT02955394 | 31:65:cancer | Current or previously treated brain or leptomeningeal metastases | 2 | [
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NCT01953900 | ,,65:83:treatment | killing of GD2-positive targets greater than or equal to 20% in cytotoxicity assay | 2 | [
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NCT02339233 | 1:12:chronic_disease | hypovolemia | 2 | [
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NCT02881242 | ,50:56:cancer | Hospitalization within 30 days of enrollment for cancer related events | 2 | [
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NCT01436968 | 1:16:treatment,21:36:cancer,45:49:treatment,53:56:treatment | Prior treatment for prostate cancer, except TURP or ADT | 2 | [
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NCT00715611 | 18:34:chronic_disease,48:68:treatment,70:79:treatment,84:105:treatment | Patients with an active infection that require systemic antibiotics, antiviral, or antifungal treatments | 2 | [
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NCT02169830 | 21:51:treatment, | Patient has used an investigational drug or device in the the 3 months prior to screening | 2 | [
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NCT02070549 | 37:65:chronic_disease | History or current evidence/risk of retinal vein occlusion (RVO) | 2 | [
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NCT02074631 | 22:37:cancer | History of a primary bone malignancy involving the lumbar spine | 2 | [
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NCT02131597 | 1:16:chronic_disease,18:27:chronic_disease,29:34:chronic_disease,45:54:chronic_disease,186:197:treatment,207:216:treatment | systemic fungal, bacterial, viral, or other infection not controlled (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment) | 2 | [
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NCT01851369 | 47:69:treatment | Patients who are actively receiving any other investigational agents | 2 | [
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NCT02451488 | ,,,122:149:treatment | who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and 2 weeks after cessation of the study drug | 2 | [
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NCT02994940 | 21:36:chronic_disease | Patients with known G6PD deficiency | 2 | [
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NCT02268448 | 16:40:treatment,52:59:treatment,61:76:treatment,81:101:treatment | Current use of chronic pain medications (including opioids, antidepressants and anti-epileptic drugs) | 2 | [
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