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NCT02266823 | 110:128:chronic_disease, | unable to participate meaningfully in an intervention that involves group sessions (e.g., due to uncorrected hearing impairment, non-English-speaking) | 3 | [
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NCT02875301 | 13:27:treatment,29:38:treatment,40:46:treatment | Presence of metal implants (pacemaker, stents) that would be MR ineligible | 3 | [
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NCT01959698 | 64:78:treatment,82:103:treatment,105:139:treatment,, | Patients must have normal baseline cardiac function based upon echocardiogram or gated blood pool scan (multigated acquisition scan [MUGA]) with an ejection fraction >= 50% | 3 | [
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NCT02538198 | 31:65:chronic_disease,61:64:chronic_disease,95:120:treatment,129:133:chronic_disease | Patients seropositive for the human immunodeficiency virus (HIV), and/or those who are taking anti-retroviral treatment for HIV/AIDS | 3 | [
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NCT03016130 | 8:24:treatment, | Use of neutropenic diet within 72 hours prior to consent | 3 | [
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NCT03175978 | 1:30:chronic_disease, | Grade 3 peripheral neuropathy within 14 days before enrollment | 3 | [
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NCT02993900 | 31:43:cancer | Children do not develop these malignancies and therefore are not considered candidates for this trial | 3 | [
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NCT01861106 | ,,174:181:chronic_disease | Mutation in the GATA2 gene, or evidence of loss of expression of one allele of GATA2, by cDNA analysis performed by a CLIA certified laboratory, or the clinical syndrome of MonoMAC | 3 | [
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NCT01430390 | 25:35:treatment | Donor's high resolution HLA typing must be available for review | 3 | [
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NCT00357565 | 1:17:chronic_disease,29:44:treatment,56:72:treatment, | Active infection at time of transplantation (including active infection with Aspergillus or other mold within 30 days) | 3 | [
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NCT02903446 | 14:29:chronic_disease | Uncontrolled hyperthyroidism | 3 | [
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NCT02203903 | 23:26:treatment,28:35:treatment,46:92:treatment, | Patients who received ATG, Campath, or other T cell immunosuppressive monoclonal antibodies in the last 28 days | 3 | [
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NCT02525029 | 11:16:chronic_disease,12:16:chronic_disease,,,,64:67:treatment,, | High-Risk aGVHD (ARM 1): Pediatric or adult (ages 12-76 years) HCT recipients with high-risk acute GVHD, as determined by the refined MN acute GVHD risk score: http://z.umn.edu/MNAcuteGVHDRiskScore OR high risk on the basis of blood biomarkers (Ann Arbor Score 3 or amphiregulin ≥ 33 pg/ml) | 3 | [
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NCT02526212 | 12:18:treatment,, | Persistent opioid abuse (positive toxicology for an unprescribed opioid at most recent test or in 50% or more of collected tests in the previous 6 months.) | 3 | [
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NCT02338999 | 25:37:allergy_name | Known latex allergy for EndoPAT test | 3 | [
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NCT02990455 | 34:54:chronic_disease, | Meets DSM-5 criteria for current alcohol use disorder with the presence of 6 or more symptoms (i.e., current severity of severe) | 3 | [
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NCT03029702 | 12:21:allergy_name,23:32:allergy_name,36:41:allergy_name | Allergy to glyburide, metformin or sulfa | 3 | [
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NCT02304458 | 47:60:chronic_disease | Part D1: Patients with relapsed or refractory neuroblastoma | 3 | [
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NCT01807897 | 15:45:treatment | Presence of a left ventricular assist device | 3 | [
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NCT01919619 | 1:43:chronic_disease | Active life-threatening autoimmune disease | 3 | [
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NCT02911831 | 17:35:treatment,41:48:treatment,58:70:treatment | Willing to have IV tranexamic acid or a placebo prior to hysterectomy | 3 | [
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NCT02674984 | 12:23:allergy_name | allergy to antibiotics | 3 | [
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NCT03068442 | 11:33:treatment | plans for carotid endarterectomy | 3 | [
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NCT02945293 | 27:33:treatment,37:48:treatment,66:81:treatment,83:103:treatment,106:129:treatment,131:152:treatment | current regular use of an opioid or medications that involve the opioid receptor (naltrexone (vivitrol), buprenorphine (subutex), methadone (dolophine) | 3 | [
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NCT02912572 | 48:65:treatment | Patients must NOT have received any prior PARP inhibitor therapy | 3 | [
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NCT00630253 | ,,31:64:chronic_disease | In patients <18 years of age, moderately severe aplastic anemia is defined as having at least one | 3 | [
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NCT01522768 | 44:72:chronic_disease,81:106:chronic_disease,108:132:chronic_disease,,159:174:chronic_disease,196:206:chronic_disease,208:229:chronic_disease, | History or presence of clinically relevant cardiovascular abnormalities such as uncontrolled hypertension, congestive heart failure NYHA classification of 3, unstable angina or poorly controlled arrhythmia. Myocardial infarction within 6 months prior to study entry | 3 | [
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NCT02396199 | 1:18:chronic_disease,, | Saccular aneurysm with aortic diameter greater than 1.5 times the normal aortic diameter that is deemed to be at risk for rupture based upon physician interpretation | 3 | [
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NCT01815359 | 40:68:treatment | Subjects who have previously undergone intraperitoneal chemotherapy | 3 | [
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NCT02527265 | 10:18:chronic_disease,,68:80:chronic_disease,117:124:cancer,126:130:chronic_disease,135:156:chronic_disease,232:244:chronic_disease,263:276:chronic_disease, | Unstable diabetes control, defined as 2 or more episodes of severe hypoglycemia (i.e., an episode associated with a seizure, coma, or loss of consciousness) or any hospitalization or emergency room visit for poor diabetes control, ketoacidosis, hypoglycemia, or hyperglycemia within the preceding 3 months from screening | 3 | [
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NCT02353819 | 1:29:cancer | non-melanomatous skin cancer | 3 | [
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NCT02471430 | 8:30:treatment,68:85:treatment | Use of HIV protease inhibitor or other strong or moderately strong CYP3A4 inhibitors | 3 | [
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NCT02872857 | 19:37:chronic_disease,,, | History of severe hepatic impairment (Child-Pugh score of 10-15) | 3 | [
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NCT02411656 | 46:61:treatment,68:87:treatment,89:101:treatment,103:134:treatment,136:153:treatment,158:165:treatment,208:216:chronic_disease | Has not recovered from adverse events due to prior therapies, i.e. monoclonal antibody, chemotherapy, targeted small molecule therapy, radiation therapy, or surgery; (Note: subjects with grade 2 neuropathy, alopecia and general disorders and administration site conditions [per Common Terminology Criteria for Adverse Ev... | 3 | [
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NCT02004028 | 11:31:treatment,, | Use of an investigational drug within 28 days or 5 half-lives prior to first dose | 3 | [
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NCT02624258 | 28:57:cancer | Patients with known active CNS involvement by malignancy | 3 | [
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NCT02700178 | 12:39:allergy_name | Allergy to medical grade adhesive tape (used to secure sensors to skin) | 3 | [
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NCT02191488 | 23:44:chronic_disease | No serious associated psychiatric illnesses | 3 | [
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NCT00085982 | ,43:66:chronic_disease | Presence of at least one of the following metabolic abnormalities | 3 | [
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NCT02553161 | 22:28:chronic_disease | a DSM-5 diagnosis of autism | 3 | [
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NCT02163317 | 1:16:chronic_disease,24:48:chronic_disease,59:74:treatment, | Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months | 3 | [
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NCT02106052 | 11:29:treatment, | Undergone neuropsychological testing within the past 6-months | 3 | [
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NCT02739620 | 1:11:chronic_disease,13:21:chronic_disease,25:46:chronic_disease | autoimmune, vascular or neuromuscular disease that could alter skeletal muscle | 3 | [
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NCT02515773 | 23:40:chronic_disease,81:96:chronic_disease,111:130:treatment,185:202:chronic_disease,204:211:treatment,214:235:chronic_disease,237:245:treatment | Major neurological or medical illnesses that affect weight gain (e.g., unstable thyroid disease) or require a systemic medication that might impact weight or glucose regulation (e.g., diabetes mellitus [insulin], chronic renal failure [steroids]) | 3 | [
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NCT03096886 | 35:60:allergy_name,62:71:allergy_name,80:94:chronic_disease | Have MRI contraindications (e.g., foreign metallic implants, pacemaker, severe claustrophobia) | 3 | [
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NCT03154580 | ,23:39:chronic_disease | Recent (past 5 years) suicide attempts | 3 | [
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NCT01842399 | ,42:64:treatment | Females must be menopausal or have had a bilateral oophorectomy | 3 | [
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NCT02426476 | 1:21:chronic_disease,34:57:chronic_disease,64:86:chronic_disease,90:111:chronic_disease,119:136:chronic_disease | cognitive impairment (dementia), neurocognitive deficits, or a central nervous system or neurological disorder (e.g., Gulf War Syndrome) | 3 | [
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NCT02500602 | 37:44:chronic_disease | Individuals considered an immediate suicide risk or who are likely to require hospitalization during the course of the study | 3 | [
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NCT02531711 | 14:39:chronic_disease,56:70:chronic_disease,72:87:chronic_disease,92:114:chronic_disease | MRI-verified lumbosacral radiculopathy associated with herniated disc, spinal stenosis, or post-surgical fibrosis | 3 | [
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NCT03158974 | 30:51:chronic_disease,, | Have a clinical diagnosis of condylomata acuminata with ≥2 but ≤10 visible external genital warts (EGWs) | 3 | [
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NCT02355535 | 49:54:chronic_disease | Presence of any non-healing wound, fracture, or ulcer | 3 | [
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NCT03151330 | ,79:90:chronic_disease,92:109:chronic_disease,111:125:chronic_disease,127:140:chronic_disease,142:153:chronic_disease,155:186:chronic_disease,188:204:chronic_disease | Major structural anomalies that may shorten pregnancy- examples would include anencephaly, holoprosencephaly, schizencephaly, gastroschisis, omphalocele, congenital diaphragmatic hernia, pyloric stenosis, etc | 3 | [
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NCT02876510 | 8:24:chronic_disease | active Hepatitis B or C infection | 3 | [
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NCT02299414 | ,12:32:chronic_disease,,,,,,,175:186:treatment,202:218:treatment,, | Women with chronic hypertension in pregnancy with new or untreated chronic hypertension, blood pressure 140-159 systolic or 90-104 diastolic OR known chronic hypertension on monotherapy and taking any antihypertensive and blood pressure ≤159/104 (including those with blood pressure <140/90) | 3 | [
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NCT02544880 | 1:16:treatment | Salvage surgery is not recommended as per National Comprehensive Cancer Network (NCCN) guidelines, or after multidisciplinary treatment evaluation, including those with surgically unresectable disease at primary site or regional lymph nodes | 3 | [
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NCT02531295 | 19:31:chronic_disease,53:56:treatment,61:111:treatment | Positive test for tuberculosis by either skin test (PPD) or blood interferon-gamma release assay (QuantiFERON) | 3 | [
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NCT01333046 | 6:14:cancer,20:37:cancer,72:75:cancer,90:108:treatment | with lymphoma as a second malignancy e.g. a Richters transformation of CLL after failing front line therapy | 3 | [
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NCT02578732 | 159:167:treatment | Patients with serious medical risk factors involving any of the major organ systems such that the investigator considers it unsafe for the patient to receive FOLFOX-A | 3 | [
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NCT02321501 | 42:52:allergy_name,62:71:allergy_name,86:95:allergy_name,97:109:allergy_name | Known intolerance or hypersensitivity to everolimus or other rapamycin analogs (e.g. sirolimus, temsirolimus) | 3 | [
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NCT02578641 | 73:76:cancer | Subjects will be enrolled based on confirmed histology diagnosis of the NPC | 3 | [
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NCT02464878 | 10:30:treatment, | with the graft pancreatectomy occurring more than 6 months ago | 3 | [
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NCT01795313 | 76:97:treatment,,215:236:cancer,250:278:cancer,309:331:treatment | must have previously received standard initial therapy including attempted gross total resection, where safely feasible, and in appropriate circumstances (e.g., those older than one year at initial diagnosis, with non-metastatic tumors and at least microscopic residual disease), involved field fractionated radiation th... | 3 | [
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NCT02091141 | 1:19:cancer,21:45:cancer,47:64:cancer,69:91:cancer,111:118:cancer | Malignant melanoma, papillary thyroid cancer, colorectal cancer, or hematologic malignancy including multiple myeloma | 3 | [
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NCT02484404 | 19:52:treatment | Patients who were previously treated with cediranib are ineligible | 3 | [
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NCT02945800 | 35:49:cancer,97:109:treatment,102:109:treatment, | Potential participants with known CNS metastases are excluded unless treated surgically or with radiotherapy and stable with no recurrent lesions for at least 3 months from the start of protocol therapy | 3 | [
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NCT02431806 | 13:20:chronic_disease | Significant suicide risk | 3 | [
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NCT02013492 | 64:83:chronic_disease,197:212:treatment,216:219:treatment,245:248:cancer | For patients whose CURRENT disease is vascular only: Enhancing vascular thrombosis (involving portal vein, IVC and/or hepatic vein) demonstrating early arterial enhancement and delayed washout on multi-phasic CT or MRI, in a patient with known HCC (diagnosed according to criteria in (a) or (b) | 3 | [
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NCT01817751 | 24:36:chronic_disease,38:51:chronic_disease,56:79:chronic_disease | History of significant intratumoral, intracerebral, or subarachnoid hemorrhage | 3 | [
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NCT01608438 | 149:166:treatment,174:198:treatment,202:218:treatment,220:246:treatment,252:262:treatment | Any metal in head with the exception of dental work or any ferromagnetic metal elsewhere in the body. This applies to all metallic hardware such as cochlear implants, or an Internal Pulse Generator or medication pumps, implanted brain electrodes, and peacemaker | 3 | [
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NCT02503722 | 46:61:treatment | Patients with enteric stomata or significant bowel resection | 3 | [
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NCT02562066 | 1:17:chronic_disease | Seizure disorder | 3 | [
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NCT02560766 | 44:64:chronic_disease,96:106:chronic_disease,108:138:treatment,141:157:chronic_disease,162:175:chronic_disease | Current or past history of any significant psychiatric disorder including, but not limited to, depression (treatment with antidepressants), bipolar disorder, or schizophrenia | 3 | [
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NCT02122185 | 47:62:treatment,107:121:cancer,166:185:treatment,192:202:treatment,206:217:treatment | subjects should not be participating in other clinical trials of interventions designed to reduce risk of ovarian cancer recurrence or plan to receive off -protocol maintenance therapy (e.g. paclitaxel or bevacizumab) | 3 | [
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NCT02366871 | 17:43:chronic_disease | homozygotes for Factor V Leiden deficiency | 3 | [
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NCT02310399 | 8:19:treatment | Failed revision CI without benefit | 3 | [
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NCT02579265 | 1:14:chronic_disease | Gastroschisis | 3 | [
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