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NCT02234934 | 54:64:treatment | patients with a correctable deficiency controlled on medication | 1 | [
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NCT01684904 | 16:26:cancer,35:63:cancer,,118:145:cancer,147:158:cancer,163:169:cancer | Prior invasive malignancy (except non-melanomatous skin cancer), unless disease free for a minimum of 2 years ( e.g. carcinoma in situ of breast, oral cavity, or cervix are permissible) | 1 | [
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NCT03118050 | 1:13:chronic_disease | Pre-diabetes per American Diabetes Association criteria | 1 | [
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NCT01684397 | 1:16:chronic_disease | Unstable angina | 1 | [
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NCT03070535 | 1:26:chronic_disease | cholesterol abnormalities as defined by the Adult Treatment Panel III classification | 1 | [
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NCT02912572 | 1:19:cancer | Endometrial cancer is very rare in the pediatric population | 1 | [
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NCT02497300 | 1:30:chronic_disease | Diabetes mellitus (DM) type 1 | 1 | [
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NCT02875301 | 1:13:chronic_disease | brain injury | 1 | [
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NCT03115424 | 18:30:chronic_disease,32:46:chronic_disease,50:63:chronic_disease | Prior history of pancreatitis, cholelithiasis or cholecystitis | 1 | [
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NCT02340156 | 61:74:treatment | Radiographic demonstration of disease progression following prior therapy | 1 | [
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NCT01618357 | 1:8:treatment,19:34:treatment,59:63:treatment,98:101:treatment | Surgery: Incident breast biopsies only permitted prior to POPI to confirm residual disease after NAC | 1 | [
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NCT03167606 | 13:16:chronic_disease | Self-report HIV-negative or unknown status | 1 | [
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NCT02822378 | 1:16:treatment,,, | bisphosphonates, parathyroid hormone or strontium within the past 12 months | 1 | [
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NCT02476409 | 20:33:treatment | Daily oral dose of loop diuretic | 1 | [
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NCT02287558 | ,,,,,,205:217:treatment,,, | Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10 - 14 days prior to and again within 24 hours of prescribing pomalidomide and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable me... | 1 | [
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NCT02721303 | 10:23:chronic_disease | Advanced organ failure | 1 | [
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NCT02167009 | 12:19:allergy_name | History of gelatin allergy | 1 | [
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NCT02089607 | 37:52:allergy_name,54:61:allergy_name,56:59:allergy_name,63:72:allergy_name,74:80:allergy_name,87:93:allergy_name,96:109:allergy_name,111:115:allergy_name,117:125:allergy_name,129:133:allergy_name | Known sensitivities or allergies to stainless steel, nitinol, polyester, solder (tin, silver), polypropylene, PTFE, urethane or gold | 1 | [
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NCT02312570 | 1:21:chronic_disease,33:58:chronic_disease,61:71:chronic_disease,73:92:chronic_disease,94:97:chronic_disease,105:118:chronic_disease | Rheumatoid arthritis (and other collagen vascular disease), vasculitis, sickle cell disease, HIV Severe liver disease | 1 | [
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NCT01807611 | 1:4:chronic_disease | HIV negative | 1 | [
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NCT03145298 | 1:15:chronic_disease | LV dysfunction | 1 | [
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NCT02215096 | 7:23:chronic_disease,34:50:treatment,54:83:treatment | Known active infection requiring intravenous (IV) or oral anti-infective treatment | 1 | [
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NCT02234557 | 14:37:chronic_disease,39:70:chronic_disease,72:90:chronic_disease,95:101:chronic_disease | diagnosis of Intellectual Disability, Developmental Language Disorder, Reading Disability, or Autism (screened for using the Social Competence Questionnaire (SCQ) | 1 | [
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NCT02178566 | 10:21:chronic_disease,, | Systemic hypotension with systolic blood pressure < 85 mmHg | 1 | [
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NCT02349867 | ,,,145:154:treatment | Bronchopulmonary hemorrhage/bleeding event >= grade 2 (Common Terminology Criteria for Adverse Events [CTCAE] v4.0) within 12 weeks prior to of treatment | 1 | [
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NCT02498301 | 1:20:treatment | warfarin (Coumadin) | 1 | [
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NCT02634957 | 1:10:cancer | Dysplasia | 1 | [
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NCT02588664 | 1:47:chronic_disease | subdural or aneurysmal subarachnoid hemorrhage | 1 | [
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NCT01524536 | 23:37:treatment | subjects on a current corticosteroid taper | 1 | [
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NCT02187198 | 1:28:chronic_disease,39:48:chronic_disease,50:81:chronic_disease | serious psychiatric illness including psychosis, bipolar disorder with psychosis | 1 | [
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NCT02607514 | 1:20:chronic_disease | psychotic disorders | 1 | [
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NCT02527200 | 12:24:chronic_disease | History of pancreatitis (acute or chronic) | 1 | [
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NCT02950337 | 34:44:cancer, | Patients with a known history of malignancy with a disease-free interval <3 years prior to enrollment | 1 | [
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NCT02101736 | 77:92:chronic_disease | Dental braces or prosthesis that interferes with volumetric analysis of the neurofibroma(s) | 1 | [
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NCT02642939 | 13:29:chronic_disease | Significant cardiac diseases includes second/third degree heart block | 1 | [
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NCT02932280 | 25:57:chronic_disease,52:56:chronic_disease,71:96:treatment | Active acute or chronic graft-versus-host-disease (GvHD) or receiving immunosuppressive therapy as treatment for GvHD | 1 | [
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NCT02313428 | 18:37:treatment | Ulcer in area of radiation treatment | 1 | [
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NCT02493530 | 12:38:chronic_disease,40:55:chronic_disease,57:78:chronic_disease,83:105:chronic_disease, | History of cerebral vascular accident, unstable angina, myocardial infarction, or ventricular arrhythmia within the last 6 months | 1 | [
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NCT03188042 | 30:38:chronic_disease | Other optic comorbidity than glaucoma | 1 | [
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NCT02234934 | 53:63:treatment | Contraindication for administration of conditioning medication | 1 | [
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NCT03040778 | 22:36:treatment | Patients taking oral anticoagulants | 1 | [
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NCT02636283 | 26:51:chronic_disease | Subject with symptoms of intermittent claudication, such as exercise-induced pain, cramps, fatigue, or other equivalent discomfort, involving large muscle groups of the leg(s) (calf, thigh, buttocks), relieved by rest | 1 | [
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NCT03043963 | 1:9:chronic_disease,, | diabetic patients who are insulin dependent (or have HbA1c>9.0%) | 1 | [
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NCT02772562 | 1:42:treatment | Prior solid organ or stem cell transplant | 1 | [
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NCT01877382 | 5:34:treatment,38:51:treatment,,74:94:treatment | Had therapeutic radiation therapy or major surgery within 4 weeks before study drug treatment | 1 | [
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NCT03041844 | 81:89:chronic_disease | DUs must be present on the ankle or foot and be secondary to complications from diabetes | 1 | [
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NCT02796209 | 21:32:allergy_name | Hypersensitivity to atomoxetine (severe allergic reaction, rash, urticaria, anaphylaxis) | 1 | [
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NCT02291523 | 15:37:treatment, | Have received probiotic preparations ≤ 4 weeks prior to randomization | 1 | [
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NCT02574455 | ,35:59:treatment,, | At least 2 weeks beyond high dose systemic corticosteroids (however, low dose corticosteroids < 20 mg prednisone or equivalent daily are permitted) | 1 | [
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NCT02481245 | 1:20:chronic_disease | delusional disorder | 1 | [
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NCT03188185 | 50:62:chronic_disease,64:75:chronic_disease,80:89:chronic_disease | Has any other significant medical condition (eg, neurological, psychiatric, or metabolic) or clinical symptom that could unduly risk the subject or affect the interpretation of study data | 1 | [
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NCT00911560 | ,,178:190:treatment | stage 4 with (any age) or without (>18 months old) MYCN amplification, MYCN-amplified stage 3 (unresectable; any age), MYCN-amplified stage 4S, or disease resistant to standard chemotherapy | 1 | [
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NCT01522768 | 65:76:treatment,108:114:treatment,131:138:treatment | Patients who have previously provided samples at any time after trastuzumab resistance will be exempt from biopsy at the start of therapy | 1 | [
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NCT02358187 | 28:47:treatment | Patients who have received prior immunotherapy | 1 | [
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NCT03143985 | 41:72:treatment | Patients who are primarily eligible for autologous stem cell transplant | 1 | [
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NCT03006562 | 22:25:treatment | Active treatment for VTE | 1 | [
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NCT02516670 | 81:97:chronic_disease,111:135:chronic_disease,137:161:chronic_disease,163:181:chronic_disease,186:223:chronic_disease | Have uncontrolled intercurrent illness, including but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements | 1 | [
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NCT03113695 | ,109:118:treatment | Males must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy | 1 | [
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NCT01827384 | 89:98:treatment | patients on other trials will be eligible as long as they are no longer receiving study treatment | 1 | [
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NCT02589977 | 7:29:chronic_disease,31:51:chronic_disease,62:81:treatment | known cardiovascular disease, cardiac risk factors or use of cardiac medications | 1 | [
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NCT02547818 | 46:57:treatment,,114:145:treatment,153:162:treatment, | subjects must be on a stable dose of current medications for 4 weeks prior to study entry, with the exception of acetylcholinesterase inhibitors and/or memantine, which must be on a stable dose for at least 12 weeks prior to study entry | 1 | [
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NCT01919619 | ,,,,128:140:treatment, | diffusing capacity of the lung for carbon monoxide (DLCO) >= 40% within 3 months of study entry (or within 1 month if received chemotherapy within the past 3 months) | 1 | [
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NCT02464436 | 23:57:chronic_disease,59:76:chronic_disease,78:95:chronic_disease | Negative serology for human immunodeficiency virus (HIV), hepatitis B (HBV), hepatitis C (HCV) | 1 | [
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NCT01676753 | 24:58:chronic_disease | Patient is known to be Human Immunodeficiency Virus (HIV)-positive | 1 | [
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NCT02524275 | ,,,,194:203:treatment | Women of reproductive potential must be non-pregnant and non-nursing and must agree to employ an effective barrier method of birth control throughout the study and for up to 6 months following treatment | 1 | [
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NCT01597518 | 1:11:treatment | Mexiletine | 1 | [
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NCT00737893 | 31:44:treatment,54:87:treatment,94:131:treatment | Scheduled to undergo curative prostatectomy applying bilateral nerve-sparing procedure, with intact pre-surgical erectile function | 1 | [
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NCT02192398 | 16:33:treatment,16:25:treatment,77:86:treatment,90:103:treatment,110:118:treatment,120:127:treatment,170:191:treatment,209:213:chronic_disease | Currently in a treatment program for alcohol or drug abuse, or currently on methadone or buprenorphine (i.e. suboxone, subutex) for treatment of addiction, or currently prescribed stimulants for treatment of ADHD | 1 | [
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NCT01647321 | 19:60:chronic_disease | Subjects having a Stage 2 or greater sacral decubitus ulcer | 1 | [
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NCT03078530 | 1:4:chronic_disease,6:13:chronic_disease,15:24:chronic_disease,26:33:chronic_disease,37:54:chronic_disease | HIV, cardiac, pulmonary, hepatic or renal dysfunction | 1 | [
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NCT02323880 | 1:30:treatment,,72:101:treatment,,120:131:treatment | Myelosuppressive chemotherapy: At least 21 days after the last dose of myelosuppressive chemotherapy (42 days if prior nitrosourea) | 1 | [
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NCT01660607 | 31:42:chronic_disease | PCR+ or sAg (surface antigen) hepatitis B | 1 | [
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NCT02844738 | 1:11:treatment,17:36:treatment,,88:111:chronic_disease | Treatments with strong opioid drugs in the previous 4 weeks for other pain rather than shoulder osteoarthritis | 1 | [
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NCT02639065 | 12:49:chronic_disease | History of psychiatric illness/social situations that would limit compliance with study requirements or compromise the ability of the subject to give written informed consent | 1 | [
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NCT02541565 | ,,,,,233:243:treatment | Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication | 1 | [
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NCT01526603 | 43:55:treatment, | Patients who are delayed in consolidation chemotherapy beyond 8 weeks | 1 | [
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NCT02881320 | 42:61:treatment,63:78:treatment,83:128:treatment | No documented or suspected resistance to emtricitabine (FTC), tenofovir (TFV), or integrase strand transfer inhibitors (INSTIs) including, but not limited to, the reverse transcriptase resistance mutations K65R and M184V/I | 1 | [
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NCT02362997 | 64:80:chronic_disease,94:118:chronic_disease,120:135:chronic_disease,146:164:chronic_disease,169:188:chronic_disease | Uncontrolled illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements or pose excess risk to the participant in the opinion of the t... | 1 | [
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