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NCT01908777 | 1:28:chronic_disease | Congenital long QT syndrome | 2 | [
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NCT02595372 | 1:22:treatment | Esomeprazole (Nexium) | 2 | [
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NCT02923921 | ,80:110:chronic_disease,112:135:chronic_disease | Clinically significant bleeding within two weeks prior to randomization (e.g., gastrointestinal (GI) bleeding, intracranial hemorrhage) | 2 | [
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NCT02146924 | 45:52:chronic_disease,74:90:chronic_disease,104:128:chronic_disease,130:154:chronic_disease,156:174:chronic_disease,194:211:chronic_disease,215:234:chronic_disease,235:252:chronic_disease | Research participants with any uncontrolled illness including ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, poorly controlled pulmonary disease or psychiatric illness/social situations that would limit compliance with study requirements | 2 | [
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NCT01140087 | 1:18:cancer | Active malignancy | 2 | [
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NCT02192359 | 48:100:treatment | Prospective participant is unable to undergo a magnetic resonance imaging (MRI) with contrast agent | 2 | [
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NCT02960113 | 22:55:treatment | Subjects who receive spinal and/or epidural anesthesia | 2 | [
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NCT02089607 | 1:33:chronic_disease,, | Thoracoabdominal aortic aneurysm with a diameter ≥ 5.5 cm or 2 times the normal aortic diameter | 2 | [
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NCT00914823 | 1:12:treatment | medications used to treat the subject's reproductive condition | 2 | [
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NCT02553460 | 15:25:cancer | Patients with T-cell ALL | 2 | [
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NCT02266784 | 32:48:chronic_disease | Has a primary diagnosis of any Axis II Disorder | 2 | [
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NCT02555189 | 29:44:treatment,48:57:treatment,,144:154:treatment | Patients on stable doses of bisphosphonates or denosumab which have been started no less than 4 weeks prior to enrollment may continue on this medication | 2 | [
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NCT02427581 | 39:61:cancer | Histologically confirmed diagnosis of invasive breast cancer | 2 | [
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NCT02920788 | 55:81:chronic_disease,93:103:chronic_disease,108:112:chronic_disease | Eligible participants may have other co-morbid stable neuropsychiatric disorders, including depression and PTSD | 2 | [
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NCT03084640 | 48:62:chronic_disease | Any concurrent uncontrolled illness, including mental illness or substance abuse, which in the opinion of the Investigator | 2 | [
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NCT02519322 | 80:83:treatment | following confirmation of their post-menopausal status, they can resume use of HRT during the study without use of a contraceptive method | 2 | [
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NCT02500381 | 16:36:treatment, | Stable dose of oral corticosteroids for at least 24 weeks | 2 | [
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NCT01974609 | 27:47:chronic_disease | those with a diagnosis of cognitive impairment | 2 | [
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NCT01639508 | 1:23:chronic_disease | malabsorption syndrome | 2 | [
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NCT03093909 | 77:93:chronic_disease,95:106:chronic_disease,119:134:chronic_disease,136:155:chronic_disease,157:193:chronic_disease,195:219:chronic_disease,221:239:chronic_disease,244:281:chronic_disease | Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, bradycardia, related to cardiac disease, bundle branch block, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study ... | 2 | [
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NCT02589977 | 1:15:chronic_disease | symptomatic HF | 2 | [
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NCT02169089 | 1:41:chronic_disease | Class III or IV Congestive Heart Failure | 2 | [
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NCT03058679 | ,25:40:treatment,,,88:98:treatment,102:112:treatment | Start or change dose of corticosteroids within 1 week of screening or a dose >20mg/day prednisone or equivalent | 2 | [
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NCT03027388 | 74:84:treatment | Patients must be in adequate general medical health to safely tolerate a craniotomy | 2 | [
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NCT02950337 | 1:18:chronic_disease | Diabetes mellitus with end organ damage | 2 | [
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NCT02004275 | 20:36:cancer | Primary refractory multiple myeloma, where primary refractory multiple myeloma is defined as disease that is nonresponsive | 2 | [
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NCT02397889 | 25:43:chronic_disease,54:67:chronic_disease,71:95:chronic_disease | diagnosis of a lifetime psychotic disorder including schizophrenia or schizoaffective disorder | 2 | [
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NCT01626079 | ,54:67:chronic_disease,,,,,,,,,, | The subject has had at least one hospitalization for heart failure in the 12 months prior to subject registration and/or a corrected brain natriuretic peptide (BNP) ≥300 pg/ml or corrected n-Terminal pro- brain natriuretic peptide NT-proBNP ≥1500 pg/ml measured within 90 days prior to subject registration (corrected re... | 2 | [
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NCT02343549 | 18:30:treatment | Have undergone a brain biopsy via stereotactic or open technique | 2 | [
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NCT02407171 | 10:58:treatment,16:25:treatment,65:72:treatment, | have had prior treatments with Tyrosine Kinase Inhibitors (e.g. Tarceva) require only a 72-hour washout period prior to starting protocol treatment | 2 | [
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NCT00903266 | 31:37:chronic_disease | active participation in other stroke recovery trials testing experimental interventions | 2 | [
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NCT02311361 | 1:11:treatment,13:20:treatment,26:42:treatment | Intranasal, inhaled, and topical steroids | 2 | [
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NCT00703105 | 33:44:treatment,,88:93:cancer,193:215:treatment | Patients must not have received irradiation for the four weeks prior to removal of the tumor and no previously irradiated tumor deposits may be used for tumor lysate in the development of the dendritic cell vaccine | 2 | [
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NCT02366871 | 121:129:treatment | WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drug(s) apixaban plus 5 half-lives of study drug apixaban (2.5 days) plus 30 days (duration of ovulatory cycle) for a total of 32.5 days post-treatment completion | 2 | [
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NCT02339233 | 1:15:chronic_disease,17:28:chronic_disease,30:37:chronic_disease,41:54:chronic_disease | cardiovascular, respiratory, bladder or renal disease unrelated to SCI | 2 | [
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NCT02826681 | 26:36:treatment,39:42:treatment,46:52:treatment,59:73:treatment | Previously randomized to Injectafer® (FCM or VIT-45) in a clinical trial | 2 | [
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NCT02371720 | 47:58:treatment, | Patients receiving automatic home delivery of medications since medication possession ratio is reflective of the patient initiation the refill when they have exhausted the home supply of HU | 2 | [
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NCT01789333 | 15:24:chronic_disease | Patients with nystagmus or any other condition that is severe enough to prevent steady gaze during the treatment | 2 | [
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NCT02488967 | 12:27:chronic_disease | History of cardiac disease | 2 | [
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NCT01928576 | 1:29:treatment,31:41:treatment,43:53:treatment,55:65:treatment,67:97:treatment,195:224:treatment,228:250:treatment | Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, anti-CTLA-4 antibody therapies, any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways, DNA methyltransferase therapy or HDAC inhibitor therapy | 2 | [
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NCT01474889 | 8:14:treatment,, | Use of RT-CGM (continuous glucose monitor) within last 4 weeks | 2 | [
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NCT02263729 | 6:23:chronic_disease,25:39:chronic_disease,41:46:chronic_disease,50:57:chronic_disease | Have diabetes mellitus, cardiovascular, renal or hepatic co-morbidities | 2 | [
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NCT03179397 | 10:28:treatment | Previous refractive surgery | 2 | [
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NCT02394535 | 17:27:treatment | patients taking cimetidine must have this drug discontinued | 2 | [
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NCT02530463 | 31:38:treatment,54:64:treatment,,91:121:treatment | Patients who are on high dose steroid (equivalent of prednisone more than 10 mg a day) or immune suppression medications | 2 | [
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NCT02061293 | 1:8:treatment,10:25:treatment,27:33:treatment,38:46:treatment, | Cocaine, psychostimulant, opioid, or cannabis dependence (past 12 months) | 2 | [
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NCT02496663 | 38:60:treatment | Patients who are receiving any other investigational agents | 2 | [
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NCT03029806 | 1:13:treatment, | Decongestant use in the past 2 weeks | 2 | [
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NCT03153319 | 1:26:chronic_disease,34:46:chronic_disease,48:63:chronic_disease | Hematologic abnormalities (e.g., pancytopenia, aplastic anemia) | 2 | [
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NCT02657993 | 6:12:cancer | Past cancer | 2 | [
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NCT02286687 | 12:42:chronic_disease,44:65:chronic_disease,69:84:chronic_disease,,130:137:treatment | History of cerebrovascular accident (CVA), myocardial infarction or unstable angina within the previous 6 months before starting therapy | 2 | [
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NCT02356861 | 48:54:cancer | Presence of a life-threatening disease such as cancer | 2 | [
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NCT02481310 | 27:56:chronic_disease,60:72:treatment,135:143:treatment | Patients who have a known gastrointestinal (GI) disease or GI procedure that could interfere with the oral absorption or tolerance of ixazomib including difficulty swallowing | 2 | [
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NCT02496663 | 129:153:chronic_disease,155:179:chronic_disease,181:206:chronic_disease | Any clinically important abnormalities in rhythm, conduction or morphology of resting electrocardiography (ECG) (e.g., complete left bundle branch block, third degree heart block, second degree heart block) | 2 | [
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NCT02401347 | 30:41:treatment,45:54:treatment,,137:155:treatment | If prior platinum agent (eg, carboplatin or cisplatin) has been administered, no evidence of progression, or within 8 weeks of stopping platinum treatment | 2 | [
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NCT01407809 | 1:18:chronic_disease | Visual field loss | 2 | [
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NCT02578732 | 15:31:chronic_disease,54:65:treatment,194:197:chronic_disease,199:210:chronic_disease,215:226:chronic_disease | Patients with active infection or fever (patients on antibiotics for infection or patients getting over a cold or seasonal virus are not excluded), or known historical or active infection with HIV, hepatitis B, or hepatitis C | 2 | [
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NCT01849146 | 1:35:chronic_disease,57:91:treatment,136:164:treatment | Human immunodeficiency virus (HIV)-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with AZD1775 (MK-1775) | 2 | [
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NCT01644591 | 89:111:cancer | Patients are excluded if there is radiographic or cerebrospinal fluid (CSF) evidence of leptomeningeal disease | 2 | [
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NCT02584647 | 77:103:treatment | these patients are at increased risk of lethal infections when treated with marrow suppressive therapy | 2 | [
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NCT02367196 | 16:22:cancer,, | Prior systemic cancer-directed treatments or investigational modalities ≤ 5 half lives or 4 weeks prior to starting CC-90002, whichever is shorter | 2 | [
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NCT02338232 | 1:29:treatment | Regimens for transplantation | 2 | [
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NCT02366871 | 20:54:treatment,56:62:treatment,64:68:treatment | Concomitant use of dual strong inhibitors or inducers (CYP3A4, P-gp) | 2 | [
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NCT02053363 | 8:30:chronic_disease | Active intravascular clotting | 2 | [
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NCT02911792 | 12:18:cancer | History of cancer | 2 | [
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NCT02188121 | 18:42:treatment,72:78:treatment,82:85:treatment, | Receiving active cardiovascular treatment, defined as receiving both a statin or ARB in the past three months | 2 | [
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NCT02913430 | 1:17:cancer, | Brain metastasis is allowed if previously treated, stable and off steroids for a minimum of 56 days | 2 | [
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NCT03075826 | 14:26:treatment,62:73:treatment,91:103:treatment,, | have had any chemotherapy (investigational or FDA approved) (hydroxyurea is permitted) or radiotherapy within 2 weeks prior to study entry or those who have not recovered from adverse events due to agents administered more than 2 weeks earlier | 2 | [
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NCT02332668 | ,,,42:47:cancer | between 3 years and <18 years of age for rrcHL participants | 2 | [
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NCT01715220 | ,,,,,135:144:treatment,150:174:treatment,178:185:treatment | Patients with right upper quadrant abdominal pain of less than 24 hours' duration between ages 18 and 60 years of age will be offered treatment with sublingual nitroglycerin or placebo | 2 | [
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NCT02487082 | 158:169:treatment | Drugs that induce or inhibit cytochrome P450 2D6 and cytochrome P450 3A4 (enzymes important for drug metabolism) will be allowed because any effects of such medications are likely to be lost in individual variability due to genetic polymorphisms | 2 | [
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NCT02816736 | 9:33:chronic_disease | Complex congenital heart disease | 2 | [
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NCT02133196 | 77:99:treatment | Patients who have decreased immune competence may be less responsive to the experimental treatment and more susceptible to its toxicities | 2 | [
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NCT01760655 | ,16:41:chronic_disease | Greater than 3 cytogenetic abnormalities or any one of the following cytogenetic abnormalities | 2 | [
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NCT01959698 | 1:36:chronic_disease,47:80:chronic_disease,91:127:chronic_disease | Hepatitis B surface antigen (HBsAg) negative, hepatitis B core antibody (HBcAb) negative, hepatitis B surface antibody (HBsAb) positive patients | 2 | [
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NCT02320292 | 18:23:chronic_disease,34:42:treatment,60:68:treatment | Subjects who are HBsAg negative, anti-HBs positive, and/or anti-HBc positive, but viral DNA negative are eligible | 2 | [
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NCT02527265 | 17:43:treatment, | Exposure to any investigational product(s) in the past 3 months or 5 half-lives, whichever is more | 2 | [
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NCT02233868 | 40:49:allergy_name | Have a history of allergic reaction to lidocaine (self-report, medical history) | 2 | [
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NCT01696734 | 24:35:chronic_disease | clinically significant bradycardia | 2 | [
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NCT01742299 | 48:66:treatment | Patient has been permanently discontinued from imatinib treatment in the parent study due to unacceptable toxicity, non-compliance to study procedures, withdrawal of consent or any other reason | 2 | [
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NCT01659203 | 23:73:cancer | Histologically proven primary soft tissue sarcoma of the retroperitoneum | 2 | [
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NCT02565966 | ,,,17:33:treatment | diet 3 -4 weeks prior to surgery | 2 | [
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NCT02269293 | 46:58:treatment | Patients must be willing and able to swallow oral tablets | 2 | [
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NCT01850758 | 1:19:chronic_disease | Bleeding disorders | 2 | [
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NCT02912572 | 16:24:treatment | The effects of avelumab on the developing human fetus are unknown | 2 | [
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NCT02913430 | ,,31:46:cancer | ALP ≤ 5X ULN in patients with bone metastases | 2 | [
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NCT02524275 | 31:64:treatment | Simultaneous participation in other therapeutic clinical trials will not be allowed | 2 | [
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NCT02343042 | 13:15:cancer | Symptomatic MM, based on IMWG guidelines | 2 | [
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NCT02768727 | 12:28:chronic_disease | History of seizure disorder | 2 | [
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NCT01584076 | 1:10:treatment, | Treatment with topical atropine within the past 4 weeks | 2 | [
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NCT02500602 | 52:56:chronic_disease | Meet DSM-5 criteria for current (i.e., last month) PTSD | 2 | [
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