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NCT03072238 | 1:20:chronic_disease | Progressive disease before initiating study treatment | 3 | [
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NCT02070549 | 12:36:chronic_disease,48:69:chronic_disease,74:89:chronic_disease,92:112:treatment,117:125:treatment, | History of acute coronary syndromes (including myocardial infarction and unstable angina), coronary angioplasty, or stenting within 6 months prior to randomization | 3 | [
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NCT02266823 | ,105:110:chronic_disease | unable to read or otherwise use an iPad to monitor dietary intake, physical activity, and weight (e.g., blind, illiterate) | 3 | [
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NCT00338377 | 34:55:treatment | Patients must be able to undergo contrast-enhanced MRI. (Cohort D) | 3 | [
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NCT02137122 | 1:4:treatment,,41:55:chronic_disease,57:71:treatment | MRI contraindications (e.g., pregnancy, claustrophobia, metal implants) | 3 | [
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NCT02937402 | 67:85:chronic_disease,109:117:chronic_disease,157:186:treatment | Subjects with an active or recent history of a known or suspected autoimmune disease or recent history of a syndrome that required systemic corticosteroids/immunosuppressive medications | 3 | [
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NCT02353819 | 10:29:treatment | Previous pelvic radiotherapy | 3 | [
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NCT01505569 | 27:42:allergy_name | Known contraindication to PBSC collection | 3 | [
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NCT02807272 | 25:34:chronic_disease,36:41:chronic_disease,46:63:chronic_disease,75:91:treatment | Active and uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy | 3 | [
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NCT01356290 | 1:17:chronic_disease | Active infection | 3 | [
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NCT01474889 | 1:8:treatment, | Insulin-dependent for > 10 years | 3 | [
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NCT03030118 | 44:77:treatment,101:115:chronic_disease,117:135:chronic_disease,137:146:chronic_disease,148:157:chronic_disease,177:190:allergy_name | The subject has other contraindications to treatment with hydroxychloroquine including pre-existing ocular disease, hepatic impairment, psoriasis, porphyria, or allergy to the drug or class | 3 | [
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NCT02172651 | ,,108:130:treatment,132:144:treatment,146:170:treatment,175:197:treatment,, | Women of child-bearing potential include any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or is not postmenopausal (defined as amenorrhea ≥12 consecutive months | 3 | [
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NCT02366819 | 12:33:cancer | revious or concurrent malignancy | 3 | [
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NCT00573027 | 9:31:chronic_disease,64:76:treatment,80:91:treatment | Primary valvular heart disease clearly indicating the need for valve repair or replacement | 3 | [
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NCT02091999 | ,16:26:treatment | ≥ 40 mg/day of prednisone | 3 | [
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NCT03153969 | 55:74:treatment | Evidence of severe bruxing or clenching or in need of TMJ related therapy | 3 | [
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NCT01964859 | 21:41:treatment, | Having received any investigational drug within 30 days prior to study entry | 3 | [
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NCT03040778 | 22:35:chronic_disease | Patients with severe liver disease | 3 | [
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NCT02532452 | 13:16:treatment,20:31:treatment,,50:62:treatment | Infusion of ATG or alemtuzumab within 2 weeks of CTL infusion | 3 | [
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NCT02383927 | 1:14:treatment, | Major surgery, other than diagnostic surgery, within 4 weeks prior to first dose, without complete recovery | 3 | [
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NCT02905370 | 1:20:chronic_disease | Atrial fibrillation | 3 | [
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NCT02589938 | 21:33:treatment, | Must have completed radiotherapy at least 12 months prior to entry | 3 | [
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NCT03100435 | 28:48:treatment, | Subjects with a history of antibiotic treatment within the last six months | 3 | [
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NCT01758042 | 26:29:chronic_disease,31:34:chronic_disease,39:44:chronic_disease | Serologic positivity for HIV, HCV, or HbsAg positivity | 3 | [
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NCT02043548 | 20:28:treatment | 1 week washout for anakinra | 3 | [
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NCT02428205 | 55:66:treatment,68:76:chronic_disease,78:111:chronic_disease,113:128:chronic_disease,130:146:chronic_disease,160:167:chronic_disease,169:190:chronic_disease,235:248:allergy_name,, | Any of the following exclusionary criteria related to propranolol (diabetes, reactive airway/pulmonary disease, thyroid disease, bradyarrhythmias, unexplained syncope, narrow angle glaucoma, known hypersensitivity/adverse reaction to beta-blockers, potentially interacting drugs, underweight < 15 kg) | 3 | [
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NCT02131597 | 9:33:cancer,35:52:cancer,57:91:cancer,176:185:treatment | treated non-melanoma skin cancer, in situ carcinoma, or cervical intraepithelial neoplasia, regardless of the disease-free duration, are eligible for this study if definitive treatment for the condition has been completed | 3 | [
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NCT03183128 | 28:46:treatment | The requirement of CDI SOC antibiotic therapy | 3 | [
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NCT01891812 | 1:25:chronic_disease | life-threatening illness as determined by attending clinician | 3 | [
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NCT01871766 | 15:27:treatment,,82:88:treatment,92:110:treatment | Initiation of chemotherapy is planned within 6 weeks (42 days) of the definitive biopsy or surgical resection | 3 | [
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NCT02331095 | 15:21:treatment, | Patients with statin use within 6 weeks of enrollment | 3 | [
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NCT02114229 | 31:36:cancer | Patients with newly diagnosed AT/RT | 3 | [
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NCT02013154 | ,,,45:60:chronic_disease,62:83:chronic_disease,,119:129:chronic_disease | New York Heart Association Class III or IV, cardiac disease, myocardial infarction within the past 6 months, unstable arrhythmia | 3 | [
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NCT02579044 | 15:37:chronic_disease,92:100:treatment,115:122:treatment,126:142:treatment | Subjects with endocrine deficiencies are allowed to receive physiologic or stress doses of steroids if necessary. Topical or inhaled steroids are allowed | 3 | [
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NCT03069469 | ,,,,,107:123:chronic_disease | QT interval corrected by Fridericia's formula (QTcF) >450 ms in males or >470 ms in females or history of long QT syndrome | 3 | [
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NCT02483728 | 17:30:treatment | Able to undergo patch testing | 3 | [
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NCT02442622 | 1:21:chronic_disease | rheumatoid arthritis | 3 | [
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NCT02256631 | 20:48:treatment, | Mother received no antiretroviral therapy (ART) during pregnancy | 3 | [
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NCT01975597 | 15:39:cancer | Patients with metastatic breast cancer | 3 | [
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NCT01712308 | 1:26:chronic_disease | Uncontrolled hypertension | 3 | [
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NCT02646787 | 13:35:chronic_disease | Evidence of traumatic brain injury | 3 | [
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NCT00492778 | 16:35:chronic_disease | no evidence of extrapelvic disease | 3 | [
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NCT02924363 | 1:27:chronic_disease | serious concurrent illness | 3 | [
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NCT02584647 | ,,,,,244:254:treatment | Women of child-bearing potential must have a negative serum pregnancy test at screening and must agree to use an effective form of contraception from the time of the negative pregnancy test and for a minimum of 3 months after the last dose of study drug | 3 | [
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NCT01906385 | 29:47:chronic_disease,51:74:chronic_disease,85:88:treatment,92:125:treatment | The subject has evidence of acute intracranial or intratumoral hemorrhage either by MRI or computerized tomography (CT) scan | 3 | [
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NCT02037048 | 1:22:treatment,24:41:treatment,46:53:treatment,63:73:cancer | No prior chemotherapy, radiation therapy, or surgery for this malignancy will be allowed | 3 | [
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NCT02555280 | 1:15:chronic_disease,, | Morbid obesity defined as a body mass index > 40 | 3 | [
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NCT02272049 | 16:30:chronic_disease | Participant is claustrophobic and unable to tolerate the imaging | 3 | [
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NCT03016351 | 1:15:chronic_disease,,,, | Hyperlipidemia, with an LDL-C >159 mg/dL and /or total-C >229 mg/dL | 3 | [
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NCT03100461 | 12:30:cancer | history of adenomatous polyps | 3 | [
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NCT02519322 | 24:36:chronic_disease,38:48:chronic_disease,66:74:chronic_disease | A confirmed history of encephalitis, meningitis, or uncontrolled seizures in the year prior to informed consent | 3 | [
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NCT03186872 | 11:27:treatment | Stable on psychiatric meds for 4 weeks | 3 | [
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NCT02473276 | 12:20:allergy_name | Allergy to morphine | 3 | [
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NCT03132636 | 11:27:cancer | Untreated brain metastasis that may be considered active | 3 | [
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NCT02412540 | 1:38:chronic_disease | alpha-1-antitrypsin (A1AT) deficiency | 3 | [
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NCT02285101 | 14:30:treatment,37:49:treatment,,158:169:treatment | Has received cancer treatment, e.g. chemotherapy, targeted biologic or enzymes, either approved or investigational, within 4 weeks prior to the start of the PEG-BCT-100 | 3 | [
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NCT01986205 | 25:30:chronic_disease,34:47:chronic_disease,108:118:treatment | Chronic disease such as heart or renal failure would raise the participant's risk of adverse events during hyperbaric oxygen | 3 | [
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NCT01917929 | 36:52:chronic_disease | Patient has an active or suspected latent infection in or about the affected hip joint at time of study device implantation | 3 | [
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NCT02466009 | 26:51:cancer | Histologically confirmed colorectal adenocarcinoma | 3 | [
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NCT02769611 | ,,67:76:chronic_disease | Patients with serum albumin less than 3 g/dL or evidence of liver cirrhosis | 3 | [
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NCT01313533 | 18:60:treatment,66:95:treatment,,120:124:treatment | Participation in another interventional investigative study of a cardiovascular drug or device within 30 days prior to CABG | 3 | [
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NCT01626079 | 16:49:treatment,16:55:treatment,98:132:treatment, | Implant of any Cardiac Resynchronization Therapy (CRT) or Cardiac Resynchronization Therapy with cardioverter-defibrillator (CRT-D) within the last 30days prior to subject registration | 3 | [
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NCT02519322 | 5:18:treatment, | Any major surgery within the last 3 weeks | 3 | [
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NCT03073070 | 18:31:chronic_disease,, | prior history of liver disease with transaminases more than 3 times the upper limit of normal for age | 3 | [
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NCT02379819 | 53:65:chronic_disease | Moderately severe to profound mid to high frequency hearing loss in the contralateral ear | 3 | [
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NCT02751151 | ,25:29:cancer | History of at least one NMSC | 3 | [
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NCT02095808 | 1:20:chronic_disease | Sickle cell disease | 3 | [
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NCT03042689 | 1:25:chronic_disease | Congestive heart failure | 3 | [
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NCT02847689 | 1:26:chronic_disease | Twin-to-twin transfusions | 3 | [
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NCT02416102 | 7:29:chronic_disease, | Acute pulmonary exacerbation within 6 weeks from the Screening Visit | 3 | [
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NCT03168776 | 14:50:treatment | for emergent coronary bypass graft (CABG) surgery | 3 | [
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NCT03137173 | 14:72:chronic_disease | Diagnosis of acute bacterial skin and skin structure infection (ABSSSI), with a regional or systemic sign of infection | 3 | [
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NCT03053518 | 34:51:treatment | have had or are planning to have bariatric surgery during the study | 3 | [
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NCT02255383 | 13:92:treatment | Patient has previously received partial or total knee arthroplasty for the ipsilateral knee | 3 | [
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NCT02574910 | 24:42:chronic_disease | Patients with baseline hepatic impairment are excluded from this trial | 3 | [
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NCT03079401 | 30:55:allergy_name | Patient has known allergy to mouse and/or cow products | 3 | [
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NCT02573883 | 20:34:treatment | excluding sling or sacrocolpopexy mesh | 3 | [
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NCT02888119 | 30:38:chronic_disease,40:48:chronic_disease,50:56:cancer,58:82:chronic_disease,87:114:chronic_disease | Major co-morbidities such as diabetes, mellitus, cancer, congestive heart failure and chronic infectious diseases | 3 | [
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NCT02013154 | 26:48:allergy_name | Significant allergy to a pharmaceutical therapy that, in the opinion of the investigator, poses an increased risk to the participant | 3 | [
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NCT02453373 | 41:56:allergy_name | Patients with known hypersensitivity to nickel-titanium | 3 | [
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NCT00924027 | 15:50:cancer,59:72:treatment,106:129:treatment,141:152:treatment | Patients with localized prostate cancer (T1b-T3b) in whom brachytherapy will be integrated as a boost to external beam radiation or used as monotherapy for definitive management | 3 | [
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NCT02085941 | 102:128:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to gadolinium contrast agents, if contrast use is anticipated during the procedure | 3 | [
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NCT01967238 | 11:24:chronic_disease,39:66:chronic_disease,83:105:chronic_disease | Confirmed HIV infection, positive for hepatitis B surface antigen or positive for hepatitis C antibodies | 3 | [
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NCT00285935 | 10:26:treatment | Negative urine toxicology (drugs of abuse) screen | 3 | [
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NCT01367444 | 31:34:chronic_disease, | with early or childhood-onset SMD with at least one pathogenic mutant ABCA4 allele on each chromosome confirmed by direct sequencing and co-segregation analysis within the patient's family | 3 | [
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NCT02371720 | 21:24:chronic_disease | Have a diagnosis of SCD, with either βS/βS, βS/βC, βS/βD , βS/β0 , βS/βO-Arab, or βS/β+ genotype | 3 | [
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NCT02668744 | 31:44:chronic_disease,63:85:chronic_disease,87:93:cancer | Previously diagnosed with any major illness since birth (e.g. chronic birth asphyxia, cancer, etc.) | 3 | [
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NCT03004807 | 11:23:treatment,24:42:treatment,46:60:treatment, | Consume a multivitamin/mineral supplement or placebo tablet each day during the 6-month study period | 3 | [
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NCT02400554 | ,30:37:treatment,45:51:treatment,53:69:treatment,134:142:treatment,144:153:treatment | Women who are actively using opioids (i.e., heroin) methamphetamines and/or abusing prescription drugs not prescribed to them (e.g., Dilaudid, Oxycontin) or alcohol dependent (5+ bottles/glasses of alcohol a day) | 3 | [
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