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NCT02181257 | ,144:147:chronic_disease, | Frequent laboratory based spirometry defined as having had regular FEV1 measurements during the preceding six months prior to diagnosis of new BOS with no time interval between FEV1 measurements that exceeds 8 weeks | 2 | [
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NCT02804230 | 34:59:chronic_disease, | Patients with a known history of psychogenic non-epileptic spells in the last three years | 2 | [
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NCT01962415 | 1:29:treatment,,,,,, | Pulmonary evaluation testing demonstrating CVC or FEV1/FVC of ≥ 50% of predicted for age and/or resting pulse oximeter ≥ 92% on room air or clearance by the pediatric or adult pulmonologist | 2 | [
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NCT02562430 | 5:38:treatment | Any investigational psychotropic drug within the last year | 2 | [
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NCT00967577 | 56:77:cancer,79:89:cancer,91:104:cancer,106:112:cancer,114:133:cancer,135:145:cancer,147:155:cancer,157:162:cancer,164:173:cancer,178:185:cancer | This will include, but is not limited to patients with cancers of the kidney, urothelium, head and neck, breast, non-small cell lung, colorectal, pancreas, ovary, esophagus and gliomas | 2 | [
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NCT02041936 | 29:50:treatment | Unable to be treated with a muscle blockade agent | 2 | [
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NCT01986205 | ,161:169:chronic_disease,281:291:chronic_disease,293:300:chronic_disease,302:323:chronic_disease | At least 3 of the following persistent symptoms from the injury: headaches, dizziness or balance problems, blurred vision, tiredness/fatigue or sleep problems, seizures, remembering things or solving problems, managing stress or emotional upsets, controlling temper/irritability, depression, anxiety, post-traumatic stre... | 2 | [
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NCT01028846 | 1:21:chronic_disease | hypercholesterolemia | 2 | [
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NCT02360579 | 21:53:treatment | Patients who are on chronic systemic steroid therapy for any reason | 2 | [
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NCT02620449 | 9:16:chronic_disease,, | extreme obesity (BMI ≥ 35 kg/m2) | 2 | [
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NCT02987491 | ,,,,54:59:chronic_disease,, | Normal weight (body mass index [BMI] 18-26 kg/m2) or obese (BMI 30-46 kg/m2) | 2 | [
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NCT02809677 | 1:27:chronic_disease,37:43:chronic_disease,45:61:chronic_disease,63:76:chronic_disease | severe psychiatric illness, such as autism, bipolar disorder, schizophrenia or current drug/alcohol abuse/dependence | 2 | [
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NCT03077243 | 1:38:chronic_disease,61:80:chronic_disease,127:134:treatment | Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration | 2 | [
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NCT02682407 | 1:12:chronic_disease | hepatitis C infection | 2 | [
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NCT02682147 | 14:20:chronic_disease | Diagnosis of asthma | 2 | [
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NCT02425904 | 45:80:treatment,96:99:chronic_disease,126:135:treatment,141:155:treatment,157:160:chronic_disease,226:257:treatment | In stratum 1, patients must have failed one prior systemic chemotherapy regimen. In stratum 2, RDD patients must have failed treatment with corticosteroid. ECD patients who have confirmed BRAF V600E mutation must have failed treatment with a BRAF inhibitor or are not considered to be eligible for such treatment | 2 | [
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NCT02512718 | 1:16:chronic_disease | Lipid nephrosis | 2 | [
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NCT01614990 | 1:15:chronic_disease | Claustrophobia (this would make lying in the scanner very uncomfortable) | 2 | [
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NCT01620216 | ,59:73:treatment | a result is available within 2 weeks of starting on study drug treatment | 2 | [
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NCT01128816 | 16:19:treatment,23:27:treatment,31:60:treatment,65:74:treatment,78:89:chronic_disease,110:133:treatment,,178:187:treatment | Current use of ASV or CPAP or mandibular advancement device for treatment of sleep apnea or treated with any investigational therapy during the last 4 weeks (including approved therapies being used in unapproved indications) | 2 | [
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NCT02585791 | 15:36:chronic_disease,58:78:treatment,86:97:treatment, | Subjects with respiratory infection that required use of oral corticosteroids and/or antibiotics within the prior 3 months | 2 | [
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NCT02568267 | 1:25:treatment | Prior anticancer therapy | 2 | [
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NCT00720785 | 1:29:chronic_disease | Active Hepatitis B infection (Hep B surface antigen positive) | 2 | [
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NCT02522494 | 1:9:chronic_disease | Dementia | 2 | [
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NCT03138512 | 52:73:chronic_disease | Any severe or serious, acute or chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation | 2 | [
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NCT02036853 | 31:43:treatment | Patients are able to tolerate triheptanoin if they have been (or are currently being) treated with this medication | 2 | [
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NCT02324582 | 1:31:chronic_disease | active urinary tract infection | 2 | [
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NCT03013543 | 226:233:chronic_disease | Bi-allelic, homozygous or compound heterozygous (a different gene mutation on each allele) genetic status for either the POMC, PCSK1, or LEPR genes, with the loss-of-function (LOF) variant for each allele conferring a severe obesity phenotype | 2 | [
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NCT03090607 | 8:26:treatment | Had an ablation procedure in the lower esophageal sphincter area | 2 | [
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NCT01969643 | 38:49:allergy_name | Combination Arm: hypersensitivity to trastuzumab | 2 | [
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NCT01421095 | ,41:61:treatment | A minimum of 1 year since completion of gonoadotoxic therapy | 2 | [
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NCT02249520 | 40:49:treatment | Outpatient undergoing standard-of-care 18FDG-PET at S. Mark Taper Foundation Imaging Center at CSMC | 2 | [
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NCT02101034 | 15:28:chronic_disease,33:55:treatment,90:105:treatment | patients with HIV infection and antiretroviral therapy are not excluded, as there are no pharmacokinetic tests being performed | 2 | [
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NCT02283333 | 23:40:chronic_disease | Individuals with both suicidal ideation and clear intent | 2 | [
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NCT02793921 | 36:49:cancer | Diagnosed with Stage 0, 1, 2 or 3a Breast Cancer | 2 | [
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NCT02918981 | 14:18:allergy_name | Allergies to milk consumption | 2 | [
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NCT02914171 | 16:22:cancer | history of any cancer | 2 | [
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NCT02366611 | 11:41:treatment | Use of an investigational drug or device | 2 | [
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NCT01241708 | 32:47:treatment | Recovery from complications of prior therapies | 2 | [
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NCT01928576 | 23:76:treatment,69:76:treatment,78:91:treatment,99:116:treatment,145:163:cancer,,223:259:treatment | Patients who received adjuvant or neoadjuvant platinum-doublet chemotherapy (after surgery and/or radiation therapy) and developed recurrent or metastatic disease within 6 months of completing therapy are eligible and the adjuvant or neoadjuvant chemotherapy will count as a line of therapy as above | 2 | [
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NCT02403193 | 22:38:chronic_disease,42:58:chronic_disease,146:155:treatment | Serious uncontrolled medical disorder or active infection that in the investigator's opinion would impair the patient's ability to receive study treatment | 2 | [
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NCT01130077 | 30:48:cancer,50:77:cancer,81:92:cancer | Eligible histologies include glioblastoma (GBM), anaplastic astrocytoma (AA) or gliosarcoma | 2 | [
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NCT02568267 | 1:16:treatment,34:53:treatment,55:59:treatment,64:78:treatment,100:106:cancer | Prior treatment with approved or investigational Trk, ROS1, or ALK inhibitors in patients who have tumors that harbor those respective gene rearrangements | 2 | [
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NCT01366612 | 27:30:treatment | Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant | 2 | [
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NCT02335242 | 202:258:chronic_disease,299:307:chronic_disease,309:321:chronic_disease,323:346:chronic_disease,351:365:chronic_disease,384:397:chronic_disease,399:414:chronic_disease,419:434:chronic_disease | any significant cardiovascular risk factors and any condition which requires participants to use nitric oxide donors or nitrates in any form, underlying anatomic or vascular risk factor for developing non-arteritic anterior ischemic optic neuropathy (NAION) including low ocular cup to disc ratio, diabetes, hypertension... | 2 | [
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NCT01306045 | 20:38:chronic_disease,65:71:treatment,76:95:treatment | Patients must have biopsiable disease and be willing to undergo biopsy for molecular profiling | 2 | [
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NCT02912572 | 20:39:cancer | POLE-mutated, i.e. endometrial cancers known to harbor mutations in the exonuclease domain (amino acid residues 268-471) of polymerase e (POLE) as determined by targeted sequencing or other next generation sequencing assay | 2 | [
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NCT03132415 | 11:15:chronic_disease | Not be on PrEP at time of enrollment | 2 | [
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NCT02354703 | 12:28:chronic_disease | History of Long QT Syndrome or a first-degree biological family member with this condition | 2 | [
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NCT03144245 | 1:10:chronic_disease,12:17:chronic_disease,19:26:chronic_disease,28:44:chronic_disease,46:58:chronic_disease,62:81:chronic_disease | Pulmonary, renal, hepatic, gastrointestinal, neurological or psychiatric disease that would limit compliance with study requirements | 2 | [
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NCT02660528 | 18:44:chronic_disease,58:68:chronic_disease,70:80:chronic_disease,82:91:chronic_disease,97:111:chronic_disease | Patients with an active or recent infection, for example cellulitis, bacteremia, pneumonia, and pyelonephritis | 2 | [
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NCT00887146 | 70:82:treatment | Tissue must have been determined to have local 1p/9q co-deletion and IDH mutation prior to submission for central path review | 2 | [
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NCT02615249 | 1:58:treatment, | Treatment with ultraviolet (UV) light (including tanning) during the 3 weeks prior to inclusion in this study | 2 | [
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NCT02459119 | 22:28:cancer, | Subjects surviving a cancer that was curatively treated and without evidence of disease for more than 3 years before randomization | 2 | [
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NCT02122172 | 41:63:treatment | Patients may not be receiving any other investigational agents | 2 | [
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NCT02253316 | ,,,267:279:treatment | This is defined as either committing to continued abstinence from heterosexual intercourse or beginning TWO acceptable methods of contraception (one highly effective method and one additional effective method AT THE SAME TIME) at least 28 days prior to the start of lenalidomide, for the duration of study participation,... | 2 | [
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NCT02359864 | 30:36:cancer,44:68:cancer | The patient has a history of cancer except non-melanoma skin cancer | 2 | [
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NCT01696734 | 18:29:allergy_name | Known allergy to domperidone | 2 | [
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NCT02109627 | 1:42:cancer | Acute promyelocytic leukemia (FAB M3 AML) | 2 | [
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NCT02477839 | ,105:114:treatment | device settings must be kept stable for >=2 weeks prior to Visit 1 and kept stable during the Baseline, Treatment, and Transition Periods | 2 | [
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NCT02332291 | 1:26:treatment, | Electroconvulsive therapy in last 6 months | 2 | [
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NCT02837510 | 28:44:chronic_disease, | subjects with a history of major depression but in remission for past 6 months are eligible | 2 | [
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NCT02114229 | 4:31:treatment,33:50:treatment,54:66:treatment,90:105:treatment | No previous anticancer therapy (radiation therapy or chemotherapy) other than the use of corticosteroids | 2 | [
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NCT02101944 | 13:44:cancer | Presence of clonal bone marrow plasma cells | 2 | [
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NCT02524275 | 7:17:cancer,49:59:cancer,63:98:cancer,103:117:cancer | Prior malignancy, except for adequately treated basal cell or squamous cell carcinoma of the skin, or thyroid cancer | 2 | [
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