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NCT03034564 | 1:27:chronic_disease | inflammatory bowel disease | 3 | [
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NCT03079297 | 21:30:allergy_name | Hypersensitivity to L-leucine | 3 | [
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NCT01306045 | 1:25:chronic_disease | Unstable angina pectoris | 3 | [
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NCT02404155 | 30:49:treatment,56:89:treatment,91:115:chronic_disease,117:133:chronic_disease,141:159:chronic_disease,161:180:chronic_disease | Eligible and recommended for clozapine treatment (e.g. treatment resistant schizophrenia, schizoaffective disorder, bipolar disorder, other psychotic disorder, delusional disorder, hostility, other documented rationale) | 3 | [
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NCT01422746 | ,,69:88:chronic_disease | Total testosterone > 150 ng/dL, which suggests the possibility of a virilizing neoplasm | 3 | [
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NCT02531932 | 26:39:treatment,55:71:chronic_disease,,99:109:treatment,208:226:treatment | Patients, who have had a major surgery or significant traumatic injury within 4 weeks of start of study drug, patients who have not recovered from the side effects of any major surgery (defined as requiring general anesthesia) or patients that may require major surgery during the course of the study | 3 | [
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NCT02789111 | 1:20:treatment | Major spine surgery scheduled as part of clinical care | 3 | [
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NCT02562235 | 12:36:chronic_disease,48:64:chronic_disease,68:81:chronic_disease | History of left-sided heart disease, including valvular disease or heart failure | 3 | [
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NCT02577406 | 23:27:treatment,,65:80:treatment,88:123:treatment,181:213:chronic_disease | Subject has undergone HSCT within 60 days prior to the start of study treatment, or on immunosuppressive therapy post HSCT at the time of screening, or with clinically significant graft-versus-host disease (GVHD) | 3 | [
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NCT02748577 | 1:13:chronic_disease,31:43:chronic_disease,45:75:chronic_disease | Chronic pain condition (e.g., fibromyalgia, migraines for healthy controls, etc.) | 3 | [
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NCT02314377 | 1:20:chronic_disease | Atrial fibrillation | 3 | [
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NCT03037931 | 54:75:treatment | Current or planned mechanical circulatory support or heart transplantation | 3 | [
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NCT03007745 | 1:33:chronic_disease | obesity hypoventilation syndrome | 3 | [
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NCT01553071 | ,,25:36:treatment | Hemoglobin ≥ 8.0 gm/dL; transfusion permitted to achieve this level | 3 | [
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NCT03029884 | 57:68:allergy_name,82:90:allergy_name,92:104:allergy_name,106:114:allergy_name,116:130:allergy_name,132:147:allergy_name | Allergies or known hypersensitivity to materials in the Activa PC+S system (i.e. titanium, polyurethane, silicone, polyetherimide, stainless steel) | 3 | [
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NCT02928991 | 1:51:chronic_disease | Uncontrolled bacterial, viral or fungal infections | 3 | [
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NCT01653080 | 1:14:chronic_disease,26:41:chronic_disease,43:59:treatment,61:72:cancer | Renal disease (including solitary kidney, renal transplant, renal tumor) | 3 | [
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NCT03053518 | 36:54:chronic_disease | Chronically active inflammatory or neoplastic disease in the three years prior to enrollment | 3 | [
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NCT02303977 | 23:50:treatment,38:50:treatment,65:76:cancer,70:76:cancer,85:106:treatment,117:124:treatment,167:187:treatment, | Patients who received platinum-based chemotherapy for localized lung cancer (either adjuvant chemotherapy following surgery or chemotherapy given in conjunction with definitive radiation) are eligible if their cancer has recurred within 6 months of platinum-based chemotherapy | 3 | [
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NCT00703105 | 23:35:treatment,39:51:treatment,,80:92:treatment,96:107:treatment | Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier | 3 | [
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NCT02826577 | 1:19:treatment | Psychotropic drugs | 3 | [
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NCT02120222 | 12:20:chronic_disease,22:40:chronic_disease,44:59:chronic_disease, | History of seizures, movement disorders or cerebrovascular accident within the past 5 years | 3 | [
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NCT02911467 | 34:46:treatment | For patients undergoing optional tumor biopsy | 3 | [
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NCT02510417 | ,,41:51:treatment | Steroids less or equal to 0.5 mg/kg/day prednisone | 3 | [
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NCT01539109 | 1:21:chronic_disease | Neurologic condition affecting sensorimotor systems | 3 | [
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NCT02579265 | 1:9:chronic_disease | volvulus | 3 | [
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NCT01174108 | 1:17:chronic_disease | Fanconi s anemia | 3 | [
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NCT02554786 | 12:33:chronic_disease,45:51:chronic_disease,84:88:chronic_disease,90:101:chronic_disease,103:128:chronic_disease,130:145:chronic_disease,170:184:chronic_disease,189:208:chronic_disease | history of chronic lung diseases other than asthma, including (but not limited to) COPD, sarcoidosis, interstitial lung disease, cystic fibrosis, clinically significant bronchiectasis and active tuberculosis | 3 | [
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NCT00720785 | 1:17:cancer,,,115:126:treatment,130:154:treatment,196:220:chronic_disease | Brain metastases (with the exception of patients with a single brain metastasis less than 1cm treated with either sterotactic or gamma knife radiotherapy) due to poor prognosis and potential for neurological dysfunction that would confound evaluation of neurological and other adverse events) | 3 | [
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NCT01898793 | 14:20:chronic_disease,42:65:chronic_disease,94:102:chronic_disease,113:144:chronic_disease | Uncontrolled angina, severe uncontrolled ventricular arrhythmias, or EKG suggestive of acute ischemia or active conduction system abnormalities | 3 | [
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NCT01681264 | 43:55:chronic_disease,59:79:chronic_disease,155:158:treatment | Has other chronic pain conditions such as fibromyalgia or joint osteoarthritis that are predominant over back and neck pain with regard to its intensity (VAS) | 3 | [
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NCT01994382 | 7:42:cancer | Known lymphomatous involvement of the CNS | 3 | [
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NCT02072148 | 4:20:treatment,22:39:treatment,43:55:treatment,60:65:cancer,78:84:treatment,88:101:treatment | No previous surgery, radiation therapy or chemotherapy for SCCHN (other than biopsy or tonsillectomy) is allowed at time of study entry | 3 | [
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NCT02464696 | 10:28:treatment,34:39:chronic_disease,41:51:chronic_disease,55:72:chronic_disease | Risk for gastric aspiration (ie; ileus, esophageal or bowel obstruction, active vomiting) | 3 | [
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NCT02490943 | 1:19:chronic_disease | Cognitive deficits that would interfere with the subject's ability to give informed consent or perform study testing | 3 | [
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NCT02888119 | ,,,32:34:chronic_disease,,, | Patients ages 40-75 with early OA as determined by KL scores 1-2 | 3 | [
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NCT02254863 | 10:13:treatment,15:56:treatment,65:95:treatment | Abnormal EEG, Brainstem Auditory Evoked Response (BAER), and/or Visual Evoked Potentials (VEP) | 3 | [
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NCT00875342 | 21:32:allergy_name | Hypersensitivity to cycloserine | 3 | [
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NCT02595372 | 9:30:treatment,36:49:treatment,54:60:treatment,72:84:treatment | Planned neoadjuvant treatment with anthracycline and taxane containing chemotherapy | 3 | [
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NCT02584309 | 1:12:cancer,14:31:cancer,33:44:cancer,48:64:cancer | Liposarcoma (myxoid/round cell, pleomorphic or dedifferentiated) | 3 | [
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NCT02323191 | 15:40:chronic_disease | History of or active autoimmune disease | 3 | [
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NCT02456857 | 20:49:cancer,,,,,,,,,,, | Confirmed invasive triple-negative breast cancer defined as estrogen receptor (ER) < 10%; progesterone receptor (PR) < 10% by immunohistochemistry (IHC) and human epidermal growth factor receptor 2 (HER2) 0-1+ (by IHC), or 2+ (fluorescence in situ hybridization [FISH] < 2, gene copy number < 4) | 3 | [
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NCT02169037 | 1:20:chronic_disease,30:42:cancer,69:77:treatment | intramural thrombus or other cardiac mass that may adversely effect catheter introduction or manipulation | 3 | [
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NCT01896999 | 22:32:cancer,59:83:cancer,85:111:cancer,119:129:treatment,134:143:treatment | No evidence of prior malignancy except adequately treated non-melanoma skin cancer, in situ cervical carcinoma or any surgically- or radiation-cured malignancy continuously disease | 3 | [
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NCT02512926 | 1:33:treatment | Prior treatment with carfilzomib | 3 | [
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NCT01954576 | 25:28:treatment | Unable to undergo brain MRI due to medical or personal reasons | 3 | [
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NCT01532687 | 29:40:treatment, | subjects may not have had a transfusion within 7 days of screening assessment | 3 | [
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NCT02862938 | 17:25:chronic_disease,54:68:chronic_disease,70:96:chronic_disease,100:119:chronic_disease | Participant has glaucoma that is not considered open angle glaucoma, pseudoexfoliation glaucoma or pigmentary glaucoma | 3 | [
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NCT02167958 | ,,84:92:chronic_disease,,,,, | Remission is defined as < 5% blasts with no morphological characteristics of acute leukemia (e.g., Auer Rods) in a bone marrow with > 20% cellularity, peripheral blood counts showing ANC >1000/ul, including patients in CRp | 3 | [
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NCT02184520 | 28:32:chronic_disease,34:37:chronic_disease,39:50:chronic_disease | Systemic disease including AIDS, HIV, Hepatitis C | 3 | [
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NCT02755116 | 20:42:chronic_disease,50:73:chronic_disease,77:101:chronic_disease,106:125:chronic_disease,136:163:treatment | History of serious ventricular arrhythmia (i.e.: ventricular tachycardia or ventricular fibrillation) or cardiac arrhythmias requiring anti-arrhythmic medications | 3 | [
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NCT01366612 | 14:23:chronic_disease,25:30:chronic_disease,32:38:chronic_disease,42:62:chronic_disease | Uncontrolled bacterial, viral, fungal or parasitic infections | 3 | [
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NCT02233868 | ,,,,,122:130:treatment | Must have had the last drinking episode (females 3 or more drinks; and males 4 or more drinks) within 1 week of baseline PET scan (self-report) | 3 | [
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NCT01059786 | 47:58:treatment,64:73:treatment,81:93:treatment | Patients with history of non-response to both pentostatin plus rituximab and to bendamustine plus rituximab | 3 | [
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NCT02188121 | 47:55:chronic_disease,57:81:chronic_disease,89:107:chronic_disease | Unable to provide informed consent, e.g., has dementia, developmental disability, other cognitive disorder, or fails screening mini-mental status exam (subjects with guardians may participate with guardian consent) | 3 | [
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02841540 | 1:21:chronic_disease | Retinitis Pigmentosa | 3 | [
"Retinitis",
"Pigmentosa"
] | [
2,
2
] |
NCT02303977 | 43:61:treatment | Must have recovered from toxic effects of prior chemotherapy | 3 | [
"Must",
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] | [
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02522715 | 1:13:treatment | Bicalutamide; approximate half-life: 6 days; washout period required: 36 days | 3 | [
"Bicalutamide",
";",
"approximate",
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":",
"6",
"days",
";",
"washout",
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02747888 | 52:73:cancer | Families with a current or previous diagnosis of a thyroid cancer/nodule occurring in childhood | 3 | [
"Families",
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"previous",
"diagnosis",
"of",
"a",
"thyroid",
"cancer/nodule",
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0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3,
0,
0,
0
] |
NCT02252588 | 16:29:treatment, | Current use of chlorhexidine or over-the-counter mouth washes in the last 2 months | 3 | [
"Current",
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"chlorhexidine",
"or",
"over-the-counter",
"mouth",
"washes",
"in",
"the",
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0,
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0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02743377 | 16:19:chronic_disease | Diagnosed with MAS under 98-D-0145 | 3 | [
"Diagnosed",
"with",
"MAS",
"under",
"98-D-0145"
] | [
0,
0,
2,
0,
0
] |
NCT02479698 | ,,,122:153:treatment | Negative pregnancy test in female patients of childbearing potential, defined as not post-menopausal for 12 months or no previous surgical sterilization | 3 | [
"Negative",
"pregnancy",
"test",
"in",
"female",
"patients",
"of",
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",",
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"or",
"no",
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"sterilization"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02332850 | 17:33:treatment | requirement for intravenous (IV) alimentation | 3 | [
"requirement",
"for",
"intravenous",
"(",
"IV",
")",
"alimentation"
] | [
0,
0,
1,
1,
0,
0,
0
] |
NCT02532231 | 13:38:treatment,45:62:treatment,67:78:chronic_disease, | positive by polymerase chain reaction or on antiviral therapy for hepatitis C within the last 6 months | 3 | [
"positive",
"by",
"polymerase",
"chain",
"reaction",
"or",
"on",
"antiviral",
"therapy",
"for",
"hepatitis",
"C",
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"the",
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] | [
0,
0,
1,
1,
1,
0,
0,
1,
1,
0,
2,
2,
0,
0,
0,
0,
0
] |
NCT02004275 | 15:36:chronic_disease, | No history of myocardial infarction within 6 months prior to registration | 3 | [
"No",
"history",
"of",
"myocardial",
"infarction",
"within",
"6",
"months",
"prior",
"to",
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] | [
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT02008136 | 43:69:treatment | History of adverse events associated with botulinum toxin injections | 3 | [
"History",
"of",
"adverse",
"events",
"associated",
"with",
"botulinum",
"toxin",
"injections"
] | [
0,
0,
0,
0,
0,
0,
1,
1,
1
] |
NCT02402660 | 57:92:chronic_disease | Has a clinical diagnosis of typical autosomal recessive Stargardt macular dystrophy (STGD1) | 3 | [
"Has",
"a",
"clinical",
"diagnosis",
"of",
"typical",
"autosomal",
"recessive",
"Stargardt",
"macular",
"dystrophy",
"(",
"STGD1",
")"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
2,
0,
0
] |
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