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NCT02393690 | 132:152:cancer | Modification of the RECIST v1.1 measurable disease criteria includes a change in the definition of what is considered a measurable malignant lymph node | 2 | [
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NCT02690116 | 26:32:chronic_disease | Currently diagnosed with anemia (fatigue-related factor) | 2 | [
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NCT02951455 | 7:27:chronic_disease, | Gross cognitive impairment as measured by the Mini Mental State Exam | 2 | [
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NCT02390752 | ,39:60:treatment,62:84:treatment,89:107:treatment,111:121:cancer | greater than or equal to 14 days from whole brain radiation, craniospinal radiation, or targeted radiation to CNS tumors | 2 | [
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NCT02560766 | 12:50:chronic_disease, | History of suicidal behavior or suicidal ideation as indicated by the C-SSRS, administered at screening, and as per investigator's judgment | 2 | [
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NCT02387905 | 25:40:chronic_disease | Patients who have frank mechanical pain | 2 | [
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NCT02484404 | 7:25:chronic_disease,36:55:chronic_disease,60:74:chronic_disease,116:125:treatment,131:145:treatment | Prior cardiac arrhythmia including atrial fibrillation and atrial flutter, or requiring concurrent use of drugs or biologics with pro-arrhythmic potential | 2 | [
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NCT02826577 | 1:14:chronic_disease | schizophrenia | 2 | [
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NCT02390752 | 65:83:treatment | Patients must have relapsed after or be refractory to effective standard therapies | 2 | [
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NCT02481245 | 22:33:treatment | Agrees not to change medications during the study | 2 | [
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NCT02132598 | ,,87:102:treatment | The subject has not recovered to baseline or CTCAE ≤ Grade 1 from toxicity due to all prior therapies | 2 | [
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NCT02408861 | 48:57:treatment,62:65:chronic_disease,62:75:chronic_disease,87:113:treatment | Participants MUST receive appropriate care and treatment for HIV infection, including antiretroviral medications when clinically indicated, and should be under the care of a physician experienced in HIV management | 2 | [
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NCT01421095 | 1:24:treatment | unilateral oophorectomy | 2 | [
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NCT02074436 | 1:17:cancer,, | Thrombocytopenia with untransfused platelet counts < 20 x 10⁹/L in the out-patient or in the in-patient setting | 2 | [
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NCT02779556 | 1:22:chronic_disease | cognitive impairments | 2 | [
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NCT02369770 | 1:32:chronic_disease | Severe cardiovascular disorders that interfere with ability to perform moderate movement exercises | 2 | [
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NCT02480114 | 14:24:treatment | Currently on gabapentin | 2 | [
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NCT02235857 | 1:20:chronic_disease,42:53:chronic_disease,55:70:chronic_disease,72:110:chronic_disease,115:131:chronic_disease | Cardiac impairments such as uncontrolled arrhyth¬mia, unstable angina, decompensated congestive heart failure, or valvular disease | 2 | [
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NCT02775162 | 47:62:treatment,64:78:treatment,80:97:treatment,99:124:treatment | requiring all of the following at the time of transplantation: oxygen therapy, inotropic support, renal replacement therapy | 2 | [
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NCT01627301 | 1:10:treatment,16:27:treatment,76:85:treatment,87:100:treatment,102:116:treatment | treatment with medications known to affect the sympathetic nervous system (clonidine, beta blockers, ACE inhibitors) | 2 | [
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NCT01787682 | 8:64:treatment, | Use of protein or amino acid containing nutritional supplements within 5 days of first study day | 2 | [
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NCT02496585 | ,44:65:chronic_disease | Newly diagnosed clinical grade 2 or higher radiation pneumonitis according to CTCAE version 4.0 criteria | 2 | [
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NCT02516670 | 10:28:treatment,33:51:cancer,55:91:cancer,116:141:cancer, | Have had prior chemotherapy for metastatic disease in castration-resistant prostate cancer (prior chemotherapy for hormone-sensitive disease, more than twelve months prior to registration, is acceptable) | 2 | [
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NCT00871260 | 1:41:chronic_disease | Acute ST-elevation myocardial infarction | 2 | [
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NCT01505569 | 1:15:cancer | Hepatoblastoma - metastatic at time of diagnosis and/or relapsed after therapy | 2 | [
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NCT02926248 | ,41:60:treatment | Patients with less than 10 degrees of a flexion contracture | 2 | [
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NCT02261519 | 15:35:treatment, | The subject's anti-EPS medications dose or regimen has changed within 2 weeks prior to screening | 2 | [
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NCT02594501 | ,,52:58:chronic_disease,62:77:chronic_disease,81:87:chronic_disease,96:106:chronic_disease,131:151:treatment,168:187:chronic_disease,,, | Patients older than age 18 with ischemic symptoms (stable or unstable angina or NSTEMI without thrombosis of the target lesion on coronary angiography) or evidence of myocardial ischemia in the presence of ≥ 50% de novo stenosis located in native coronary vessels (max. 2 lesions in one or 2 separate vessels) | 2 | [
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NCT01787409 | 1:33:cancer | Enteropathy-type T-cell lymphoma | 2 | [
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NCT02454010 | 9:26:chronic_disease, | Serious cardiac condition within the last 6 months | 2 | [
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NCT03096886 | 1:39:treatment | Centrally acting antiadrenergic agents | 2 | [
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NCT01791543 | 8:32:treatment,70:80:chronic_disease,93:97:chronic_disease | Failed prior VT or PVC ablation due to spontaneous recurrence of the arrhythmia or frequent PVCs | 2 | [
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NCT01876511 | 31:50:treatment,52:72:treatment,74:84:treatment,105:127:treatment,129:153:treatment,161:186:treatment,205:229:treatment, | received any of the following concomitant therapy: Interleukin-2 (IL-2), interferon, or other non-study immunotherapy regimens, immunosuppressive agents, other investigational therapies or chronic use of systemic corticosteroids within one week prior to first dose of study drug | 2 | [
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NCT00075387 | 35:71:chronic_disease | Subjects with rapidly progressing central nervous system (CNS) disease with associated neurological deterioration | 2 | [
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NCT01591356 | 49:55:cancer | this may be one of the lesions mentioned above; tumors within a previously irradiated field will be designated as 'non-target' lesions | 2 | [
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NCT02962557 | 11:14:chronic_disease,,, | Suspected OSA will be defined as a patient with a screening questionnaire (STOP-Bang) score of 5-8 (A score consistent with a high risk of OSA) | 2 | [
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NCT01696734 | ,,84:95:treatment, | have a negative urine pregnancy test within 30 days of the first administration of domperidone and must either commit to continued abstinence from heterosexual intercourse or use an effective method of birth control during the course of the study) | 2 | [
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NCT01619761 | 1:35:cancer,78:87:treatment,113:122:treatment,145:152:treatment | Acute lymphoblastic leukemia (ALL): induction failure, primary refractory to treatment (do not achieve complete remission after first course of therapy) or are beyond first remission including second or greater remission or active disease | 2 | [
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NCT02526511 | 15:33:cancer,52:69:treatment,77:99:treatment,185:194:treatment | Patients with metastatic disease may have received prior nephrectomy and/or prior systemic therapy (no limit on number); their baseline pMRI would be performed prior to starting a new treatment | 2 | [
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NCT02555280 | 1:11:chronic_disease,43:53:chronic_disease,157:196:treatment | Osteopenia: A screening questionnaire for osteopenia, SCORE (Simple Calculated Osteoporosis Risk Estimation), will be used to screen patients who require a DEXA (dual-energy x-ray absorptiometry) bone mineral density measurement | 2 | [
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NCT02072356 | 1:30:chronic_disease | Active uncontrolled infection | 2 | [
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NCT02169037 | 1:25:chronic_disease | structural heart disease of clinical significance | 2 | [
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NCT02500381 | 21:30:treatment,46:68:treatment,81:92:treatment, | Current or previous treatment with any other experimental treatment (other than deflazacort) within 12 weeks prior to Week 1 | 2 | [
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NCT03059888 | 26:32:cancer | Subject has a history of cancer in the last 5 years | 2 | [
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NCT01861106 | 1:14:chronic_disease | HIV infection | 2 | [
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NCT01986205 | 1:15:chronic_disease | Claustrophobia precluding chamber or hood tolerance | 2 | [
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NCT02567266 | ,,145:161:chronic_disease,169:197:chronic_disease,199:212:chronic_disease,214:230:chronic_disease,232:259:chronic_disease,264:283:chronic_disease,291:316:chronic_disease,318:348:chronic_disease,357:376:chronic_disease | Evidence of clinically significant symptoms will be defined as a Clinical Severity Rating (CSR) greater than or equal to 4 on any DSM-5 defined anxiety disorder (e.g., generalized anxiety disorder, social phobia, selective mutism, separation anxiety disorder) or depressive disorder (e.g., major depressive disorder, per... | 2 | [
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NCT02070549 | 1:42:treatment,12:21:treatment,27:42:treatment,121:134:treatment,192:204:chronic_disease,251:263:chronic_disease | Concurrent treatment with bisphosphonates is permitted; however, treatment must be initiated prior to the first dose of study therapy; prophylactic use of bisphosphonates in patients without bone disease is not permitted, except for the treatment of osteoporosis | 2 | [
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NCT00819208 | 143:149:cancer | Able (i.e., sufficiently fluent) and willing to effectively communicate with the physical activity consultant affiliated with the originating cancer center | 2 | [
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NCT02535312 | 31:40:treatment | Arm A dose level 4 (75 mg/m^2 cisplatin) | 2 | [
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NCT02454517 | 35:55:chronic_disease | Doctor of medicine (MD) confirmed cognitive impairment | 2 | [
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NCT01625923 | 62:72:treatment,83:91:treatment,93:102:treatment,104:111:treatment,113:126:treatment,128:139:treatment,156:166:treatment,183:199:treatment,201:209:treatment,214:230:treatment,277:284:treatment,288:297:treatment | Subjects who are taking drugs that potentially interact with olanzapine including diazepam, lorazepam, alcohol, carbamazepine, fluvoxamine, olanzapine and fluoxetine in combination, CNS acting drugs, levodopa and dopamine agonist, and olanzapine when used in combination with lithium or valproate | 2 | [
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NCT01737502 | 1:26:cancer | localized prostate cancer | 2 | [
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NCT02046330 | ,93:108:treatment, | Adequate trials (equal or >6 weeks at the maximum recommended or tolerated dose) of primary antidepressants from at least 3 different classes | 2 | [
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NCT02743494 | 16:43:cancer | Diagnosed with Stage IV resectable disease | 2 | [
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NCT01584076 | 12:51:treatment | history of prior amblyopia treatment with patching | 2 | [
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NCT03028831 | 1:20:treatment | previous GI surgery resulting in disturbed gut function due to of loss of bowel or altered anatomy | 2 | [
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NCT02324439 | 1:9:treatment,66:79:chronic_disease,81:116:chronic_disease,118:127:chronic_disease,129:143:chronic_disease,147:152:chronic_disease,154:183:chronic_disease | Flaxseed supplementation may be contraindicated in patients with acute abdomen, esophageal stricture or perforation, dysphagia, GI obstruction or ileus, acute intestinal inflammation or unexplained abdominal pain. Patients with any of these conditions will be excluded from this trial as the high fiber content of flaxse... | 2 | [
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NCT01572480 | 16:26:chronic_disease,60:86:chronic_disease,91:106:treatment | Has refractory GI disease with refractory nausea/vomiting, inflammatory bowel disease, or bowel resection that would prevent absorption | 2 | [
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NCT01059786 | 30:39:chronic_disease | Presence of active untreated infection | 2 | [
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NCT03166371 | 1:22:chronic_disease,,,,,, | Acute hepatic failure during current hospitalization with total serum bilirubin > 3.5 mg/dL or transaminase values [alanine transaminase (ALT) and/or aspartate transaminase (AST) values > 3-fold the upper limit of normal range] | 2 | [
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NCT02646930 | 13:62:treatment | Patients on monoclonal antibody preparations directed to TNFα | 2 | [
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NCT02994043 | 55:76:chronic_disease,88:111:chronic_disease,113:127:chronic_disease,133:142:chronic_disease | Currently taking any medications for the treatment of psychiatric disorders, including substance use disorders, mood disorders, and psychosis | 2 | [
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NCT02041936 | 19:31:treatment,36:52:treatment,,89:98:treatment,108:124:treatment | Inability to stop antiplatelet and coumadin therapy for 7 days prior to and 7 days post treatment with the NanoKnife System | 2 | [
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NCT01851369 | 11:17:cancer, | Any other cancer from which the patient has been disease-free for three years | 2 | [
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NCT02863809 | 48:62:treatment | No or minimal tear production with evidence of keratinization of the bulbar conjunctiva | 2 | [
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NCT02151175 | 19:27:chronic_disease,57:74:chronic_disease,90:110:chronic_disease | Subjects who have seizures secondary to drugs, alcohol, metabolic illness or progressive degenerative disease | 2 | [
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NCT02163434 | 117:134:chronic_disease,136:148:chronic_disease,150:163:chronic_disease,168:188:chronic_disease | Felt by the patient's obstetrician or emergency room attending physician not to have other medical problems such as bowel obstruction, pancreatitis, biliary colic, or peptic ulcer disease that could be contributing to the patient's symptoms | 2 | [
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NCT02332187 | 18:26:treatment,,,, | Use of high dose pressors (more than 15 mcg/min of norepinephrine or more than 15 mg/kg/min of dopamine) | 2 | [
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NCT02321501 | 17:33:treatment | Able to swallow oral medications | 2 | [
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NCT01584076 | 7:29:chronic_disease | Known psychological problems | 2 | [
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NCT02025465 | 9:36:chronic_disease,, | Current Atrioventricular (AV) block (2nd or 3rd degree) | 2 | [
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NCT01962415 | 1:8:chronic_disease | Chediak | 2 | [
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NCT03113695 | 1:31:chronic_disease | fungal infections of nail beds | 2 | [
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NCT02124772 | ,,61:75:treatment,120:138:chronic_disease,139:147:chronic_disease | abnormal cardiac valve morphology (>=grade 2) documented by echocardiogram (subjects with grade 1 abnormalities [i.e., mild regurgitation/stenosis] | 2 | [
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NCT02944825 | ,,115:128:chronic_disease | We anticipated enrolling a study population of approximately 60% men and 40% women based on a higher incidence of kidney stones among men in NHANES data | 2 | [
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NCT02822001 | ,54:70:treatment | Patients weighing ≥ 80 pounds who are not -intubated prior to surgery | 2 | [
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NCT00903266 | 24:30:chronic_disease | right-handed (prior to stroke) | 2 | [
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