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NCT01639508 | 36:48:cancer,52:71:cancer,,112:124:treatment | The subject has any evidence of an endotracheal or endobronchial tumor within 28 days before the first dose of cabozantinib | 2 | [
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NCT02155946 | 22:36:chronic_disease | No history of severe mental illness | 2 | [
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NCT03123198 | 92:105:chronic_disease,126:134:chronic_disease,167:197:treatment | Clients who need mental health services not available at the DBT-RU, such as treatment for schizophrenia or life-threatening anorexia, or who are currently obtaining optimum professional treatment that should not be ended | 2 | [
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NCT01547429 | 1:18:chronic_disease | Diabetes mellitus | 2 | [
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NCT02494869 | 1:18:chronic_disease | Mental impairment leading to inability to cooperate | 2 | [
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NCT02723994 | 1:54:treatment | CRLF2 rearrangement with JAK1 or JAK2 mutation (JAK+) | 2 | [
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NCT02547818 | 18:29:treatment | Currently taking medications that could lead to difficulty complying with the protocol | 2 | [
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NCT02323581 | 1:16:chronic_disease | Cardiac disease | 2 | [
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NCT00291525 | 1:20:chronic_disease | Neurological events | 2 | [
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NCT01961557 | 16:23:chronic_disease | A history of a seizure in the past year | 2 | [
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NCT02502799 | 14:44:chronic_disease,,, | Diagnosis of autism spectrum disorder (ASD) with a severity level of 2 or 3 | 2 | [
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NCT02273375 | 20:44:cancer | adequately treated non-melanoma skin cancer | 2 | [
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NCT02353728 | 1:34:chronic_disease | Complete left bundle branch block | 2 | [
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NCT00147056 | 43:58:treatment | Able to communicate sensations during the ExAblate MRGFUS procedure | 2 | [
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NCT01989585 | 29:39:treatment,55:66:treatment,70:88:treatment | Current use of a prohibited medication; the following medications or non-drug therapies are prohibited | 2 | [
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NCT02606396 | 20:43:chronic_disease | Prior diagnosis of oropharyngeal dysphagia | 2 | [
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NCT02272556 | 11:26:chronic_disease | Untreated thyroid disease | 2 | [
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NCT01187368 | 1:33:chronic_disease | Severe right ventricular failure | 2 | [
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NCT02343042 | 18:32:chronic_disease | Active, unstable cardiovascular function | 2 | [
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NCT03139227 | 19:28:treatment,30:40:treatment,56:76:treatment | Concurrent use of tamoxifen, raloxifene, or any of the aromatase inhibitors | 2 | [
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NCT02020707 | ,,,50:69:treatment,, | patients discovered to have >= 2+ proteinuria on dipstick urinalysis at baseline should undergo a 24 hour urine collection and must demonstrate =< 1 g of protein in 24 hours to be eligible | 2 | [
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NCT02484404 | 24:51:chronic_disease,35:51:chronic_disease,99:114:chronic_disease,118:143:chronic_disease | Clinically significant peripheral vascular disease or vascular disease, including rapidly growing aortic aneurysm or abdominal aortic aneurysm | 2 | [
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NCT02124772 | 16:29:treatment | Any prohibited medication(s), currently used or expected to be required | 2 | [
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NCT00573027 | 16:39:chronic_disease,,,86:105:chronic_disease,,142:153:treatment | No obstructive coronary artery disease performed within the previous 24 months (<50% luminal obstruction in one or more coronary arteries on angiography) | 2 | [
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NCT02201992 | 82:100:chronic_disease | if clinically indicated additional imaging studies must be performed to rule out metastatic disease | 2 | [
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NCT03021538 | 1:16:chronic_disease,17:31:chronic_disease,42:51:chronic_disease,115:127:treatment | Cystic fibrosis/bronchiectasis/resistant infection patients where surgeon will need to remove both lungs prior to implantation | 2 | [
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NCT02434809 | 35:45:treatment,47:61:treatment,67:86:treatment,112:136:treatment | Active implanted devices, such as pacemakers, defibrillators, and drug infusion pumps since the effects of the Calypso System operation on these devices are unknown | 2 | [
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NCT02100891 | ,,,,59:90:treatment | Pulmonary: DLCO <40% TLC <40%, FEV1 <40% and/or receiving supplementary continuous oxygen | 2 | [
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NCT02519452 | 70:86:cancer | Participant is exhibiting clinical signs of meningeal involvement of multiple myeloma | 2 | [
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NCT01419561 | 1:13:chronic_disease,, | Coagulopathy (PT or PTT >1.5 times upper limit of normal) | 2 | [
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NCT02502708 | 44:61:cancer,86:96:cancer,98:113:cancer,124:160:cancer | histologically proven initial diagnosis of high-grade glioma (WHO grade III and IV), ependymoma, medulloblastoma, or other primary central nervous system tumor | 2 | [
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NCT02025465 | ,55:68:chronic_disease | A low ejection fraction is not always associated with heart failure | 2 | [
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NCT02189798 | 90:117:treatment | Unrealistic expectations regarding potential benefits, risks and limitations inherent to implant surgical procedures as determined by the investigator | 2 | [
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NCT02128906 | 20:38:chronic_disease | Patients must have measurable disease according to RECIST 1.1 | 2 | [
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NCT02933034 | 19:27:chronic_disease, | have a history of torsades or prolonged QT/QTc interval | 2 | [
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NCT02583893 | 1:28:treatment | Telithromycin (e.g., Ketek) | 2 | [
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NCT02611063 | 1:24:chronic_disease | Active hemolytic anemia | 2 | [
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NCT02665962 | 26:45:cancer,,103:119:treatment,132:154:treatment,158:167:treatment | Diagnosed with any other invasive malignancy currently, in the last five years or expected to undergo active treatment with either cytotoxic chemotherapy or radiation during the 6 week caloric restriction period | 2 | [
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NCT02416102 | 13:29:chronic_disease,41:45:chronic_disease,50:68:chronic_disease,78:92:chronic_disease,97:103:chronic_disease | Concomitant airway disorders other than COPD and chronic bronchitis, such as bronchiectasis and asthma (history and reversible airflow obstruction by American Thoracic Society (ATS) criteria) | 2 | [
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NCT02398773 | ,61:73:treatment,78:88:cancer,,152:194:treatment | Patient must NOT have a history of > 1 line of administered chemotherapy for metastatic disease and must be off chemotherapy for a minimum of 2 weeks; prior chemotherapy in the adjuvant setting is allowed | 2 | [
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NCT02930018 | 139:151:treatment | Intent to use any endovascular device other than a stent retriever or clot aspiration device or intra-arterial medications as the initial thrombectomy approach | 2 | [
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NCT02258438 | 1:7:cancer | cancer | 2 | [
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NCT02202811 | 20:23:chronic_disease,, | Moderate to severe OSA (AHI)>15 | 2 | [
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NCT01366612 | 14:28:cancer | Uncontrolled CNS metastases | 2 | [
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NCT02394535 | 1:29:treatment | Prior abdominal radiotherapy | 2 | [
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NCT02265874 | 38:56:chronic_disease,69:80:treatment,84:107:treatment | patients with extensive irreversible pulmonary fibrosis (based upon lung biopsy or high resolution CT scan criterion) | 2 | [
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NCT02109627 | 1:11:treatment,15:36:treatment,41:44:cancer,50:72:treatment,,116:141:treatment,147:151:chronic_disease, | Allogeneic or autologous transplant for AML with infusion of stem cells within 90 days of study entry or on active immunosuppressive therapy for (GVHD) within 2 weeks before study entry | 2 | [
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NCT02564978 | 21:55:chronic_disease,51:54:chronic_disease,112:122:treatment | Current evidence of choroidal neovascularization (CNV) as determined by the treating physician or a history of treatments for CNV | 2 | [
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NCT02496663 | 35:47:treatment,,62:74:treatment,,105:116:treatment | Patients must have completed last chemotherapy >= 3 weeks or radiotherapy >= 2 weeks prior to receiving study drugs | 2 | [
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NCT01948739 | 32:38:chronic_disease | No previous clinically defined stroke | 2 | [
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NCT02091141 | 33:46:chronic_disease,87:102:treatment,137:147:treatment | Refractory nausea and vomiting, malabsorption, external biliary shunt, or significant bowel resection that would preclude absorption of vismodegib | 2 | [
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NCT00630253 | ,,,44:66:chronic_disease, | In patients 18-60 years of age, moderately severe aplastic anemia is defined as having at least one | 2 | [
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NCT02206945 | 30:33:chronic_disease,, | Primary Diagnosis of Current OCD, based on Diagnostic and Statistical Manual (DSM-IV) criteria, a Y-BOCS (Yale-Brown Obsessive-Compulsive Scale) score >=16 | 2 | [
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NCT01773707 | 38:51:chronic_disease | Have serological evidence of current CMV infection | 2 | [
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NCT01626079 | 36:58:treatment,36:45:treatment,132:134:treatment | Leaflet anatomy which may preclude MitraClip implantation, proper MitraClip positioning on the leaflets or sufficient reduction in MR by the MitraClip | 2 | [
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NCT02338999 | ,43:52:treatment,, | Postmenopausal women who have undergone a DEXA scan during the last year and have a T score better than -2.5 will be included without repeating the DEXA scan prior to enrollment | 2 | [
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NCT02252432 | 1:25:chronic_disease,27:45:chronic_disease,47:64:chronic_disease | Restrictive lung disease (pulmonary fibrosis, myasthenia gravis) | 2 | [
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NCT02607033 | 8:14:cancer | Active cancer | 2 | [
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NCT02140554 | 14:39:chronic_disease | Diagnosis of sickle cell disease (SCD), with either βS/βS or βS/β0 or βS/β+ genotype | 2 | [
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NCT01877382 | ,,42:45:treatment | > 470 ms for females based on triplicate ECG | 2 | [
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NCT01670877 | 14:34:chronic_disease,77:93:chronic_disease,95:119:chronic_disease,121:139:chronic_disease,144:181:chronic_disease | Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements | 2 | [
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NCT01101451 | 15:28:cancer,60:69:treatment,73:85:treatment | Patients with cervix cancer who have received any previous radiation or chemotherapy | 2 | [
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NCT01379573 | 81:84:chronic_disease | Identification of any of the following structural lesions considered causal for CHB, i.e., those that could account for block because of fibrous disruption between the atrium and AV node or due to absence of the penetrating bundles of the AV node | 2 | [
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NCT03179163 | ,42:69:treatment | Women are post-menopausal and not taking hormone replacement therapy | 2 | [
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NCT02488967 | 1:4:chronic_disease,,,, | ISH non-amplified with a ratio of HER2 to CEP17 < 2.0, and if reported, average HER2 gene copy number < 4 signals/cells | 2 | [
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NCT03148795 | 36:50:chronic_disease | Patients must have measurable soft tissue disease per RECIST 1.1 | 2 | [
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NCT02366754 | 1:23:chronic_disease | Traumatic Brain Injury etiology | 2 | [
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NCT02176967 | 20:45:cancer | Only patients with MYCN non-amplified tumors | 2 | [
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NCT03179397 | 1:24:chronic_disease | Iris Neovascularization | 2 | [
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NCT01943851 | 43:46:cancer,48:50:cancer,55:58:cancer | In Part 1 and, Part 2, subjects must have AML, MM, or NHL | 2 | [
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NCT02048722 | 1:31:chronic_disease | Active coronary artery disease | 2 | [
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NCT02349867 | 1:20:chronic_disease | Arterial thrombotic | 2 | [
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NCT01582191 | ,57:79:treatment,,185:201:treatment,277:294:treatment,296:330:treatment,415:424:treatment | Patients must be at least 3 weeks beyond their previous cytotoxic chemotherapy; patient must be at least 5 half-lives or 3 weeks, whichever is shorter, from their previous targeted or biologic therapy; in addition, patients must be at least 3 weeks beyond the last session of radiation therapy; local palliative radiatio... | 2 | [
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NCT02355535 | 1:54:treatment | Prior allogeneic bone marrow or organ transplantation | 2 | [
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NCT02562235 | 14:17:chronic_disease,31:64:treatment,60:63:treatment,,157:170:treatment | Diagnosis of PAH confirmed by right heart catheterization (RHC) at any time prior to enrolment (for patients with closed shunts - RHC no less than 4 months after surgery) | 2 | [
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NCT02513225 | ,48:65:chronic_disease, | At least one episode of binge substance use or suicidal ideation recorded in the Apache community-based surveillance system in the past 90 days | 2 | [
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NCT02680535 | 1:37:chronic_disease,,,,,,,,, | acute or chronic hepatic dysfunction as evidenced by clinically significant abnormalities in albumin, total protein, or prothrombin time, or evidence of hepatic injury with clinically important (> grade 1) changes in AST, ALT, ALP, bilirubin, or GGT values | 2 | [
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NCT03137173 | 12:44:treatment, | Use of any systemic antibacterial treatment within 14 days | 2 | [
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NCT03001830 | 8:26:chronic_disease | severe bleeding phenotype | 2 | [
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NCT02577406 | 32:47:chronic_disease,,86:101:treatment,,,,163:187:chronic_disease | Subject has significant active cardiac disease within 6 months prior to the start of study treatment, including New York Heart Association (NYHA) class III or IV congestive heart failure | 2 | [
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NCT02834403 | 5:37:chronic_disease, | Any medical or psychiatric condition that would prevent informed consent or limit expected survival to less than 4 weeks | 2 | [
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NCT03151083 | 16:24:chronic_disease, | Diagnosed with insomnia lasting 3 months by the PACT provider, as evidenced by referral by the provider for access to the SHUTiTM program | 2 | [
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NCT02660528 | 1:10:chronic_disease | hypomania | 2 | [
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NCT02589938 | 21:36:cancer | have a diagnosis of head/neck cance | 2 | [
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NCT03171168 | 20:45:treatment, | Patient started on lipid lowering medication in last 3 months | 2 | [
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NCT02502799 | 14:30:chronic_disease,32:45:chronic_disease,60:78:chronic_disease | Diagnosis of bipolar disorder, schizophrenia, and/or other psychotic disorder | 2 | [
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NCT01604512 | 25:56:treatment | Any contraindication to gadolinium intravenous contrast as per standard Department of Radiology contrast guidelines | 2 | [
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NCT02321501 | 1:38:treatment | enzyme-inducing anticonvulsive agents | 2 | [
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NCT02819440 | 1:8:chronic_disease,, | Obesity (BMI ≥ 30 kg/m2) | 2 | [
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NCT02148003 | 21:24:treatment, | History of previous RFA at the same level(s) in the previous 12 months | 2 | [
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NCT03040726 | 23:39:treatment,43:58:treatment,63:74:treatment | Expected to use other 5HT3 antagonists or NK1 antagonists for prophylaxis during the study | 2 | [
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NCT02525692 | ,41:56:treatment,58:70:treatment,72:84:treatment,93:100:treatment,131:139:chronic_disease | All adverse events Grade > 1 related to prior therapies (chemotherapy, radiotherapy, and/or surgery) must be resolved, except for alopecia | 2 | [
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NCT03006302 | 1:33:treatment,35:44:treatment,46:56:treatment,61:71:treatment,81:94:treatment | Prior treatment with anti-CTLA-4, anti-PD-1, anti-PD-L1, or anti PD-L2, or with IDO inhibitor | 2 | [
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NCT02520778 | 11:26:treatment,30:51:treatment,84:100:chronic_disease,106:116:treatment | receiving anticoagulation or anti-platelet therapy are excluded due to the risk of thrombocytopenia with navitoclax | 2 | [
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NCT02503722 | ,,,51:64:chronic_disease | New York Heart Association (NYHA) class III or IV heart failure | 2 | [
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NCT02293096 | 1:23:chronic_disease | end stage liver disease | 2 | [
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NCT02929589 | 85:94:allergy_name,96:105:allergy_name,110:134:allergy_name | Those patients who are allergic to, refuse to take, or are otherwise unable to take oxycodone, ibuprofen, or acetaminophen medication orally for post-operative pain management | 2 | [
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NCT02685605 | 1:21:chronic_disease | Supratentorial T1-Gd enhancing lesion(s) amenable to total resection | 2 | [
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NCT02465060 | 92:105:chronic_disease,118:134:chronic_disease,174:198:chronic_disease | No factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death | 2 | [
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