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Clinical Trial Details

Trial ID: L6918
Source ID: NCT00899483
Associated Drug: Glucose Potassium Insulin Solution
Title: Can Enhanced Glycemic Control in Type II Diabetics Improve Myocardial Protection During Coronary Artery Bypass Grafting?
Acronym: GUIDE
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Type 2 Diabetes
Interventions: DRUG: Glucose potassium insulin solution
Outcome Measures: Primary: The difference in the mean left ventricular end-systolic volume index (LVESVI) after CABG and the amount of new permanent injury detected in the late CMRI study, 3 months post CABG | Secondary: Glycaemic control will be assessed 2 hours pre-operatively and 72 hours post-operatively. Measurement timings will be standardized allowing comparison of glycaemic control during different time-periods., 72 hours post CABG
Sponsor/Collaborators: Sponsor: University Hospital Birmingham | Collaborators: British Heart Foundation
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 100
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2009-07
Completion Date:
Results First Posted:
Last Update Posted: 2009-05-12
Locations: University Hospital Birmingham, Birmingham, West Midlands, B15 2TH, United Kingdom
URL: https://clinicaltrials.gov/show/NCT00899483