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Clinical Trial Details

Trial ID: L6661
Source ID: NCT00506961
Associated Drug: Rosuvastatin
Title: Evaluate the Efficacy and Safety of Rosuvastatin Versus Simvastatin in Type 2 Diabetic Patients With Dyslipidemia
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes Mellitus|Dyslipidemia
Interventions: DRUG: Rosuvastatin|DRUG: Simvastatin
Outcome Measures: Primary: The percentage of patients achieving the combined treatment goal of LDL-C < 100mg/dl and non-HDL-C < 130 mg/dl at week 12 with rosuvastatin treatment compared with simvastatin treatment, 12 weeks | Secondary: Achieving the combined treatment goal of LDL-C (<100 mg/dL) and non-HDL-C (130 mg/dL) at week 4;, 4 weeks|Percentage of patients achieving the LDL-C goal of <100 mg/dL at week 4 and week 12;, 12 weeks|Percentage of patients achieving the LDL-C goal of <70 mg/dL at Week;The mean percent change from baseline in lipid profile at week 4 and week 12;, 12 weeks
Sponsor/Collaborators: Sponsor: Taipei Veterans General Hospital, Taiwan
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 90
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: HEALTH_SERVICES_RESEARCH
Start Date: 2006-06
Completion Date: 2007-07
Results First Posted:
Last Update Posted: 2011-12-06
Locations: Taichung Veterans General Hospital, Taichung, Taiwan|Taipei Veterans General Hospital, Taipei, Taiwan
URL: https://clinicaltrials.gov/show/NCT00506961