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Clinical Trial Summary

Subjects with impaired glucose tolerance will be randomized to either rosiglitazone or placebo for a 18 month period. The study will look at baseline, 12 month and 18 month data for exercise tolerance, coronary artery calcification and diabetes indicators.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00733174
Study type Interventional
Source Denver Research Institute
Contact Stacey Mitchell, BSN, RN
Phone 303-399-8020
Email stacey.mitchell@va.gov
Status Recruiting
Phase Phase 4
Start date March 2004

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