APPROACH
The study is a factorial, multicentre, randomised controlled trial. 11,140 participants have been recruited and randomised to either a fixed low-dose perindopril-indapamide combination or matching placebo, and to either an intensive modified-release gliclazide-based glucose lowering regimen or standard guidelines-based glucose lowering therapy. Follow-up will be for an average of four and a half years. The primary outcomes will be major macrovascular complications (stroke and heart attack) and major microvascular complications (eye and renal disease).
BENEFITS
RESULTS
The trial has completed recruitment on schedule and has now entered the follow-up phase. Final results are expected to be available in 2006. Major sub-studies examining the eye and heart in detail are also under way.
STUDENTSHIP (PhD – join research) |