drugset / Trial / NCT00125593

Summary

The chief aim of SHARP was to determine whether lowering blood LDL cholesterol with simvastatin (20mg) plus ezetimibe (10mg) daily could safely reduce the risk of coronary heart disease, non-hemorrhagic stroke and the need for revascularization procedures in patients with chronic kidney disease (CKD). It also aimed to assess whether lowering LDL cholesterol reduced the rate of loss of renal function in people with CKD who had not commenced dialysis treatment.

Timeline

Start
2003-06
Primary completion
2010-08
Completion
2010-08

Outcome

Met primary endpoint

registry analysis (superiority or other test); Simvastatin Plus Ezetimibe vs Placebo; p = 0.0021; Risk Ratio (RR) 0.83 (95% CI 0.74 to 0.94); Log Rank NCT00125593 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ezetimibe Unknown 10 mg —
Subject Simvastatin Small molecule 20 mg —