drugset / Trial / NCT00859183

Oral Sirolimus for In-Stent Restenosis

NCT00859183

Phase 4 Completed 300 enrolled German Heart Center Munich
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Despite recent advances in interventional cardiology including the success of drug-eluting stents in de-novo coronary lesions, the treatment of in-stent restenosis remains a challenging clinical issue. Given the efficacy of the systemic sirolimus administration to prevent neointimal hyperplasia in animal models and to halt and even reverse the progression of allograft vasculopathy, the aim of the present double-blind, placebo-controlled study was to evaluate the efficacy of a 10-day oral sirolimus treatment with two different loading regimens for the prevention of recurrent restenosis in patients with in-stent restenosis.

Timeline

Start
2001-10
Primary completion
2004-02
Completion
2004-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Sirolimus Small molecule 2 mg Oral

Indications