drugset / Trial / NCT00244504

Moxonidine in Patients Undergoing Vascular Surgery

NCT00244504

Phase 3 Terminated 141 enrolled University Hospital, Basel, Switzerland
RandomizedParallel-groupQuadruple-blindPrevention

Summary

Investigating the perioperative effect of moxonidine. In a randomized double-blind fashion, patients undergoing vascular surgery will receive moxonidine 0.2 mg or placebo from the day before surgery until day 4 after surgery. Holter-EKG for 48 h, starting just before surgery. Repeated 12-lead EKG, measurements of Troponin I and BNP, clinical visitations, follow-up interviews at 6 and 12 months

Timeline

Start
2002-11
Primary completion
2006-03
Completion
2006-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Moxonidine Small molecule 0.2 mg Oral

Indications