drugset / Trial / NCT00420680

Safety and Efficacy Evaluation of Sugammadex in Cardiac Patients (19.4.309)(P05934)

NCT00420680

Phase 3 Completed 120 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety of 2.0 mg/kg and 4.0 mg/kg sugammadex given as a reversal agent at reappearance of T2 after 0.6 mg/kg rocuronium in cardiac patients

Timeline

Start
2005-11-07
Primary completion
2006-08-01
Completion
2006-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sugammadex Other / unclassified 2 mg/kg
Subject Sugammadex Other / unclassified 4 mg/kg

Indications

No indication recorded.