drugset / Trial / NCT00298831

Use of Sugammadex at the End of Case in Routine Anesthesia (MK-8616-023)

NCT00298831

Phase 3 Completed 224 enrolled Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of the study is to determine the time-course of recovery to a T4/T1 ratio of 0.9 within 4 minutes after 4.0 mg.kg\^-1 Sugammadex is administered at least 15 minutes after the last administration of rocuronium in a wide range of surgical procedures and anesthetic regimens (routine use). Safety evaluation is part of the study.

Timeline

Start
2005-10-27
Primary completion
2006-05-22
Completion
2006-05-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Sugammadex Other / unclassified 4 mg/kg Intravenous
Background Rocuronium Other / unclassified 0.15 mg/kg Intravenous

Indications

No indication recorded.