Clinical Trials Directory

Trials / Completed

CompletedNCT00451100

Comparison of Rocuronium and Org 25969 With Cisatracurium and Neostigmine (19.4.310)(P05931)

Comparison of Rocuronium and Org25969 With Cisatracurium and Neostigmine When Neuromuscular Block is Reversed at Reappearance of T2

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
84 (actual)
Sponsor
Merck Sharp & Dohme LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to demonstrate in adult patients a faster recovery from a neuromuscular block with 2.0 mg/kg Org 25969 (sugammadex) after rocuronium as compared to 50 ug/kg neostigmine after cisatracurium when administered at reappearance of T2

Conditions

Interventions

TypeNameDescription
DRUGSugammadexSubjects received a bolus dose of 0.6 mg/kg rocuronium. After the last dose of rocuronium, at reappearance of T2, a dose of 2.0 mg/kg Org 25969 was to be administered
DRUGneostigmineSubjects received a bolus dose of 0.15 mg/kg cisatracurium. After the last dose of cisatracurium, at reappearance of T2, a dose of 50 ug/kg neostigmine was to be administered. In accordance to the labeling of neostigmine, a maximum of 5 mg neostigmine was to be administered

Timeline

Start date
2005-11-10
Primary completion
2006-05-22
Completion
2006-08-29
First posted
2007-03-23
Last updated
2019-11-15

Source: ClinicalTrials.gov record NCT00451100. Inclusion in this directory is not an endorsement.