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CompletedNCT01479764

Study of Sugammadex Versus Usual Care on Incidence of Residual Blockade at Post Anesthesia Care Unit Admission (P07981)

Effect of Sugammadex Compared With Usual Care for Reversal of Neuromuscular Blockade Induced by Rocuronium on Incidence of Residual Blockade at PACU Entry

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

Summary

This study will compare the incidence of residual neuromuscular blockade in participants who undergo reversal of neuromuscular blockade with sugammadex compared to those who undergo reversal of neuromuscular blockade with usual care (neostigmine/glycopyrrolate).

Conditions

Interventions

TypeNameDescription
DRUGSugammadexsugammadex, intravenous (IV) bolus, 2 or 4 mg/kg depending on level of neuromuscular recovery
DRUGNeostigmineneostigmine, per usual practice
DRUGGlycopyrrolateglycopyrrolate per usual practice

Timeline

Start date
2011-12-02
Primary completion
2012-10-26
Completion
2012-11-05
First posted
2011-11-24
Last updated
2017-06-06
Results posted
2013-12-31

Source: ClinicalTrials.gov record NCT01479764. Inclusion in this directory is not an endorsement.

Study of Sugammadex Versus Usual Care on Incidence of Residual Blockade at Post Anesthesia Care Unit Admission (P07981) (NCT01479764) · Clinical Trials Directory