CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 100 enrolled
Drug / intervention
Sugammadex administrationdrug
Likely dose
Sugammadex administration 50 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05246397
NCT05246397Phase 4Completed

Sugammadex Titration for Reversal of Rocuronium or Vecuronium in Cardiac Surgery Patients

University of Washington·interventional·Posted Feb 18, 2022·Updated Mar 21, 2024

In Brief

A Phase 4 clinical trial evaluating Sugammadex administration for Coronary Artery Disease and 3 related conditions. Completed, enrolled 100 participants across 1 site.

Detailed Summary

Sugammadex is frequently used to reverse the effects of neuromuscular blocking drugs. The recommended doses are 2 mg/kg or 4 mg/kg depending upon the depth of neuromuscular blockade. Clinical studies and experience have suggested that smaller doses may be effective. The purpose of this observational study is to determine the minimal effective dose of sugammadex by administering 50 mg every 5 minutes until the train-of-four ratio is 0.9 in a cohort of cardiac surgery patients, and to determine the duration of action by measuring the train-of-four every hour for up to 6 hours following reversal.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
20222023202420252026
First PostedFeb 18, 2022
Enrollment StartFeb 1, 2022
Primary CompletionNov 10, 2022
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 4.4 years ago

Interventions

Sugammadex administrationdrug

Sugammadex will be given in 50 mg increments every five minutes for reversal of neuromuscular blockade until reaching a train-of-four ratio of 0.9