CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 201 enrolled
Drug / intervention
Protocol for rocuronium neuromuscular blockcombination
Likely dose
Not stated in 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/NCT03543826
NCT03543826Phase 4Completed

Best Practice With Rocuronium, Neostigmine, Sugammadex, and Subjective Monitoring.

University of Washington·interventional·Posted Jun 1, 2018·Updated Nov 9, 2022

In Brief

A Phase 4 clinical trial evaluating Protocol for rocuronium neuromuscular block for Muscle Weakness. Completed, enrolled 201 participants across 1 site.

Detailed Summary

This is an estimation study, prospectively evaluating the incidence of postoperative residual neuromuscular blockade (PRNB) when a best practice protocol is implemented for a cohort of abdominal surgery and orthopedic surgery patients. The protocol is developed within the constraint of subjective monitoring, quantitative monitoring is not used, and use of rocuronium for paralysis and either neostigmine or sugammadex for reversal. The primary outcome is the incidence of PRNB on arrival to the post-anesthesia care unit, defined as a train-of-four ration \<0.9.

Study Details

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

Timeline

Phase 4CompletedFinished
20192020202120222023202420252026
First PostedJun 1, 2018
Enrollment StartMay 21, 2018
Primary CompletionNov 26, 2018
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 8.1 years ago

Interventions

Protocol for rocuronium neuromuscular blockcombination

The protocol includes specified appropriate rocuronium dosing and a valid pre-reversal assessment of the adductor pollicis response guides optimal neostigmine vs. sugammadex reversal.