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Comparison of the TOFScan and the WiTOF During Recovery of Neuromuscular Function

NCT05231525 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2022-12-01

No results posted yet for this study

Summary

The purpose of this study is to compare two neuromuscular blockade monitors on recovery from an ATRACURIUM intra veinous injection for surgery. The TOFscan, a wired connected monitors and the WiTOF, a wireless connected monitor.

Conditions

  • Neuromuscular Residual Curarization

Interventions

DEVICE

WiTOF

Data collection on the WiTOF monitor

DEVICE

TOFscan

Data collection on the TOFscan monitor

Sponsors & Collaborators

  • Poitiers University Hospital

    lead OTHER

Principal Investigators

  • Matthieu BOISSON · CHU de Poitiers FRANCE

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-09
Primary Completion
2022-06-20
Completion
2022-09-20

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05231525 on ClinicalTrials.gov