Comparison of Two Neuromuscular Transmission Monitors Based on Acceleromyography: TOF-Watch SX® and TOFScan® — TOFScan  

Neuromuscular Monitoring Clinical Trial

Official title: Comparison of Two Neuromuscular Transmission Monitors Based on Acceleromyography: TOF-Watch SX® and TOFScan®

Status Recruiting

Clinical Trial Summary

The purpose is to evaluate the reproducibility of neuromuscular monitoring data of recovery from neuromuscular blockade, obtained with TOFScan® and TOF-Watch SX®, in adult and pediatric population.

Secondary purposes are to evaluate the reproducibility of data obtained with 2 monitors for:

• the onset of clinical action of curare: suppression of the first response of train of four monitoring (T1) of 95% initial value

• the duration of clinical action of curare: recovery of the first response of train of four monitoring (T1) to 25% initial value

• recovery of first (T1), second (T2), third (T3) and fourth response (T4) of train of four monitoring, and recovery of T4/T1 to 40% and 60% initial value (T4/T1 0.4 and 0.6)

• complete recovery from curarisation, at T4/T1=90% and T4/T1=100%.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Curarisation
• Neuromuscular Monitoring

• NCT number: NCT02880787
• Study type: Interventional
• Source: Central Hospital, Nancy, France
• Contact: Thomas FUCHS-BUDER, Pr
• Email: t.fuchs-buder@chru-nancy.fr
• Status: Recruiting
• Phase: N/A
• Start date: November 2014
• Completion date: December 2016