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Clinical Trials/NCT02350062
NCT02350062
Completed
Not Applicable

Comparison of Two Neuromuscular Monitors

University Hospital, Caen0 sites17 target enrollmentJanuary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neuromuscular Monitoring
Sponsor
University Hospital, Caen
Enrollment
17
Primary Endpoint
Time to recover T4/T1 > 90%
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Different neuromuscular monitors may be available in the same care structure. Two different monitors are available in the investigators' institution in the operative room and the recovery room. However, these two monitors have not been compared and may not be interchangeable. Starting the monitoring with one device and continuing with another device may be inaccurate and may lead to inadequate medical decisions. The investigators therefore conducted this observational study to compare the two devices available in our institution.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
November 2014
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing vascular surgery under general anesthesia and requiring neuromuscular blockade for intubation or surgery

Exclusion Criteria

  • Pregnancy or feeding
  • Any pathology or medication that may impair neuromuscular conduction or muscular response of the ulnar nerve stimulation
  • American Society of Anesthesiology \[4\] physical status
  • Allergy or contraindication of neuromuscular blocking agents

Outcomes

Primary Outcomes

Time to recover T4/T1 > 90%

Time Frame: Time between muscle relaxant injection and: intubation; recovery of 4 responses on the train of four (TOF); recovery of T4/T1 >40%; recovery of T4/T1>90% average 2 hours

After muscle relaxant injection, we measure the time needed for the muscular response to disappear and to completely recover during the operation (which takes in average 2 hours).

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