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Clinical Trials/NCT01086176
NCT01086176CompletedNot Applicable

The Impact of Post-tetanic Count on Subsequent Train-of-four During Recovery From Rocuronium

Maisonneuve-Rosemont Hospital1 site in 1 country22 target enrollmentStarted: March 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
22
Locations
1
Primary Endpoint
The difference at 30 minutes after the post-tetanic count between the TOF% in both arms, we expect a difference of more than 10%

Study Overview

Brief Summary

The purpose of this study is to see how long does the effect of a post-tetanic facilitation last on subsequent train-of-four. The investigators hypothesis is that the effect last at least 30 minutes.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patient having general anesthesia in dorsal decubitus with both arm available for at least an hour and a half

Exclusion Criteria

  • Age >75 or <18
  • Neuromuscular disease
  • difficult laryngoscopy predicted
  • Allergy to rocuronium
  • Malignant hyperthermia
  • Full stomach
  • Drugs the influence neuromuscular blockers
  • Decision of the clinician to exclude his patient

Outcomes

Primary Outcomes

The difference at 30 minutes after the post-tetanic count between the TOF% in both arms, we expect a difference of more than 10%

Secondary Outcomes

  • The difference at 30 minutes after the post-tetanic count on the T1% (of the calibrated T1) in both arms, we expect a difference of more than 10%
  • The difference of the slope of recuperation on TOF and T1% after a post-tetanic count vs the control arm that had no tetanic stimulation

Investigators

Sponsor Class
Other

Study Sites (1)

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