- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01086176
The Impact of Post-tetanic Count on Subsequent Train-of-four During Recovery From Rocuronium
April 26, 2010 updated by: Maisonneuve-Rosemont Hospital
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 Overview
Status
Completed
Study Type
Observational
Enrollment (Anticipated)
22
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Quebec
-
Montréal, Quebec, Canada, H1T 2M4
- Hopital Maisonneuve-Rosemont
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Poeple having general anesthesia at HMR
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patient-control
|
on one side, we do a post-tetanic count, on the other side we don't, after, we do train-of-four on both sides and check the difference
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
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 Outcome Measures
Outcome Measure |
---|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2010
Primary Completion (ACTUAL)
April 1, 2010
Study Completion (ACTUAL)
April 1, 2010
Study Registration Dates
First Submitted
March 10, 2010
First Submitted That Met QC Criteria
March 11, 2010
First Posted (ESTIMATE)
March 12, 2010
Study Record Updates
Last Update Posted (ESTIMATE)
April 27, 2010
Last Update Submitted That Met QC Criteria
April 26, 2010
Last Verified
March 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- MaisonneuveRH-09092
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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