Skip to main content
Clinical Trials/NCT00338559
NCT00338559CompletedNot Applicable

Does Using Laryngeal Mask Airway (LMA) Instead of an Endotracheal Tube (ET Tube) Affect the Incidence of Postoperative Vomiting in Children Undergoing Strabismus Correction? - An Observational Study

The University of Texas Health Science Center, Houston1 site in 1 country71 target enrollmentStarted: May 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
71
Locations
1
Primary Endpoint
Numbers of the patients that will develop postoperative vomiting in children undergoing strabismus correction

Study Overview

Brief Summary

The effect of airway management on vomiting after strabismus surgery is unknown. The purpose of this study is to find out whether the use of different airway devices, such as LMA, which is a special mask placed in the throat or Endotracheal tube (ET tube), which is a soft tube placed in the wind pipe, affects the incidence of vomiting after surgery. Two hundred six children between the ages of 2 and 12 years are expected to take part in this study.

Detailed Description

The child will be checked by the study doctor to determine if he/she qualifies to be part of the study. The study doctor may not want the child to take part in this study if he/she is currently in another research study; or if the child has been in any other research study within the last 30 days, or if the child is extremely obese, or has reflux or another GI problem.

If the child qualifies for the study, he/she will receive routine general anesthesia. For airway management, the child will have either a LMA or ET tube. The child has an equal chance of receiving either one of these airways devices, much like the coin flip.

After surgery, the child will be transferred to the recovery room (PACU). If the child vomits in PACU, he/she will receive rescue medication, which can be repeated if the need arises.

A research coordinator will call the parents the following day to find out whether the child vomited after leaving the hospital, in the car or at home, for any complications and receiving any medications.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
1 Year to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with Elective Uni- or Bilateral Strabismus repair

Exclusion Criteria

  • History of Prematurity
  • History of Reflux
  • History of Neurological Disease
  • Difficult Airway

Outcomes

Primary Outcomes

Numbers of the patients that will develop postoperative vomiting in children undergoing strabismus correction

Time Frame: 2 days

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Samia Khalil

Professor - Anesthesiology

The University of Texas Health Science Center, Houston

Study Sites (1)

Loading locations...

Similar Trials