Clinical Trials Directory

Trials / Completed

CompletedNCT00402870

Postoperative Analgesic Requirements for the ProSeal Laryngeal Mask Airway Versus the Tracheal Tube in Females Undergoing Gynecological Laparoscopic Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Medical University Innsbruck · Academic / Other
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

The ProSeal laryngeal mask airway is a relatively new airway device with a modified cuff to increase the seal and a drain tube to provide a channel for regurgitated fluid, prevention of gastric insufflation and insertion of a gastric tube. In the following randomized prospective double-blind trial, we test the hypothesis that the postoperative analgesic requirements is higher for the ProSeal laryngeal mask airway than the tracheal tube.

Conditions

Interventions

TypeNameDescription
DEVICEProSeal LMAProSeal LMA vs Tracheal Tube
DEVICEProSeal LMA, Tracheal TubeProSeal LMA vs Tracheal Tube

Timeline

Start date
2007-08-01
Completion
2007-09-01
First posted
2006-11-22
Last updated
2007-12-04

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT00402870. Inclusion in this directory is not an endorsement.

Postoperative Analgesic Requirements for the ProSeal Laryngeal Mask Airway Versus the Tracheal Tube in Females Undergoin (NCT00402870) · Clinical Trials Directory