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
| Type | Name | Description |
|---|---|---|
| DEVICE | ProSeal LMA | ProSeal LMA vs Tracheal Tube |
| DEVICE | ProSeal LMA, Tracheal Tube | ProSeal 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.