Comparing the ProSeal laryngeal mask airway with standard endotracheal tube in gynaecological laparoscopy

Phase 4

Completed

• Conditions: Post operative pain; Anaesthesiology - Anaesthetics

• Registration Number: ACTRN12611000930987
• Lead Sponsor: Dr James Griffiths

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-08-30
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 120

Inclusion Criteria

Adult female patients undergoing relaxant general anaesthesia for intermediate-duration gynaecological laparoscopy

Exclusion Criteria

Anticipated surgical duration less than 30 minutes or greater than 120 minutes
Contraindications to the use of a LMA in laparoscopic surgery - obesity, symptoms of gastroesophageal reflux, known or anticipated difficult airway
Contraindications to any study drug (including morphine and parecoxib)

Study & Design

• Study Type: Interventional
• Study Design: Not specified