Randomised comparison of the Ambu® Laryngeal Mask with the Laryngeal Mask Airway UniqueTM during anaesthesia in spontaneously breathing adult patients

• Conditions: Airway maintenance during anaesthesia; Anaesthesiology - Other anaesthesiology; Respiratory -

• Registration Number: ACTRN12606000429550
• Lead Sponsor: Royal Melbourne Hospital - Department of Anaesthesia and Pain Management

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2006-10-04
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Adults who are undergoing general anaesthesia suitable for a LMA.

Exclusion Criteria

Recognised non suitability for supraglottic airway usage.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Airway leakage pressure[Measured just post device insertion]

Secondary Outcome Measures

Name	Time	Method
Time for insertion of device[As device is inserted];Adequacy of airway post insertion[Throughout the surgical procedure];Post operative sore throat[Immediately post surgery, 24 hrs post surgery]