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Clinical Trials/ACTRN12608000240347
ACTRN12608000240347
Not yet recruiting
Phase 4

A randomised, single-blinded, controlled trial of the LMA® SupremeTM disposable laryngeal mask versus LMA® ClassicTM during anaesthesia in spontaneously breathing adult patients

Investigator Initiated (Daryl Williams)0 sites100 target enrollmentMay 8, 2008

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Supralaryngeal device in spontaneuosly breathing patients
Sponsor
Investigator Initiated (Daryl Williams)
Enrollment
100
Status
Not yet recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 8, 2008
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Investigator Initiated (Daryl Williams)

Eligibility Criteria

Inclusion Criteria

  • Adult undergoing spontaneous ventilation general anaesthesia in whom a supraglottic airway device would have been chosen for maintenance of airway patency by the Anaesthetist responsible for the individual patient.

Exclusion Criteria

  • Individuals undergoing general anaesthesia in whom it would not have been appropriate to insert a supraglottic airway device for airway patency as determined by the anaesthetist responsible for that patient will be excluded. Such patients include:· Patients with morbid obesity (Body Mass Index 35 kg/m2\)· Risk of aspiration· Limited interincisor distance (2\.5 cm)· Known difficult airway.Patients who are unable to communicate in English, because of a language barrier, cognitive deficit or intellectual disability will not be approached.

Outcomes

Primary Outcomes

Not specified

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