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.
Investigators
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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