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Clinical Trials/NCT00668278
NCT00668278
Completed
Not Applicable

I-Gel Versus Disposable Laryngeal Mask Airway for General Anesthesia With Controlled Ventilation

Northern Health and Social Care Trust0 sites200 target enrollmentFebruary 2008
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ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Northern Health and Social Care Trust
Enrollment
200
Primary Endpoint
Sealing pressure and peak airway pressure.
Status
Completed
Last Updated
17 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

Randomized controlled trial comparing performance of the I-gel and disposable Laryngeal Mask Airways under controlled ventilation. 200 patients, 100 in each arm. Measurement of peak airway and sealing pressures. Postoperative questionnaires at 1 and 24hrs.

Hypothesis

There is no difference between the performance* of the I-gel and disposable laryngeal mask airways for controlled ventilation under general anesthesia.

*as defined by peak airway pressure and sealing pressures.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
January 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Males and females.
  • •Age 18-89 inclusive.
  • •ASA grade 1-
  • •Elective surgery

Exclusion Criteria

  • •Emergency surgery.
  • •Surgery within the peritoneum.
  • •Surgery requiring prone or steep head-down positioning.
  • •Patients at increased risk of aspiration

Outcomes

Primary Outcomes

Sealing pressure and peak airway pressure.

Time Frame: Under anaesthesia.

Secondary Outcomes

  • Postoperative patient symptoms(1hr and 24hrs postoperatively)

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