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Trials / Completed

CompletedNCT03033979

Prolonged Laryngeal Mask Airway ProSealTM Use

Prolonged Use of the Laryngeal Mask Airway ProSealTM: a Report of Seven Cases Lasting 5-11 Hours

Status
Completed
Phase
Study type
Observational
Enrollment
7 (actual)
Sponsor
Schulthess Klinik · Academic / Other
Sex
All
Age
19 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The investigators conclude that use of the LMA ProSealTM for prolonged procedures is feasible. In principle, it should be safer and more effective than the LMA ClassicTM provided basic guidelines are followed.

Detailed description

There is controversy concerning use of the classic laryngeal mask airway (LMA ClassicTM) for prolonged procedures, particularly over 2 hours, as some clinicians consider it unsuitable for positive pressure ventilation (needed to counter the alleged progressive respiratory fatigue with time) and/or unsuitable for airway protection (needed to counter the alleged progressive increase in aspiration risk with time). The LMA ProSealTM is a laryngeal mask device with a modified cuff to facilitate ventilation and a drain tube to provide airway protection. In principle, the LMA ProSealTM should be more suitable than the LMA ClassicTM for prolonged procedures; however, there are only four reports and one case series.

Conditions

Timeline

Start date
2015-01-01
Primary completion
2015-12-31
Completion
2015-12-31
First posted
2017-01-27
Last updated
2017-01-27

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03033979. Inclusion in this directory is not an endorsement.

Prolonged Laryngeal Mask Airway ProSealTM Use (NCT03033979) · Clinical Trials Directory