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Respiration and The Airway With Supraglottic Airway Devices

NCT03384056 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2021-08-25

No results posted yet for this study

Summary

The investigators aim to compare the airway seal pressure( oropharyngeal leak pressure) of the Self Pressurized Airway Device with Blocker® with the ProsealTM Laryngeal Mask Airway (P-LMA)in anesthetized paralyzed adult female patients undergoing elective gynecological operations. The investigators aim at assessment of fitting of both devices against the glottic region that detected by the flexible fiberoptic bronchoscope( Pentex Corporation, Medical Division, Singapore)and assessment of any associated postoperative complications.

Hypothesis:

The investigators hypothesize that the self-pressurized air-Q with blocker has a greater seal pressure compared to Proseal, easier and faster in insertion with less morbidity and complications during and after its insertion.

Conditions

  • Laryngeal Masks Comparison

Interventions

DEVICE

Self Pressurized Airway Device with Blocker

used in adult low risk females undergoing elective gynecological operations

DEVICE

Proseal Laryngeal Mask Airway

used in adult low risk females undergoing elective gynecological operations.

Sponsors & Collaborators

  • Reham Ali Abdelhaleem Abdelrahman

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-02-01
Primary Completion
2019-10-01
Completion
2019-11-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03384056 on ClinicalTrials.gov