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NCT02127632Completed

Comparison of Laryngeal Mask Airway Supreme and Endotracheal Tube In Patients Undergoing Gynecological Laparoscopy Surgery

Dokuz Eylul UniversityClinicalTrials.govdeviceDevice trial
Verified
Study focus
Disease/Condition
Anaesthesia
Drug/Device/Intervention
Endotracheal Tube
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Dokuz Eylul University
Location
Izmi̇r, Turkey
Timeline & enrollment
Phase
N/A
Start date
Apr 01, 2012
End date
May 01, 2013
Enrollment
100 participants
Primary outcome

Mean Airway Pressures

Summary

Endotracheal Tube (ETT) is still preferred for laparoscopic surgeries because of the fear of
 pulmonary aspiration and inadequate ventilation. Laryngeal mask Supreme (LM-S) is a single
 use device and the presence of a drain tube allows to separate the gastrointestinal and
 respiratory tracts. We planned to compare ventilation parameters and gastric distension
 scores of with LM-S vs ETT during laparoscopic gynecological surgery.

ICD-10 classifications
Anaesthetic, unspecifiedOther and unspecified general anaestheticsOther complications of anaesthesiaLocal anaestheticsAnaesthesia of skin
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT02127632
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT02127632 through Pure Global AI's free database. This phase not specified trial is sponsored by Dokuz Eylul University and is currently Completed. The study focuses on Anaesthesia. Target enrollment is 100 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.