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NCT02125838Completed

Laryngeal Mask Supreme During Laparoscopic Gynecologic Surgery

Application of Endotracheal Intubation and Laryngeal Mask Supreme Without Neuromuscular Blocker in Laparoscopic Gynecologic Surgery
Dokuz Eylul UniversityClinicalTrials.govdeviceDevice trial
Study focus
Disease/Condition
Anaesthesia
Drug/Device/Intervention
Laryngeal Mask Airway-Supreme
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Dokuz Eylul University
Location
Izmi̇r, Turkey
Timeline & enrollment
Phase
N/A
Start date
May 01, 2013
End date
Apr 01, 2015
Enrollment
108 participants
Primary outcome

Asses to Ventilation Parameters,Asses to Peak Pressure,Asses to Mean Pressure

Summary

Laryngeal mask (LM) use in gynecological laparoscopy, contrary to widespread opinion, does
 not increase the incidence of gastric aspiration, the failure of ventilation or the risk of
 pulmonary aspiration . LM is presented as an alternative to endo tracheal tube (ETT) in
 spontaneous or positive pressure ventilation (PPV) . LM has gained widespread popularity in
 England for gynecological laparoscopic procedures. In addition in many previous studies LM
 has been successfully shown to provide appropriate lung ventilation in laparoscopic surgical
 interventions .Miller et al. compared the use of ETT, LM-P laparoscopic gynecological
 interventions and identified advantages to LM use. The most important of these advantages was
 that, contrary to tracheal tube techniques for laparoscopic surgeries, use of supraglottic
 laryngeal devices or neuromuscular blocker agents (NBA) were not required during placement.
 Thus for laparoscopic surgeries, compared with the ETT technique, without the need for
 supraglottic laryngeal devices or muscular relaxants, it is easily placed and reduces the
 time spent in the operating room.
 
 Our aim; to compare the use of LM-S and ETT without neuromuscular agents for laparoscopic
 gynecological intervention with positive pressure ventilation from a surgical viewpoint and
 in terms of effect on ventilation parameters.
 
 Secondary aim, comparison of airway morbidity with endotracheal intubation and supraglottic.

ICD-10 classifications
Anaesthetic, unspecifiedOther and unspecified general anaestheticsOther complications of anaesthesiaLocal anaestheticsAnaesthesia of skin
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT02125838
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT02125838 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 108 participants.

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