Video Laryngeal Mask vs. Endotracheal Tube in Septoplasty

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorSamsun University

About this trial

This randomized controlled trial compares a video laryngeal mask airway (VLMA) and an endotracheal tube (ETT) in adult patients undergoing elective septoplasty. The primary objective is to see which device more effectively prevents surgical blood contamination in the glottic and subglottic regions. The study also assesses perioperative hemodynamic stability, ventilation parameters, and postoperative recovery factors such as sore throat, hoarseness, and overall patient comfort. The findings aim to help determine the optimal airway device choice for nasal surgeries.

Eligibility criteria

Qualifiers

ASA I-II classification patients

Patients aged 18-65 years undergoing elective septoplasty

Disqualifiers

ASA III-IV classification patients

Patients with anticipated difficult airway

Patients under 18 years of age

History of gastroesophageal reflux disease (GERD) or hiatal hernia

Trial design

Treatments tested in this trial

  • Video Laryngeal Mask Airway (VLMA)
  • Endotracheal Tube (ETT)

Treatment groups

64 Participants
are divided into 2 treatment groups

Sponsors and collaborators