← Eichor
Study identifier: NCT06950957 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Video Laryngeal Mask vs. Endotracheal Tube in Septoplasty

Condition: Airway Complication of Anesthesia · Anesthesia Intubation Complication · Septoplasty  ·  Sponsor: Samsun University

PhaseN/A
Planned participants64
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Hatice Selcuk KUSDERCI, M.D.  ·  +905052159896  ·  drkusderci@hotmail.com

Ahmet Ozan Aydin, M.D.  ·  +905438956146  ·  ahmetozanaydin@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Samsun University, Samsun Training and Research HospitalSamsun, Ilkadim, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06950957