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NOT YET RECRUITING
NCT07894029
PHASE4

Effect of Neuromuscular Blocking Agent Use on Video Laryngeal Mask Airway Insertion

Sponsor: Hacettepe University

View on ClinicalTrials.gov

Summary

This study aims to investigate whether the administration of a neuromuscular blocking agent (rocuronium) improves the anatomical positioning of a third-generation video laryngeal mask airway (video LMA) in adult patients undergoing elective surgery under general anesthesia. A laryngeal mask airway is a device placed in the throat to maintain an open airway and support ventilation during general anesthesia. The third-generation video LMA incorporates a camera that allows the anesthesiologist to visualize the laryngeal structures and assess device positioning during insertion. Neuromuscular blocking agents reduce muscle tone and may facilitate airway device insertion. However, their potential benefits for the positioning and performance of video LMAs remain unclear. This is a prospective, randomized, controlled, parallel-group, outcome assessor-blinded clinical trial. Eligible patients will be randomly assigned to one of two groups. Both groups will receive propofol and remifentanil for anesthesia induction. The intervention group will additionally receive rocuronium (0.6 mg/kg), while the control group will receive no neuromuscular blocking agent. The primary outcome is the proportion of patients achieving optimal anatomical positioning of the video LMA, defined as a Brimacombe score of 4 on the integrated video image. Secondary outcomes include oropharyngeal leak pressure, insertion time, first-attempt insertion success, number of insertion attempts, ease of insertion, hemodynamic changes, ventilation parameters, airway-related complications, and postoperative adverse effects.

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

128

Start Date

2027-02-01

Completion Date

2028-02-01

Last Updated

2026-10-26

Healthy Volunteers

No

Interventions

DRUG

Rocuronium

Intravenous rocuronium 0.6 mg/kg administered during anesthesia induction, in addition to propofol and remifentanil, before video laryngeal mask airway placement.

DRUG

Standard Anesthesia Induction (Propofol and Remifentanil)

Both groups will receive intravenous propofol (2-2.5 mg/kg) and remifentanil (1 mcg/kg) during anesthesia induction before video laryngeal mask airway placement.

Locations (1)

Hacettepe University Faculty of Medicine Hospital

Ankara, Ankara, Turkey (Türkiye)