Ventilation Safety in Beach Chair Shoulder Surgery: SafeLM Versus I-gel
NCT: NCT07501468 · NOT_YET_RECRUITING
Brief Summary
This study aims to compare the performance of SafeLM™ video laryngeal mask airway and i-gel® supraglottic airway device in patients undergoing shoulder surgery in the beach chair position under general anesthesia. The primary objective is to evaluate oropharyngeal leak pressure (OLP) within the first 10 minutes after transition to the beach chair position. Secondary objectives include assessment of ventilation safety, need for airway interventions, and postoperative airway-related complications. This prospective randomized study will provide data on the effectiveness and safety of a video-guided supraglottic airway device compared to a conventional device in a clinically challenging position.
Frequently Asked Questions
What is Ventilation Safety in Beach Chair Shoulder Surgery: SafeLM Versus I-gel?
Ventilation Safety in Beach Chair Shoulder Surgery: SafeLM Versus I-gel is a clinical trial registered under NCT07501468. Current status: NOT_YET_RECRUITING.
What is the status of NCT07501468?
The current status of NCT07501468 (Ventilation Safety in Beach Chair Shoulder Surgery: SafeLM Versus I-gel) is: NOT_YET_RECRUITING.
When did Ventilation Safety in Beach Chair Shoulder Surgery: SafeLM Versus I-gel start?
Ventilation Safety in Beach Chair Shoulder Surgery: SafeLM Versus I-gel started on 2026-04-15.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.