🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT07196696
Recruiting Not applicable

An in Vivo CT Imaging Study of GMA-Tulip, I-gel, and LMA Supreme (GLAM-II)

NCT07196696 · tracked via the Priya Life Science China tracker
Sponsor
Zhejiang Cancer Hospital
Phase
Not applicable
Started
2025-10-12
Last updated
2025-11-25

Condition(s) studied

Supraglottic Airway Device

Investigational drug(s) / intervention(s)

GMA-TulipI-gelLMA-Supreme insertion

GMA-Tulip: Under general anesthesia, GMA-Tulip laryngeal mask is inserted following standardized protocols. CT scanning and fiberoptic laryngoscopy are performed to assess insertion depth, anatomical alignment, and tissue compression.

I-gel: Under general anesthesia, I-gel laryngeal mask is inserted following standardized protocols. CT scanning and fiberoptic laryngoscopy are performed to assess insertion depth, anatomical alignment, and tissue compression.

LMA-Supreme insertion: Under general anesthesia, LMA Supreme laryngeal mask is inserted following standardized protocols. CT scanning and fiberoptic laryngoscopy are performed to assess insertion depth, anatomical alignment, and tissue compression.

Study summary

Laryngeal masks are core devices for supraglottic airway management, and the accuracy of their anatomical position directly impacts ventilation safety and the incidence of complications. Despite their wide clinical application, gaps remain in understanding their in vivo anatomical characteristics. This study aims to evaluate the in vivo anatomical features (e.g., insertion depth, anatomical alignment, tissue compression) of three laryngeal masks (LMA Supreme, I-gel, GMA-Tulip) using CT scanning in anesthetized patients undergoing CT interventional therapy, providing anatomical evidence for optimized laryngeal mask selection and complication prevention.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Aged 18-75 years, scheduled for CT interventional therapy; * Aged 18-75 years, scheduled for CT interventional therapy; * Body Mass Index (BMI) \<30 kg/m²; * Good communication and cooperation, with voluntary signing of the informed consent form. Exclusion Criteria: * Presence of head/neck or airway anatomical abnormalities (e.g., laryngeal cartilage malformation, Grade III tonsillar hypertrophy, tongue hypertrophy, cervical spine malformation) that may affect laryngeal mask insertion or CT imaging evaluation; * Current participation in other clinical studies.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Ethics Committee of Zhejiang Cancer Hospital Hangzhou Zhejiang Recruiting
Jiangling Wang Hangzhou Zhejiang Recruiting

More Zhejiang Cancer Hospital trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07196696 on ClinicalTrials.gov ↗ ← All trials in China