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Summative Evaluation to Validate the LEAFix Device With Users — LEAFIXUser  

Anesthesia Clinical Trial

Official title:
Summative Evaluation to Validate That the Laryngeal, Endo-tracheal, Airway Fixator (LEAFix) Can be Used Safely and Effectively by Intended Users to Secure Airway Devices

Clinical Trial Summary

The Laryngeal Endo-tracheal Airway Fixator(LEAFix) is a single use product designed to secure airway devices to patients during anaesthesia, with better infection control management and interaction with the patients skin. This study investigates the users of the LEAFix device interacting with the LEAFix device, its packaging and a simulated patient through different scenarios of securing an airway device. The aim is to understand the risks associated with the use of the device for CE marking purposes. This study is funded by Innovel Ltd. the manufacturer of the device.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05255432
Study type Observational
Source Liverpool University Hospitals NHS Foundation Trust
Contact Richard Ramsaran, MBChB
Phone 07709674876
Email richard.ramsaran@liverpoolft.nhs.uk
Status Not yet recruiting
Phase
Start date June 2022
Completion date September 2022
View Details
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