This study is currently not recruiting participants.

A Worldwide Post-Market Surveillance Registry to assess the Medigus Ultrasonic Surgical Endostapler (MUSE) System for the treatment of GERD

  • STATUS
    Not Recruiting
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Updated on 19 February 2024

Summary

The purpose of this study is to collect observational, post-market surveillance data such as: baseline demographics, follow up measurements, device performance, user experience, user experience, and safety and effectiveness of the commercially available MUSE system for a minimum of 3 year follow up on a large number of subjects in a worldwide setting.

Description

The purpose of this study is to collect observational, post-market surveillance data such as: baseline demographics, follow up measurements, device performance, user experience, user experience, and safety and effectiveness of the commercially available MUSE system for a minimum of 3 year follow up on a large number of subjects in a worldwide setting.

Details
Condition GERD
Age 100years or below
Clinical Study IdentifierTX5122
Last Modified on19 February 2024

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