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Clinical Trial Summary

This registry is designed to further assess on a larger scale safety and efficacy of the endomina® device and tissue apposition accessories (TAPES) when used in the frame of "real life" routine clinical practice


Clinical Trial Description

This is a single arm prospective, multi-center international, open-label, non-interventional, , post-market study. This registry is designed to further assess on a larger scale safety and efficacy of the endomina® and TAPES devices. Patients in need of endoscopic gastroplasty will be enrolled and followed-up for 36 months following hospital routine practice. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05677464
Study type Observational [Patient Registry]
Source Endo Tools Therapeutics S.A.
Contact Mrs Leclercq
Phone 003271495517
Email pretti@endotools.be
Status Recruiting
Phase
Start date June 8, 2020
Completion date March 31, 2026

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