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Prospective Multicenter Study to Assess the Safety and Efficacy of the Endomina® Triangulation Platform for Treating Patients Requiring Endoscopic Gastroplasty
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
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.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
Yes
Endo Tools Therapeutics S.A.
Gosselies, Wallonia, Belgium
Start Date
June 8, 2020
Primary Completion Date
March 31, 2023
Completion Date
March 31, 2026
Last Updated
January 10, 2023
1,000
ESTIMATED participants
Lead Sponsor
Endo Tools Therapeutics S.A.
NCT01143454
NCT07472881
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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