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Clinical Trial Summary

The Revita DMR Post Market Pilot Clinical Registry is a post-market, prospective, observational, noninterventional clinical registry in patients with T2D in Germany undergoing the Revita Procedure with the CE marked Revita System (Fractyl Health, Lexington, MA, USA) in accordance with its intended purposes. Patient's participation in this study has no impact on his or her indication or opportunity to receive therapy. Patients are to be treated in compliance with the current Revita System's IFU of the CE marked Revita System as well as according to medical society guidelines and physician discretion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06256497
Study type Observational [Patient Registry]
Source Fractyl Health Inc.
Contact
Status Enrolling by invitation
Phase
Start date June 27, 2023
Completion date December 1, 2028

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