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Clinical Trial Summary

To provide a research tool enabling physicians to monitor long term clinical outcomes for patients undergoing gastroesophageal reflux disease (GERD) treatment with EndoStim LES Stimulation System.


Clinical Trial Description

The EndoStim Patient Registry provides a framework for data collection on patients with GERD treated with the EndoStim LES Stimulation System. The primary objective is to provide a tool for participating physician investigators to collect and analyze outcomes data related to the use of the EndoStim LES Stimulation System.

This is a prospective, multi-center patient Registry. Sites may choose to also retrospectively enroll previously treated patients (after obtaining informed consent) and enter retrospective data into case report forms paper or on-line. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02441400
Study type Observational [Patient Registry]
Source EndoStim Inc.
Contact
Status Terminated
Phase
Start date May 2013
Completion date October 2019

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