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Clinical Trial Summary

Hernia Reduction Prior to Scheduled TIF Completion using EsophyX ZR transoral device


Clinical Trial Description

Evaluation of the relative merits, safety and effectiveness of the EsophyX ZR transoral device in performing the standardized TIF 2.0 procedure preceded by laparoscopic Hiatal Hernia repair in PPI-prescribed patients with persistent "troublesome symptoms" per the Montreal consensus definition ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03280121
Study type Interventional
Source EndoGastric Solutions
Contact
Status Terminated
Phase N/A
Start date October 5, 2018
Completion date October 26, 2020

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