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Clinical Trial Summary

This is a post-market, multi-center, double-blind, placebo-controlled, randomized, cross-over study with GERDOff Plus added on top of the current PPI treatment in patients with GERD. The aim of the study is to evaluate the performance of GERDOff Plus, a class III medical device, consisting in a hyaluronic acid, chondroitin sulphate and magnesium trisilicate, in addition to the PPIs, in patients with GERD not fully satisfied with their current treatment with PPIs. Patients will receive either GERDOff Plus or placebo q.i.d. for 21 days followed by a wash-out period of 3 weeks. After the wash-out period, the patients will receive either placebo or GERDOff Plus respectively


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04202692
Study type Interventional
Source SOFAR S.p.A.
Contact
Status Completed
Phase N/A
Start date November 5, 2019
Completion date November 23, 2022

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