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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of eupatilin on the prevention of gastroenteropathy in patients with NSAIDs and low dose steroid by comparing with rebamipide.


Clinical Trial Description

After being informed of the study and potential risks, all patients giving written informed consents will undergo a 1-week screening period to determine eligibility for study entry. During screening period, patients will undergo fecal calprotectin test, upper endoscopy and submit symptom diary. At week 0, subjects who meet the eligibility criteria will be randomized in a open labeled manner in 1:1 ratio to eupatilin (90mg twice daily-test group, 25 patients) or rebamipide (100mg three times daily-control group paients) for 8 weeks. At week 8, subjects undergo fecal calprotectin test, upper endoscopy and submit symptom diary. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04885751
Study type Interventional
Source Seoul National University Boramae Hospital
Contact
Status Not yet recruiting
Phase Phase 4
Start date June 1, 2021
Completion date January 31, 2022

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