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Clinical Trial Summary

The purpose of the study is evaluate the safety and efficacy of L-glutamine as a treatment for patients with diverticulosis.


Clinical Trial Description

After being informed about the study and potential risks, all patients giving written informed consent will undergo a 4 weeks screening period to determine eligibility for study entry. At Week 0, patients who meet eligibility requirements will be given L-glutamine (15 grams, twice daily) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05106101
Study type Interventional
Source Emmaus Medical, Inc.
Contact
Status Completed
Phase Phase 1
Start date July 19, 2019
Completion date December 30, 2022

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