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Clinical Trial Summary

The purpose of this study is to assess the use of peppermint oil as a treatment for Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS).


Clinical Trial Description

After being informed about the study and potential risks, all participants will complete validated IC/BPS symptom questionnaires for baseline screening. Once participants meet eligibility requirements and give written informed consent they will be randomized in a 1:1 ratio to peppermint oil (200mg TID) or placebo (also TID). Participants will complete validated IC/BPS questionnaires and follow up surveys over 8 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04845217
Study type Interventional
Source University of Louisville
Contact Jenna Warehime, DO
Phone 502-588-7660
Email pepperminttrial@gmail.com
Status Recruiting
Phase Phase 1/Phase 2
Start date September 15, 2021
Completion date December 2023

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