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Peppermint Oil for the Treatment of Interstitial Cystitis / Bladder Pain Syndrome
RecruitingPhase 1/2Healthy volunteers welcome
Efficacy of Peppermint Oil in a Randomized, Single-Blind, Placebo Controlled Trial in Women With Interstitial Cystitis/Bladder Pain Syndrome
Who can join
Ages 18 to 65 · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Women ages 18-65 years old * Diagnosed with IC/BPS for at least one month prior to study enrollment Exclusion Criteria: * Culture proven urinary tract infection within 1 month of randomization * Gross hematuria * Currently pregnant or breastfeeding * Unable to speak and read English * History of allergic reaction to peppermint, coconut or enteric coating * History of malabsorption syndrome * History of gastroparesis * History of gastric bypass surgery * History of gastrointestinal, genitourinary or pelvic cancer in the last 5 years * History of insulin dependent diabetes * History of active urinary stone disease
About the study
The purpose of this study is to assess the use of peppermint oil as a treatment for Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS).
What is being tested
- Peppermint oil (drug)
- Coconut Oil (drug)
Sponsor: University of Louisville · Participants: 100 · Started: Sep 15, 2021
Contact the study team
- Jenna Warehime, DO · Phone: 502-588-7660
Official record on ClinicalTrials.gov — NCT04845217
Locations in the U.S.
| Kentucky | Springs Medical Center, Louisville |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.