RecruitingAccepts healthy volunteersPhase 1/Phase 2
Peppermint Oil for the Treatment of Interstitial Cystitis / Bladder Pain Syndrome
University of Louisville · with Integrative Therapeutics, Inc. · NCT04845217
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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1, Phase 2
- Target enrollment
- 100
- US sites recruiting
- 1
- Study start
- September 15, 2021
- Record last updated
- August 22, 2022
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to assess the use of peppermint oil as a treatment for Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS).
Being studied: Peppermint oil; Coconut Oil
Conditions: Interstitial Cystitis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full 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
Recruiting US locations
Springs Medical Center
Louisville, KY 40205
Site contact: Sean Francis, MD
Study contacts (from the official record)
- Jenna Warehime, DO · 502-588-7660 · pepperminttrial@gmail.com
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