What this study is
The goal of this clinical trial is to study the effect of peppermint oil in in children with bladder and bowel dysfunction.
The main question it aims to answer is: Does peppermint oil improve symptoms of bladder and bowel dysfunction among children?
Participants will:
- Be provided peppermint oil capsules to be taken 3 times daily for 8 weeks.
- At baseline and at a follow-up visit (8 weeks later), participants will be asked to complete the Vancouver Nonneurogenic Lower Urinary Tract Dysfunction/Dysfunctional Elimination Syndrome Questionnaire.
Researchers will compare baseline and follow-up questionnaire data for each participant to determine if there is improvement in symptoms of bladder and bowel dysfunction.
What's being tested
- Peppermint Oil
Intervention · DIETARY SUPPLEMENT
Participants weighing more than 40 kg will receive 2 peppermint oil capsules 3 times a day. Smaller children who weigh between 30 kg and 40 kg will receive 1 capsule of peppermint oil 3 times a day. All subjects will receive 8 weeks of treatment.
Study details
- Official title
- Peppermint Oil as an Alternative Treatment for Children With Bladder and Bowel Dysfunction: A Prospective Study
- Sponsor
- Children's Hospital of Orange County
- Conditions
- Bladder and Bowel Dysfunction
- Enrolling
- 30 people
- Starts
- 2022-11-01
- Est. completion
- 2026-12-31
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 8 Years – 17 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Children aged 8-17 years and weighing 30kg or more with non-neurogenic bladder and bowel dysfunction who have failed behavioral therapy. Behavioral therapy, or also termed standard urotherapy, is defined as encompassing the following components [15]: Information and demystification; instruction on avoidance of holding maneuvers, regular bowel habits, proper voiding posture; lifestyle advice encompassing balanced fluid intake and diet, diminished caffeine, regular bladder and bowel emptying patterns; registration of symptoms and voiding habits with bladder diaries or frequency-volume charts; support and encouragement via regular follow up with caregiver. Failure of behavioral therapy is defined as no symptomatology improvement after adherence to behavioral therapy after 6 weeks.
- Participants must be able to swallow pills
You can't join if
- Patients with neurogenic bladder, tethered cord, Society of Fetal Urology grade 3-4 hydronephrosis, vesicoureteral reflux, learning disabilities, or those who have undergone surgical therapy for bladder and bowel dysfunction will be excluded.
- Patients on medical therapy with oxybutynin within the last 30 days.
- Patients with hiatal hernia, severe gastrointestinal reflux or gallbladder disorders or on medications for these conditions will be excluded.
- Patient weighing less than 30 kg.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openChildren's Hospital, Orange County
Orange, California, United States
Study team
Sponsor
Children's Hospital of Orange County
Study ID 2206102
Principal investigator
Heidi A. Stephany, MD
Children's Hospital, Orange County
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.