Peppermint Oil for the Treatment of Irritable Bowel Syndrome or Functional Abdominal Pain in Children: the MINT Study

Irritable Bowel Syndrome Clinical Trial

— MINT  

Official title:

Peppermint Oil for the Treatment of Irritable Bowel Syndrome or Functional Abdominal Pain in Children: the MINT Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05799053
• Other study ID #: NL78304.100.21
• Status: Recruiting
• Phase: Phase 3
• Start date: May 12, 2022
• Est. completion date: December 31, 2024

Study information

• Verified date: April 2024
• Source: St. Antonius Hospital
• Contact: Koen Vermeijden, MD
• Phone: (+31) 020-566 2906
• Email: k.vermeijden[@]antoniusziekenhuis.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Peppermint oil has shown to be effective in the treatment of Irritable Bowel Syndrome (IBS) symptoms in adults. Few studies of low quality are performed in an paediatric setting. Therefore, the investigators will conduct a multicenter randomized, placebo controlled trial to investigate the effects of an eight-week peppermint oil treatment in paediatric IBS or Functional Abdominal Pain - Not otherwise specified (FAP-NOS) patients.

Description:

The objective of the MINT study is to investigate the effectiveness of peppermint oil capsules compared to placebo capsules in reducing abdominal pain intensity in children with IBS or FAP-NOS. In addition, we evaluate the effect of peppermint oil capsules compared to placebo capsules on other disease-related outcome measures such as anxiety & depression, quality of life, absenteeism from school, and healthcare costs. The second aim is to explore the effectiveness of regular mints in reducing abdominal pain intensity compared to peppermint oil capsules and placebo capsules and the effect of mints on secondary outcome parameters.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 240
• Est. completion date: December 31, 2024
• Est. primary completion date: November 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 8 Years to 17 Years

Eligibility

Inclusion Criteria:

• Children aged between 8 years and 18 years

• Diagnosis of IBS or FAP-NOS according to the Rome IV criteria. According to these criteria, organic disorders will be ruled out after routine laboratory testing initiated by their general practitioner or treating physician as part of standard of care. In patients without alarm symptoms only celiac screening (anti-transglutaminase antibodies and IgA), and faecal calprotectin are necessary.37 In patients with diarrhea faecal testing for Giardia Lambliae will be added. If alarm symptoms are present, further diagnostic testing (like a full blood count, CRP, liver tests or an ultrasound) to rule out an organic disorder, is left to the discretion of the treating physician.

• An average daily pain rate of = 3 of 10 on the Wong Baker Faces Pain Scale (This is a validated pain scale to measure pain intensity).

Informed Consent by both parents and by children aged = 12 years. No informed consent from parents is necessary for children >16 years.

Exclusion Criteria:

• Current treatment by another health care professional for abdominal symptoms

• Previous use of peppermint oil for these abdominal complaints

• Known hypersensitivity to mints or peppermint oil

• Gastrointestinal blood loss

• Recurrent or unexplained fevers

• Decreased growth velocity

• History of previous abdominal surgeries in the past 3 months

• Significant chronic health condition requiring specialty care (e.g., lithiasis, ureteropelvic junction obstruction, sickle cell, cerebral palsy, hepatic, hematopoietic, renal, endocrine, or metabolic diseases) that could potentially impact the child's ability to participate or confound the results of the study

• Known concomitant organic gastrointestinal disease

• Current use of drugs which influence gastrointestinal motility, such as erythromycin, azithromycin, butyl scopolamine, domperidone, mebeverine and Iberogast. If laxatives are being used (in patients with IBS-C) they can continue using them during the study.

• Current use of proton-pump inhibitors

• Insufficient knowledge of the Dutch language

• Pregnancy or current lactation. Women with childbearing potential must have a negative urine pregnancy test within 7 days prior to first dose of study treatment

Related Conditions & MeSH terms

• Abdominal Pain
• Adolescent
• Adverse Drug Event
• Child
• Drug-Related Side Effects and Adverse Reactions
• Functional Abdominal Pain Syndrome
• Irritable Bowel Syndrome
• Syndrome
• Therapeutics

Intervention

Drug:
• Small intestinal release peppermint oil
Tempocol®, a gastric acid resistant (enteric-coated) capsule containing 182mg of Menthae Piperitae Aetheroleum (peppermint oil), is currently registered as an over the counter prescription drug on the Dutch market for treatment of abdominal pain, discomfort or flatulence.
• Peppermint sweets
Wilhelmina® peppermints contain 9.2 mg of Menthae Piperitae Aetheroleum (peppermint oil), and 18.4 Kcal per mint and are to be taken orally.
• Placebo
Capsule containing microcrystalline cellulose

Locations

Country	Name	City	State
Netherlands	De KinderKliniek	Almere	Flevoland
Netherlands	Amsterdam UMC	Amsterdam	Noord-Holland
Netherlands	Amphia Hospital	Breda	Noord-Brabant

Sponsors (1)

Lead Sponsor	Collaborator
St. Antonius Hospital

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Abdominal pain intensity response rate after 8 weeks of treatment	The proportion of patients with = 30% reduction of their abdominal pain intensity after 8 weeks of therapy compared to baseline. This will be assessed by a smartphone diary app, on which patients record daily at the end of the day the intensity of their abdominal pain during a period of 7 consecutive days using a 10 point Likert scale/Wong-Baker faces scale. A score of 0 correlates with no pain and a score of 10 correlates with the worst imaginable pain. The intensity scores of 7 days will be summed up.	8 weeks
Secondary	Change in pain duration	Abdominal pain duration will be scored in minutes of abdominal pain per day during 7 consecutive days after 8 weeks of therapy compared to baseline	4 weeks, 8 weeks, 12 weeks
Secondary	Change in pain frequency	Abdominal pain frequency will be scored as the average amount of days with pain during 7 consecutive days after 8 weeks of therapy compared to baseline	4 weeks, 8 weeks, 12 weeks
Secondary	Change in abdominal pain intensity	Abdominal pain intensity will be scored using a 10-point Wong-Baker faces scale during 7 consecutive days after 8 weeks of therapy compared to baseline	4 weeks, 8 weeks, 12 weeks
Secondary	Change in Quality of Life	Change in quality of live will be measured with the PedsQL after 8 weeks of therapy compared to baseline	8 weeks
Secondary	Change in depression and anxiety score	Depression and anxiety scores are measured by the Revised Anxiety and Depression Scale-short version (RCADS-25) after 8 weeks of therapy compared to baseline	8 weeks
Secondary	School absences during the treatment	Hours of school absence in the previous week are measured.	4 weeks, 8 weeks, 12 weeks
Secondary	Use of pain rescue medication during the treatment	Use of pain rescue medication like paracetamol or NSAIDs	4 weeks, 8 weeks, 12 weeks
Secondary	Expectancy of treatment	expectations of both parents separately of the treatment on a scale of 0 (no improvement) to 10 (very much improved)	0 weeks
Secondary	Expectancy of treatment	the child's expectations of the treatment on a scale of 0 (no improvement) to 10 (very much improved)	0 weeks
Secondary	Change in defecation pattern	Change in defecation pattern is recorded as the daily stool frequency and consistency according to the Bristol Stool Scale	4 weeks, 8 weeks, 12 weeks
Secondary	Adequate relief	patients will be asked whether they have adequate relief of IBS/FAP-NOS symptoms using a single question ("Did you have adequate relief of IBS/FAP-NOS symptoms (abdominal discomfort/pain, bowel habits, and other symptoms like nausea and bloating) over the past week?") scored on a dichotomous scale (Yes/No)	4 weeks, 8 weeks, 12 weeks
Secondary	Health status	the EQ-5D-Y is a standardised questionnaire on health-related quality of life and will be used in the cost-effectiveness and cost-utility analysis	8 weeks
Secondary	Costs	iMCQ and the iPCQ will be used to measure the direct and indirect costs due to health care utilization and work absenteeism by parents	8 weeks, 12 weeks
Secondary	Safety of peppermint oil	incidence of adverse events will be reported by the participants	4 weeks, 8 weeks, 12 weeks
Secondary	Ease of use of peppermint oil capsules, placebo capsules or peppermint sweets	Ease of use of capsules or sweets will be scored after 8 weeks using a 5-point Likert scale with the following statement: the pills were easy to use and swallow: strongly disagree/disagree/neither agree nor disagree/agree/strongly agree.	8 weeks
Secondary	Taste of peppermint oil capsules, placebo capsules or peppermint sweets	taste of capsules or sweets will be scored after 8 weeks using a Likert scale: I like the taste of the pills: strongly disagree/disagree/neither agree nor disagree/agree/strongly agree.	8 weeks
Secondary	Placebo genes	Several other single nucleotide polymorphisms (SNPs) were found to influence response to placebo treatment. Therefore, we will investigate whether SNPs in a candidate set of genes (previously associated with either the placebo response in adults) are related to either placebo response or treatment response in children with IBS or FAP-NOS.	0 weeks