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Completed

NCT Number: NCT03295747

Peppermint Oil Pharmacokinetics/Dynamics and Novel Biological Signatures in Children With Functional Abdominal Pain

Aim 1 - Determine the pharmacokinetics of PMO (menthol) of three different doses in children with functional abdominal pain (FAP) (n=30).

Aim 2 - Determine pharmacodynamic effect of three different doses of PMO on gut microbiome composition and contractile activity/gut transit rate.

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Key information

Age range

7 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Texas Children's Hospital

Houston, Texas, 77030, United States

About this study

Children with functional abdominal pain (FAP) ages 7-12 years (n=30) will be recruited.

The study participants will be admitted to the Children's Nutrition Research Center. A medical history and a general physical examination performed by the investigator or the research nurse. The height, weight, and vital signs (pulse rate, respiratory rate, and seated blood pressure) will be obtained. After application of a topical anesthetic to the site chosen for study-related blood sampling, a cannula will be inserted e to obtain repeated blood samples.

At approximately 0900, subjects will receive one of three doses of PMO as a single oral dose. Immediately prior to administration of the PMO, a blood sample will be obtained to measure total menthol concentration and leukocytes for isolation of DNA for CYP2A6 and UGT2B7 genotyping.

After PMO administration, repeated blood samples will be obtained over 24 hours.

At 2 hours after PMO administration, participants will be given a standardized meal and will eat ad libitum thereafter.

After completion of the final (24 hours) blood samples, vital signs will be reassessed and the venous cannula removed. Parents will receive a follow-up call from the research coordinator to access/evaluate if any adverse effects from dose or blood sampling received at the overnight study visit.

Prior to and after administration of peppermint oil (PMO) for 1 week at the dose defined above, children will undergo measurement of gut microbiome composition and GI motility and transit time. At the time of the stool collection, the child will also keep a 3 day diet history.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children ages 7-12 years old
  • They will be able to complete the protocol
  • A child will be recruited if the medical evaluation reveals no organic reason for the abdominal pain

Exclusion criteria

  • Children who have had past bowel surgery;
  • A child with documented GI disorders (e.g., Crohn's disease);
  • A child with a serious chronic medical condition (e.g., diabetes);
  • A child with a weight and/or height < 2 SD for age;
  • Children with chronic conditions with GI symptoms (e.g., cystic fibrosis);
  • Children with autism spectrum disorder, significant developmental delay, psychosis, depression, or a history of bipolar disorder;
  • Children who have been treated with antibiotics/probiotics within 2 mo. (because of effects on microbiome analysis).
  • Children who speak only Spanish

Treatment and study plan

Peppermint oil

Drug

Three doses of peppermint oil will be investigated: 180, 360, 540 mg; i.e. three arms.

Other names: Enteric coated peppermint oil capsules

Primary outcomes

  1. Pharmacokinetics

    Time frame: 24 hours

    Area under the curve

Secondary outcomes

  1. Contractility

    Time frame: Prior to and during peppermint oil treatment

    Number and amplitude of gut contractions as measured by SmartPill

  2. Gut Microbiome Composition

    Time frame: Prior to and during peppermint oil treatment

    Microbiome is defined for this study as a statistically significant change from baseline after treatment with PMO, correcting for multiple testing (q value). Such changes may occur with respect to gut microbiome diversity and/or composition (e.g., phylum, family, genera). We anticipate there will be an increased bacterial diversity, as well as increases in the abundance of organisms associated with a healthy microbiome, in response to PMO administration.

  3. Motility

    Time frame: Prior to and during peppermint oil treatment

    Gut transit time as measured by SmartPill

Sponsors and collaborators

Lead sponsor

Robert Shulman, M.D.

Other

Registry information

Acronym: PMO

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Sep 28, 2017
Registry last updated
Apr 6, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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