Ketotifen for Children With Functional Dyspepsia in Association With Duodenal Eosinophilia

Last updated: April 8, 2025
Sponsor: Children's Mercy Hospital Kansas City
Overall Status: Active - Recruiting

Phase

3

Condition

Stomach Discomfort

Non-ulcer Dyspepsia (Nud)

Heartburn (Pediatric)

Treatment

Ketotifen

Placebo

Clinical Study ID

NCT02484248
14110467
  • Ages 8-17
  • All Genders

Study Summary

Acid reduction remains the most common treatment prescribed empirically by pediatric gastroenterologists for children with functional dyspepsia (FD). When acid reduction therapy fails to provide patients with a therapeutic effect, ketotifen and cromolyn, mast cell stabilizers, represent an attractive potential therapy given data implicating mast cells in the generation of dyspeptic symptoms. Although there have been no adult or pediatric studies on the use of mast cell stabilizers in patients with FD, benefit has been demonstrated in adults with IBS and children with eosinophilic gastroenteritis. Additionally, previous studies show mucosal eosinophilia is highly correlated with functional dyspepsia. Our usual current treatment pathway for functional dyspepsia in association with duodenal mucosal eosinophilia is as follows: acid-reducing medication/montelukast → addition of H1 antagonist → addition of budesonide → addition of oral cromolyn. If ketotifen is effective, it offers the advantage of being able to replace both the H1 antagonist and the oral cromolyn at a substantially reduced cost (approximately 10% of the cost of cromolyn alone). This study aims to introduce ketotifen earlier in the treatment pathway to examine its efficacy on children with functional dyspepsia in association with duodenal eosinophilia.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. between the ages of 8 and 17 years, inclusive

  2. abdominal pain of at least 8 weeks duration and fulfilling symptom-based criteriafor functional dyspepsia(5);

  3. previous endoscopy with biopsies demonstrating >20 eosinophils/high powered fieldon duodenal mucosal biopsies;

  4. previous treatment with acid-reduction therapy and montelukast with a level 3 (asdefined below)or lesser response;

  5. evidence of written parental permission (consent) and subject assent;

  6. Negative pregnancy screening for females of child bearing potential.

Exclusion

Exclusion Criteria:

  1. previous treatment with ketotifen;

  2. treatment with oral corticosteroids or oral cromolyn sodium in the 6 months prior toenrollment;

  3. any prior history of diabetes mellitus, cancer, chronic cardiac disease, respiratorydisease, or renal disease requiring routine medical care;

  4. Pregnant/planning to become pregnant;

  5. Post-menarche females unwilling to use highly-efficacious contraception to preventpregnancy;

  6. Epilepsy or history of seizures;

  7. Liver disease or elevation of liver enzymes;

  8. Use of oral hypoglycemic medications, antipsychotics, benzodiazepines, tricyclicantidepressants, barbiturates, or opioids;

  9. Allergy to ketotifen or other products in capsule

  10. Refusal of Urine pregnancy test in post-menarchal females.

Study Design

Total Participants: 40
Treatment Group(s): 2
Primary Treatment: Ketotifen
Phase: 3
Study Start date:
August 01, 2015
Estimated Completion Date:
April 01, 2027

Study Description

This study is a double-blind, placebo-controlled, cross-over trial of ketotifen in children ages 8 through 17 inclusive that have a diagnosis of functional dyspepsia and have had continued abdominal pain despite acid reduction therapy in combination with montelukast. The primary aim is to assess the symptomatic response to ketotifen as compared to placebo in children with functional dyspepsia in association with duodenal eosinophilia who have previously had worsening, no clinical change, or only a partial response to acid-reduction therapy in combination with montelukast.

The study lasts 147 days for subjects responsive to ketotifen and 63 days for those who are not. For those who respond to ketotifen, there are 4 clinic visits and 3 phone interviews. Clinic visits include a physical, blood draws, questionnaires, review of medical history and medications; phone interviews involve answering a few questions. For those who do not respond to ketotifen, there are 3 clinic and 2 phone visits. Subjects who enroll in the study are randomly assigned to Group A or Group B. The subject, subject's parents, and study staff will not know to which group the subject is assigned. Group A will be given a placebo, an inactive pill with no medication in it, for days 1-28, and switched to ketotifen for days 36-63. Group B will be given ketotifen for days 1-28 and switched to placebo for days 36-63. The group assignment will be unblinded at day 63, at which point initial ketotifen responders will undergo an open-label twelve week trial of ketotifen to assess sustainability.

Secondary aims include: 1) assessing the impact of ketotifen as compared to placebo on quality of life; 2) assessing the sustainability of response to ketotifen in initial responders, and 3) assessing the pharmacokinetics of ketotifen in this patient population.

Connect with a study center

  • The Children's Mercy Hospital

    Kansas City, Missouri 64108
    United States

    Active - Recruiting

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