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NCT Number: NCT07779772

Elimination Diet Strategies and Histologic Remission in Children With Eosinophilic Gastrointestinal Disorders

This prospective observational cohort study aims to evaluate clinical and histologic outcomes of elimination diets in children aged 2-17 years with eosinophilic gastrointestinal disorders (EGIDs). The type of elimination diet will be determined by the treating physician as part of routine clinical care according to each patient's clinical characteristics. The study will not assign participants to a specific dietary treatment. Clinical symptoms, histologic findings, growth parameters, and nutritional outcomes will be prospectively recorded. Follow-up endoscopy and biopsies performed as part of routine clinical care will be used to assess histologic response. Food reintroduction and disease recurrence will also be evaluated during follow-up.

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Key information

Age range

2 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Cukurova University Balcali Hospital

Adana, Sarıcam, 01330, Turkey (Türkiye)

Location status: Recruiting

Location contact

Ali Islek, MD

CONTACT

[email protected]

903223386060 (158)

About this study

This is a prospective observational cohort study of children aged 2-17 years diagnosed with eosinophilic gastrointestinal disorders (EGIDs). Children undergoing upper and/or lower gastrointestinal endoscopy for clinical indications will be evaluated using multiple segment-specific biopsies. Patients with histologic eosinophilic infiltration consistent with an EGID, after exclusion of other relevant causes, will be eligible for inclusion.

Elimination diets used in routine clinical practice may include single-, two-, four-, or six-food elimination strategies involving commonly implicated foods such as milk, egg, soy, wheat, nuts/peanuts, and seafood. The type and extent of dietary elimination will be determined independently by the treating physician based on the patient's clinical history and clinical assessment. No dietary strategy will be assigned by the study protocol. Dietary management will be conducted with dietitian support, and nutritional status will be monitored.

Clinical symptoms, anthropometric measurements, laboratory parameters, endoscopic findings, and segment-specific histologic eosinophil counts will be prospectively recorded. Follow-up endoscopy with biopsies from the same gastrointestinal segments is planned as part of clinical care approximately 8-12 weeks after initiation of the elimination diet. Clinical and histologic responses to dietary treatment will be evaluated.

Patients achieving clinical and histologic remission will continue dietary management according to routine clinical care and will subsequently undergo planned food reintroduction. Foods will be reintroduced individually, and recurrence of symptoms and, when clinically indicated, histologic recurrence will be recorded. The study will also evaluate growth, nutritional safety, dietary adherence, and factors associated with clinical and histologic response. No additional invasive procedure will be performed solely for research purposes.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 2-17 years.
  • Presence of gastrointestinal symptoms such as abdominal pain, vomiting, diarrhea, hematemesis, or hematochezia.
  • Undergoing upper and/or lower gastrointestinal endoscopy for a clinical indication.
  • Histologic eosinophilic infiltration consistent with an eosinophilic gastrointestinal disorder.
  • Exclusion of other relevant causes of gastrointestinal eosinophilia.

Exclusion criteria

  • Inflammatory bowel disease, parasitic infection, celiac disease, drug-associated enteropathy, hypereosinophilic syndrome, or other identified causes of gastrointestinal eosinophilia.
  • Known primary immunodeficiency.
  • Active malignancy.
  • Systemic rheumatologic disease.

Treatment and study plan

Elimination Diet

Other

Elimination diets may include single-, two-, four-, or six-food elimination strategies involving milk, egg, soy, wheat, nuts/peanuts, and seafood. The dietary strategy is determined by the treating physician as part of routine clinical care based on each patient's clinical characteristics. The study protocol does not assign or modify the dietary treatment.

Primary outcomes

  1. Combined Clinical and Histologic Remission

    Time frame: 8-12 weeks after initiation of the elimination diet

    Proportion of participants achieving both a clinically meaningful reduction in symptom score and histologic remission, defined as segment-specific eosinophil counts decreasing below the predefined histologic threshold.

Secondary outcomes

  1. Change in Weight Standard Deviation Score (SDS)

    Time frame: Baseline and 12 months

    Change in weight-for-age standard deviation score (SDS) from baseline to 12 months.

  2. Change in Height Standard Deviation Score (SDS)

    Time frame: Time Frame: Baseline and 12 months

    Change in height-for-age standard deviation score (SDS) from baseline to 12 months.

  3. Change in Body Mass Index Standard Deviation Score (BMI SDS)

    Time frame: Baseline and 12 months

    Change in body mass index standard deviation score (BMI SDS) from baseline to 12 months.

  4. Number of Participants With Iron Deficiency During Elimination Diet

    Time frame: Up to 12 months

    Number of participants with iron deficiency identified during elimination diet therapy based on serum iron measurements obtained as part of routine clinical care.

  5. Number of Participants With Vitamin B12 Deficiency During Elimination Diet

    Time frame: Up to 12 months

    Number of participants with vitamin B12 deficiency identified during elimination diet therapy based on serum vitamin B12 measurements obtained as part of routine clinical care.

  6. Number of Participants With Vitamin D Deficiency During Elimination Diet

    Time frame: Up to 12 months

    Number of participants with vitamin D deficiency identified during elimination diet therapy based on serum 25-hydroxyvitamin D measurements obtained as part of routine clinical care.

  7. Number of Participants With Anemia During Elimination Diet

    Time frame: Up to 12 months

    Number of participants with anemia identified during elimination diet therapy based on hemoglobin levels below the age- and sex-appropriate reference range.

  8. Recurrence After Food Reintroduction

    Time frame: Up to 12 months after initiation of food reintroduction

    Proportion of participants developing recurrence of gastrointestinal symptoms and, when clinically assessed, histologic recurrence following stepwise food reintroduction.

  9. Adherence to Elimination Diet

    Time frame: Up to 12 months

    Proportion of participants who remain adherent to the prescribed elimination diet during follow-up.

  10. Number of Participants With a Triggering Food Identified During Food Reintroduction

    Time frame: Through study completion, up to 24 months

    Number of participants in whom at least one individual food is identified as a triggering food based on recurrence of gastrointestinal symptoms following stepwise food reintroduction. Histologic recurrence will also be recorded when follow-up endoscopy and biopsy are clinically indicated.

Study contacts

Contact information is provided by the study sponsor or research team.

Ali Islek, MD

CONTACT

[email protected]

903223386060 (158)

Sponsors and collaborators

Lead sponsor

Cukurova University

Other

Registry information

Official study title

Elimination Diet Strategies, Histologic Remission, and Clinical Follow-Up in Children With Eosinophilic Gastrointestinal Disorders: A Prospective Cohort Study

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Aug 21, 2026
Registry last updated
Aug 21, 2026

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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