Actively Recruiting

Phase Not Applicable
Age: 1Year - 21Years
All Genders
NCT07234825

Trial of Partial Enteral Nutrition With Dairy Free Diet in Eosinophilic Esophagitis

Led by Kate Farms Inc · Updated on 2026-04-16

36

Participants Needed

1

Research Sites

145 weeks

Total Duration

On this page

Sponsors

K

Kate Farms Inc

Lead Sponsor

S

Seattle Children's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to introduce a new dietary therapy for Eosinophilic Esophagitis (EoE) patients by using partial enteral nutrition (PEN) to enhance remission rates and explore how this approach affects immune function, gut microbiota, and environmental toxin exposures.

CONDITIONS

Official Title

Trial of Partial Enteral Nutrition With Dairy Free Diet in Eosinophilic Esophagitis

Who Can Participate

Age: 1Year - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pediatric patients aged 1 year to 21 years
  • Chronic symptoms such as difficulty swallowing, painful swallowing, vomiting, heartburn, abdominal pain, weight loss, or picky eating
  • Planning to undergo endoscopy (EGD) for evaluation
  • Presenting to outpatient gastroenterology clinic
Not Eligible

You will not qualify if you...

  • Non-English-speaking individuals
  • Adults unable to consent
  • Wards of the state
  • Pregnant women
  • Prisoners
  • Patients with autoimmune conditions like inflammatory bowel disease
  • Patients with prior esophageal or intestinal surgeries
  • Patients with history of eating disorders or Avoidant/Restrictive Food Intake Disorder (ARFID)
  • Patients with fistulizing or fibrotic disease on baseline endoscopy
  • Patients who received proton pump inhibitor therapy in the past month

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Seattle Children's Hospital

Seattle, Washington, United States, 98105

Actively Recruiting

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Research Team

D

Danny Gagucas

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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