Esophageal String Test Monitoring to Monitor Eosinophilic Esophagitis During Oral Immunotherapy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age7-17
SponsorChildren's Hospital of Philadelphia

About this trial

Patients with IgE mediated food Allergy have elevated risk of eosinophilic esophagitis, and new therapies like oral immunotherapy (OIT) carry additional risk of Eosinophilic Esophagitis (EoE). The goal of this study is to investigate the Esophageal String Test (EST) as a screening tool for Eosinophilic Esophagitis (EoE) during OIT therapy. Investigators will compare the efficacy of the Esophageal String Test to symptom assessment using a validated patient reported symptom questionnaire, the Pediatric Eosinophilic Esophagitis Symptom Score (PEESS) v2.0. Investigators will utilize these tools to screen patients at their baseline visit prior to the start of OIT, then at the 3- and 6-month OIT follow-up visits.

Eligibility criteria

Qualifiers

Male or female, aged 7 to 18 years old, inclusive

Have a history of Immunoglobulin (IgE)-mediated food allergy

Considering using oral immunotherapy (OIT) for food allergies at CHOP°

Able & willing to swallow the esophageal capsule

Disqualifiers

Known or expected need for MRI imaging during the study period

Known connective tissue disease

Known eosinophilic disorder including any eosinophilic gastrointestinal disorder and hypereosinophilic disorder

Past history of caustic ingestion or other esophageal injury

Trial design

Treatments tested in this trial

  • Esophageal String Test

Treatment groups

75 Participants
are divided into 1 treatment group