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EoE Food Desensitization

Primary Purpose

Eosinophilic Esophagitis

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Oral food desensitization
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Eosinophilic Esophagitis focused on measuring oral food desensitization, food elimination, food reintroduction

Eligibility Criteria

3 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Pediatric patient, ages 3-17 years, with known diagnosis of EoE based upon esophageal biopsy demonstrating ≥15 eos/hpf and lack of symptomatic or histological response to PPI therapy and/or normal esophageal pH evaluation.
  2. Known or suspected flare-inducing food trigger based upon supporting histological evidence.
  3. Already undergoing a baseline EGD followed by food reintroduction and repeat EGD, as standard of care at the recommendation of the child's gastroenterologist.
  4. Signed informed consent for the subject's participation in the study provided by the parent/ legal guardian and child/adolescent assent for subjects 7-17 years.
  5. Assent by the patient's pediatric gastroenterologist for the patient's participation in the study.

Exclusion Criteria:

  1. Presence of other disorders associated with similar clinical, histological or endoscopic features, such as PPI-responsive esophageal eosinophilia, esophageal eosinophilia associated with gastroesophageal reflux disease (GERD), Crohn's disease, infectious esophagitis (i.e. herpes simplex virus or candida), drug-associated esophagitis, collagen vascular disease, hypereosinophilic syndrome and eosinophilic gastroenteritis.
  2. Previous or current diagnosis of cancer or leukemia.
  3. History of chemotherapy within the past 3 months.
  4. History of esophageal stricture or food impaction.
  5. History of anaphylaxis or other severe adverse reaction to the specific food trigger being tested.

Sites / Locations

  • University of Texas Health Science CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Oral food desensitization

Arm Description

All of the children enrolled in the study will receive oral food desensitization with his or her specific EoE flare-inducing food antigen (e.g. cow's milk protein). The food antigen will be diluted in a 50% glycerin/water solution containing ascorbic acid (Vitamin C) to stabilize and preserve the solution. This oral spray will need to be administered twice a day, every day for a total of 4 months.

Outcomes

Primary Outcome Measures

Peak eosinophil count on esophageal biopsy
Remission of esophageal eosinophilia as defined by having <15 eosinophils per high power field on peak esophageal biopsy

Secondary Outcome Measures

Full Information

First Posted
August 11, 2016
Last Updated
June 21, 2021
Sponsor
The University of Texas Health Science Center, Houston
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1. Study Identification

Unique Protocol Identification Number
NCT02881372
Brief Title
EoE Food Desensitization
Official Title
Safety and Feasibility of Oral Food Desensitization in Children With Eosinophilic Esophagitis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 8, 2018 (Actual)
Primary Completion Date
May 2023 (Anticipated)
Study Completion Date
May 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a single-center, prospective, pilot clinical trial in which children ages 3-17 years with eosinophilic esophagitis (EoE) who have a known food that triggers EoE flares receive oral desensitization with that specific food antigen, followed by reintroduction of that food into the diet. The purpose of this study is to investigate the safety and feasibility of oral desensitization in children with EoE so that, if determined to be safe, can be repeated on a larger scale to determine efficacy.
Detailed Description
Eosinophilic esophagitis (EoE) is a clinicopathologic disorder of the esophagus triggered by food and/or environmental allergens and is characterized by symptoms of esophageal dysfunction and eosinophilia of the esophagus. Current therapy is centered on controlling inflammation with steroids and/or food antigen avoidance. Such treatment options have significant side effects and reduce quality of life, especially in children. The purpose of the study is to discover a way for flare-provoking foods to be reintroduced into the child's diet without the need for medical therapy. The study would involve children ages 3-17 years with biopsy-proven EoE who have a known flare-inducing food trigger. Following baseline blood work and esophagogastroduodenoscopy (EGD), the investigators will initiate oral desensitization treatment in which the child swallows a spray solution containing his or her specific food allergen extract in increasing concentrations twice daily for 4 months. The next phase of the study would involve reintroduction of the actual food for 4 weeks followed by repeat blood work and EGD. Success would be defined by having a peak eosinophil count <15 per high power field on the final esophageal biopsy. Oral food desensitization has been well-studied in patients with food allergies but never in patients with pre-existing EoE. In those studies, the adverse events included mild reactions, such as watery eyes, rhinitis, sneezing, throat pruritus, transient erythema and abdominal pain. These reactions usually did not require stopping desensitization and were well controlled by antihistamines and steroids. Benefits include children having a less restricted diet and eliminating the need for steroid therapy. This study should yield valuable information regarding the management of EoE, thereby improving the current understanding of its pathogenesis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eosinophilic Esophagitis
Keywords
oral food desensitization, food elimination, food reintroduction

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Oral food desensitization
Arm Type
Experimental
Arm Description
All of the children enrolled in the study will receive oral food desensitization with his or her specific EoE flare-inducing food antigen (e.g. cow's milk protein). The food antigen will be diluted in a 50% glycerin/water solution containing ascorbic acid (Vitamin C) to stabilize and preserve the solution. This oral spray will need to be administered twice a day, every day for a total of 4 months.
Intervention Type
Other
Intervention Name(s)
Oral food desensitization
Intervention Description
The child's specific food antigen will be diluted in a 50% glycerin/water solution containing ascorbic acid (Vitamin C). This oral spray solution will need to be administered twice a day, every day for a total of 4 months
Primary Outcome Measure Information:
Title
Peak eosinophil count on esophageal biopsy
Description
Remission of esophageal eosinophilia as defined by having <15 eosinophils per high power field on peak esophageal biopsy
Time Frame
5 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pediatric patient, ages 3-17 years, with known diagnosis of EoE based upon esophageal biopsy demonstrating ≥15 eos/hpf and lack of symptomatic or histological response to PPI therapy and/or normal esophageal pH evaluation. Known or suspected flare-inducing food trigger based upon supporting histological evidence. Already undergoing a baseline EGD followed by food reintroduction and repeat EGD, as standard of care at the recommendation of the child's gastroenterologist. Signed informed consent for the subject's participation in the study provided by the parent/ legal guardian and child/adolescent assent for subjects 7-17 years. Assent by the patient's pediatric gastroenterologist for the patient's participation in the study. Exclusion Criteria: Presence of other disorders associated with similar clinical, histological or endoscopic features, such as PPI-responsive esophageal eosinophilia, esophageal eosinophilia associated with gastroesophageal reflux disease (GERD), Crohn's disease, infectious esophagitis (i.e. herpes simplex virus or candida), drug-associated esophagitis, collagen vascular disease, hypereosinophilic syndrome and eosinophilic gastroenteritis. Previous or current diagnosis of cancer or leukemia. History of chemotherapy within the past 3 months. History of esophageal stricture or food impaction. History of anaphylaxis or other severe adverse reaction to the specific food trigger being tested.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tu T Mai, MD
Phone
713-500-5663
Email
eoehouston@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Rhoads, MD
Organizational Affiliation
University of Texas
Official's Role
Study Director
Facility Information:
Facility Name
University of Texas Health Science Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tu T Mai, MD
Phone
713-500-5663
Email
eoehouston@gmail.com
First Name & Middle Initial & Last Name & Degree
Tu T Mai, MD

12. IPD Sharing Statement

Plan to Share IPD
No
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Links:
URL
http://wayback.archive-it.org/7993/20180123233947/https:/www.fda.gov/Food/IngredientsPackagingLabeling/GRAS/SCOGS/ucm260452.htm
Description
Select Committee on GRAS Substances (SCOGS) Opinion: L-ascorbic acid, sodium L-ascorbate, calcium L-ascorbate, ascorbyl palmitate (palmitoyl L-ascorbic), erythorbic acid (D-isoascorbic acid), and sodium erythorbate (sodium D-isoascorbate)

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EoE Food Desensitization

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