Eosinophilic Esophagitis Clinical Trial
Official title:
Prospective Pilot Study Evaluating the Efficacy of Low-Dose Topical Steroids in Maintaining Histologic Remission of Eosinophilic Esophagitis in Children
NCT number | NCT05309590 |
Other study ID # | 2014-15753 |
Secondary ID | |
Status | Active, not recruiting |
Phase | |
First received | |
Last updated | |
Start date | May 2014 |
Est. completion date | May 2025 |
Verified date | August 2023 |
Source | Ann & Robert H Lurie Children's Hospital of Chicago |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
This study evaluates the decrease in steroid dosing for patients who have achieved remission on a full dose of steroids. Once a patient is in remission they will be enrolled in this study if they choose to decrease the steroid dosing.
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | May 2025 |
Est. primary completion date | May 2024 |
Accepts healthy volunteers | |
Gender | All |
Age group | 1 Year to 21 Years |
Eligibility | Inclusion Criteria: - Patients diagnosed with EoE - Patients less than 21 years of age at enrollment - Patients who within the past 12 months have demonstrated histologic remission (<15 eos/hpf as assessed by upper esophagogastroduodenoscopy (EGD) with biopsy ) to the standard induction dose of topical steroids and have remained on this treatment: - Topical steroid treatment includes only those with previously published results: Swallowed topical fluticasone (i.e. Flovent®), and Swallowed viscous budesonide (i.e. Pulmicort Respules®) mixed with Honey or Splenda® - Patients who are interested in lowering their dose of topical steroids. Exclusion Criteria: - Patients with EoE who have not demonstrated histologic remission (<15 eos/hpf) to topical steroids. - Patients who are unable or unwilling to take topical steroids. - Patients who have changed the vehicle or carrier (e.g. Splenda®or honey ) used to mix with the actual steroid drug, after demonstrating histologic remission. |
Country | Name | City | State |
---|---|---|---|
United States | Ann & Robert H Lurie Childjren's Hospital of Chicago | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Ann & Robert H Lurie Children's Hospital of Chicago |
United States,
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Efficacy of Low Dose Topical Steroid | Number of patients who maintain histologic remission of low dose (50% dosing) topical steroids | At standard of care endoscopies from the date of enrollment; estimated every 6-12 months | |
Secondary | Visual and histologic assessment of the esophagus | assess the change in visual findings on steroid or half dose steroid and whether patients were able to maintain visual and histologic remission when on low dose (50% dosing) topical steroids | At standard of care endoscopies from the date of enrollment; estimated every 6-12 months | |
Secondary | Determine medication adherence | data collected by the Morisky 8-item medication adherence questionnaire will be analyzed to see if adherence is a factor in remission | At standard of care endoscopies from the date of enrollment; estimated every 6-12 months |
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