Expired Study
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San Diego, California 92123


Purpose:

This study is designed to evaluate whether or not oral viscous budesonide is effective in treating children with Eosinophilic Esophagitis.


Criteria:

Inclusion Criteria: - Histologic evidence of EE defined as greater than 20 eosinophils per hpf on esophageal biopsy - Ages 1 yrs and older - Ability to continue the same diet that the patient was on at the time of EGD with biopsy Exclusion Criteria: - Adverse reaction or allergy to budesonide - Pregnancy - Chronic diseases requiring immunomodulatory therapy - Use of swallowed topical corticosteroids for EE within the past 3 months - Use of systemic steroids 2 months prior to study entry - Upper gastrointestinal bleed within 4 months of study entry - Chronic use of medications that predispose to upper gastrointestinal bleeding including non-steroidal anti-inflammatory medications or anticoagulants - Evidence of adrenal suppression prior to study entry - Evidence of concurrent eosinophilic gastritis, enteritis, colitis, or proctitis - Recent changes in asthma or allergic rhinitis therapy for 3 months


NCT ID:

NCT00638456


Primary Contact:

Principal Investigator
Ranjan Dohil, MD
UCSD


Backup Contact:

N/A


Location Contact:

San Diego, California 92123
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 19, 2018

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