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Completed

NCT Number: NCT00271349

Budesonide for Eosinophilic Esophagitis

Eosinophilic Esophagitis (EE) is a chronic, T-helper 2 cell (TH2) - type inflammatory disorder of the esophagus with a rapidly increasing prevalence. Studies analyzing the natural course of EE provide strong evidence, that the chronic inflammation leads to irreversible structural changes in the esophagus with a loss of the mucosal elasticity and a fibrosis of the sub-epithelial esophageal layers with a concomitant risk of impairment in function.

Treatment strategies in chronic inflammations have, in general, two main goals: 1) Relief of symptoms and 2) Prevention of long-term damage of the affected organ. Until now, the treatment of EE is still controversial. Standard recommendations for therapy of this chronic eosinophilic inflammation include dilation, systemic or topical corticosteroids and leukotriene antagonists. Several of these reports demonstrate, that topical corticosteroids may be effective for symptom control as well as for down-regulating the local inflammation. Furthermore it has been demonstrated, that treatment with topical corticosteroids is as effective as oral prednisone. However, the majority of therapeutic recommendations are based on clinical observations, case reports or small case series.

The purpose of this study is the evaluation of the efficacy and the safety of a monotherapy with a topical corticosteroid as short-term induction-treatment and as long-term, maintenance-treatment compared with placebo, in the treatment of adult patients with active EE.

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Key information

Age range

14 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of Gastroenterology, Kantonsspital

Olten, Canton of Solothurn, 4600, Switzerland

About this study

A randomized, double-blind, placebo-controlled, single center clinical trial to evaluate the efficacy and safety of topically applied Budesonide in the treatment of adult patients with Eosinophilic Esophagitis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Isolated Eosinophilic Esophagitis
  • Adult patients (age > 14 years)
  • Active disease (clinically and histologically)
  • Informed Consent

Exclusion criteria

  • Current use of specific treatments for EE
  • Secondary causes of esophageal eosinophilia
  • Intolerance to Budesonide
  • Concomitant therapies for any reason that may affect assessment
  • Use of an investigational drug with 30 days of entering the study
  • Recent history or suspicion of current drug abuse and alcohol abuse
  • Positive serum pregnancy test at the screening visit
  • Any unstable serious co-existing medical condition

Treatment and study plan

Budesonide

Drug

Primary outcomes

  1. Efficacy of Budesonide in inducing a reduction of the esophageal eosinophilic infiltration in adult individuals with active EE after 2 weeks of induction-treatment.

  2. Efficacy of Budesonide in sustaining a reduction of the esophageal eosinophilic infiltration in adult individuals with quiescent EE after 50 weeks of maintenance-treatment.

Secondary outcomes

  1. Efficacy of Budesonide in inducing a reduction of the clinical manifestations of active EE after 2 weeks of induction-treatment.

  2. Efficacy of Budesonide in sustaining a reduction of the clinical manifestations of quiescent EE after 50 weeks of maintenance-treatment.

  3. Efficacy of a one year treatment with Budesonide on esophageal remodeling in adult subjects with EE.

Sponsors and collaborators

Lead sponsor

Swiss EE Study Group

Other

Registry information

Official study title

Budesonide for Eosinophilic Esophagitis: a Randomized, Placebo-controlled, Double-blind Treatment Study

Acronym: BEE

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Dec 30, 2005
Registry last updated
May 22, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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