Comparison of Esophageal Clearance Times of Oral Budesonide Preparations
Completed · Not applicable
Conditions studied: Eosinophilic Esophagitis
In brief
The purpose of this study is to determine if a xanthan gum or honey based budesonide slurry exhibit comparable mucosal contact time to a budesonide/sucralose slurry in healthy adult subjects.
Key facts
- Study ID
- NCT02125851
- Run by
- Walter Reed National Military Medical Center
- People needed
- 24
- Starts
- 2014-01-01
- Expected to finish
- 2014-02-01
- Last updated by the study team
- 2014-04-29
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- DEERS eligible
- Older than 18 y/o, without diagnosis of Eosinophilic Esophagitis or other esophageal disease
You may not qualify if…
- History of EoE, esophageal surgery or known achalasia/stricture or previously diagnosed GERD or GER that requires more frequent than once a week treatment.
- Peripheral eosinophil count above 0.5 X10\^3 / mcL.
- Pregnancy or breastfeeding
- Previous adverse reaction to budesonide, honey, or oranges.
Where it is running
- Walter Reed National Military Medical Center — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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