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NCT02125851 · ClinicalTrials.gov registry record · NA
Comparison of Esophageal Clearance Times of Oral Budesonide Preparations
A NA study, sponsored by Walter Reed National Military Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 24
- Enrollment target
NCT02125851: Completed NA study, sponsored by Walter Reed National Military Medical Center.
NCT02125851 is a NA study that has completed, run by Walter Reed National Military Medical Center. The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02125851, a NA study, has completed, sponsored by Walter Reed National Military Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 24 participants
- Enrollment target
Study Summary
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.
Primary Outcome
Comparison of esophageal contact time of sucralose slurry vs either honey slurry or xanthan gum based slurry. 1 hour will elapse between ingestions.
Interventions
- OTHER Honey
- OTHER Xanthan Gum
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2014-01 |
| Est. Completion | 2014-02 |
| Phase | NA |
What the finished NCT02125851 record still lists
NCT02125851 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 2 interventions - of which Honey is the first listed.
NCT02125851 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02125851 about?
NCT02125851 is a clinical study titled "Comparison of Esophageal Clearance Times of Oral Budesonide Preparations". 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.
What is the current status of trial NCT02125851?
This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2014-01. Estimated completion is 2014-02.
What interventions are being tested in trial NCT02125851?
The interventions under investigation include: Honey (OTHER), Xanthan Gum (OTHER).
Who is sponsoring clinical trial NCT02125851?
This trial is sponsored by Walter Reed National Military Medical Center, which has 48 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02125851's enrollment target sits among peer trials
24 1736th of 2000 higher than 246 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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