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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 is a NA study that has completed, run by Walter Reed National Military Medical Center. The registered enrollment target is 24 participants.

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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.

Interventions

  • OTHER Honey
  • OTHER Xanthan Gum

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2014-01
Est. Completion 2014-02
Phase NA

What the Registry Record Tells You About NCT02125851

The ClinicalTrials.gov registry entry for NCT02125851 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Walter Reed National Military Medical Center, which has 48 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Honey is the first listed.

NCT02125851 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.