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Comparison of Esophageal Clearance Times of Oral Budesonide Preparations

NCT02125851 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2014-04-29

No results posted yet for this 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.

Conditions

  • Eosinophilic Esophagitis

Interventions

OTHER

Xanthan Gum

esophageal mucosal contact time vs sucralose slurry

OTHER

Honey

esophageal mucosal contact time of honey vs sucralose slurry

Sponsors & Collaborators

  • Walter Reed National Military Medical Center

    lead FED

Principal Investigators

  • Jody N Hefner, DO · Walter Reed National Military Medical Center

Study Design

Allocation
RANDOMIZED
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2014-02-28
Completion
2014-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02125851 on ClinicalTrials.gov