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NCT00864396 · ClinicalTrials.gov registry record · Phase 1
Twice Daily Prevacid for the Treatment of Laryngopharyngeal Reflux
A Phase 1 study, sponsored by University of California, Davis.
- Completed
- Registry status
- Phase 1
- Development phase
- 59
- Enrollment target
NCT00864396: Completed Phase 1 study, sponsored by University of California, Davis.
NCT00864396 is a Phase 1 study that has completed, run by University of California, Davis. The registered enrollment target is 59 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00864396, a Phase 1 study, has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 59 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether treatment with twice-daily Lansoprazole 30mg (Prevacid 30mg) and behavioral modifications for reflux is superior to treatment with behavioral modifications for reflux alone in the treatment of laryngopharyngeal reflux (LPR).
Interventions
- DRUG Prevacid
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 59 participants |
| Start Date | 2005-07 |
| Est. Completion | 2008-05 |
| Phase | Phase 1 |
What the finished NCT00864396 record still lists
NCT00864396 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which Prevacid is the first listed.
NCT00864396 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00864396 about?
NCT00864396 is a clinical study titled "Twice Daily Prevacid for the Treatment of Laryngopharyngeal Reflux". The purpose of this study is to determine whether treatment with twice-daily Lansoprazole 30mg (Prevacid 30mg) and behavioral modifications for reflux is superior to treatment with behavioral modifications for reflux alone in the treatment of laryngopharyngeal reflux (LPR).
What is the current status of trial NCT00864396?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 59 participants. The study started on 2005-07. Estimated completion is 2008-05.
What interventions are being tested in trial NCT00864396?
The interventions under investigation include: Prevacid (DRUG).
Who is sponsoring clinical trial NCT00864396?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00864396's enrollment target sits among peer trials
59 895th of 2000 higher than 1,106 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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