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NCT00705159 · ClinicalTrials.gov registry record · Phase 4
Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis
A Phase 4 study, sponsored by Bausch & Lomb Incorporated.
- Completed
- Registry status
- Phase 4
- Development phase
- 137
- Enrollment target
NCT00705159: Completed Phase 4 study, sponsored by Bausch & Lomb Incorporated.
NCT00705159 is a Phase 4 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 137 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (74% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00705159, a Phase 4 study, has completed, sponsored by Bausch & Lomb Incorporated.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 137 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the safety and effectiveness of Zylet in comparison with Lotemax, Tobramycin and the vehicle of Zylet for the treatment of blepharoconjunctivitis in pediatric subjects.
Primary Outcome
Change from baseline to visit 4 in the total blepharoconjunctivitis grade. Graded on a scale of 0-4, 0 (none), 1 (minimal/trace), 2 (mild), 3 (moderate), and 4 (severe). Grade range from 0-32.
Interventions
- DRUG Tobramycin
- DRUG loteprednol etabonate
- DRUG loteprednol etabonate and tobramycin
- DRUG Vehicle of Zylet
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 137 participants |
| Start Date | 2008-06 |
| Est. Completion | 2010-05 |
| Phase | Phase 4 |
What the finished NCT00705159 record still lists
NCT00705159 is an interventional study that assigns participants to a tested intervention. The registered 137 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (74% lower).
The record links to 0 conditions, and to 4 interventions - of which Tobramycin is the first listed.
NCT00705159 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00705159 about?
NCT00705159 is a clinical study titled "Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis". The objective of this study is to evaluate the safety and effectiveness of Zylet in comparison with Lotemax, Tobramycin and the vehicle of Zylet for the treatment of blepharoconjunctivitis in pediatric subjects.
What is the current status of trial NCT00705159?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 137 participants. The study started on 2008-06. Estimated completion is 2010-05.
What interventions are being tested in trial NCT00705159?
The interventions under investigation include: Tobramycin (DRUG), loteprednol etabonate (DRUG), loteprednol etabonate and tobramycin (DRUG), Vehicle of Zylet (DRUG).
Who is sponsoring clinical trial NCT00705159?
This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00705159's enrollment target sits among peer trials
137 594th of 2000 higher than 1,405 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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