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NCT00447577 · ClinicalTrials.gov registry record · Phase 4

Zylet vs TobraDex in Blepharokeratoconjunctivitis

A Phase 4 study, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
Phase 4
Development phase
276
Enrollment target

NCT00447577: Completed Phase 4 study, sponsored by Bausch & Lomb Incorporated.

NCT00447577 is a Phase 4 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 276 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00447577, a Phase 4 study, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 4
Development phase
276 participants
Enrollment target

Study Summary

The objective of this study is to evaluate the safety and efficacy of Zylet vs. Tobradex in the treatment of ocular inflammation associated with blepharokeratoconjunctivitis

Interventions

  • DRUG Loteprednol etabonate and tobramycin ophthalmic suspension
  • DRUG Tobramycin and dexamethasone ophthalmic suspension

Trial Details

FieldValue
Enrollment Target 276 participants
Start Date 2007-01
Est. Completion 2007-06
Phase Phase 4
Bausch & Lomb Incorporated

174 total trials

What the finished NCT00447577 record still lists

NCT00447577 is an interventional study that assigns participants to a tested intervention. The registered 276 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 (47% lower).

The record links to 0 conditions, and to 2 interventions - of which Loteprednol etabonate and tobramycin ophthalmic suspension is the first listed.

NCT00447577 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00447577 about?

NCT00447577 is a clinical study titled "Zylet vs TobraDex in Blepharokeratoconjunctivitis". The objective of this study is to evaluate the safety and efficacy of Zylet vs. Tobradex in the treatment of ocular inflammation associated with blepharokeratoconjunctivitis

What is the current status of trial NCT00447577?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 276 participants. The study started on 2007-01. Estimated completion is 2007-06.

What interventions are being tested in trial NCT00447577?

The interventions under investigation include: Loteprednol etabonate and tobramycin ophthalmic suspension (DRUG), Tobramycin and dexamethasone ophthalmic suspension (DRUG).

Who is sponsoring clinical trial NCT00447577?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00447577's enrollment target sits among peer trials

276 310th of 2000 higher than 1,690 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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Source: ClinicalTrials.gov NCT00447577, the US trial registry maintained by the National Library of Medicine. NCT00447577 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.