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NCT00198536 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome

A Phase 2 study, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
Phase 2
Development phase
159
Enrollment target

NCT00198536: Completed Phase 2 study, sponsored by Bausch & Lomb Incorporated.

NCT00198536 is a Phase 2 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 159 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00198536, a Phase 2 study, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 2
Development phase
159 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether ecabet ophthalmic solution is an effective treatment for dry eye syndrome

Primary Outcome

Group mean change in ocular discomfort score from pre-Cataract extraction (CAE) to post-CAE

Interventions

  • DRUG Vehicle
  • DRUG Ecabet 2.83%
  • DRUG Ecabet 3.70%

Trial Details

FieldValue
Enrollment Target 159 participants
Start Date 2005-04
Est. Completion 2005-12
Phase Phase 2
Bausch & Lomb Incorporated

174 total trials

What the finished NCT00198536 record still lists

NCT00198536 is an interventional study that assigns participants to a tested intervention. The registered 159 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher).

The record links to 0 conditions, and to 3 interventions - of which Vehicle is the first listed.

NCT00198536 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00198536 about?

NCT00198536 is a clinical study titled "Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome". The purpose of this study is to determine whether ecabet ophthalmic solution is an effective treatment for dry eye syndrome

What is the current status of trial NCT00198536?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 159 participants. The study started on 2005-04. Estimated completion is 2005-12.

What interventions are being tested in trial NCT00198536?

The interventions under investigation include: Vehicle (DRUG), Ecabet 2.83% (DRUG), Ecabet 3.70% (DRUG).

Who is sponsoring clinical trial NCT00198536?

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 NCT00198536's enrollment target sits among peer trials

159 442nd of 2000 higher than 1,558 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00198536, the US trial registry maintained by the National Library of Medicine. NCT00198536 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.