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NCT00905450 · ClinicalTrials.gov registry record · Phase 2

Evaluation of BOL-303242-X Versus Vehicle for the Treatment of Inflammation Following Cataract Surgery

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

Completed
Registry status
Phase 2
Development phase
415
Enrollment target

NCT00905450: Completed Phase 2 study, sponsored by Bausch & Lomb Incorporated.

NCT00905450 is a Phase 2 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 415 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (212% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00905450, a Phase 2 study, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 2
Development phase
415 participants
Enrollment target

Study Summary

This clinical study is being conducted to identify the most effective drug concentration and dose frequency of BOL-303242-X (Mapracorat) ophthalmic suspension, for the treatment of inflammation following cataract surgery.

Primary Outcome

Anterior chamber (AC) cells will be assessed using a 0 to 4 grading scale by an ophthalmologist using slip lamp biomicroscopy. A slit lamp examination of the lids, conjunctiva, limbus, cornea, anterior chamber, vitreous, and lens was performed without pupil dilation. Accumulation of white blood cells in aqueous was assessed. Pigment cells and red blood cells are to be ignored. The grades were defined as: 0 = No cells seen; 1 = 1 - 5 cells; 2 = 6 - 15 cells; 3 = 16 - 30 cells; 4 = \>30 cells. Com

Interventions

  • DRUG BOL-303242-X
  • DRUG Vehicle for BOL-303242-X

Trial Details

FieldValue
Enrollment Target 415 participants
Start Date 2009-06
Est. Completion 2010-05
Phase Phase 2
Bausch & Lomb Incorporated

174 total trials

What the finished NCT00905450 record still lists

NCT00905450 is an interventional study that assigns participants to a tested intervention. The registered 415 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 (212% higher).

The record links to 0 conditions, and to 2 interventions - of which BOL-303242-X is the first listed.

NCT00905450 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00905450 about?

NCT00905450 is a clinical study titled "Evaluation of BOL-303242-X Versus Vehicle for the Treatment of Inflammation Following Cataract Surgery". This clinical study is being conducted to identify the most effective drug concentration and dose frequency of BOL-303242-X (Mapracorat) ophthalmic suspension, for the treatment of inflammation following cataract surgery.

What is the current status of trial NCT00905450?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 415 participants. The study started on 2009-06. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00905450?

The interventions under investigation include: BOL-303242-X (DRUG), Vehicle for BOL-303242-X (DRUG).

Who is sponsoring clinical trial NCT00905450?

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 NCT00905450's enrollment target sits among peer trials

415 93rd of 2000 higher than 1,908 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 NCT00905450, the US trial registry maintained by the National Library of Medicine. NCT00905450 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.