Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implants

Completed · Phase 2/Phase 3

Conditions studied: Noninfectious Posterior Uveitis

In brief

This is a multi-center, randomized, double-masked, controlled study to evaluate the safety and efficacy of fluocinolone acetonide (FA) intravitreal implants for the management of subjects with non-infectious uveitis affecting the posterior segment of the eye. An additional objective is to compare the safety and efficacy of two doses of fluocinolone acetonide.

Key facts

Study ID

NCT00407082

Run by

Bausch & Lomb Incorporated

People needed

278

Starts

2000-12-01

Expected to finish

2005-09-01

Last updated by the study team

2011-12-08

Who can join

Age: 6 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males or non-pregnant females at least 6 years of age who had been diagnosed and treated for recurrent, non-infectious uveitis affecting the posterior segment of one or both eyes for at least 1 year prior to the start of the study, and had 'quiet' eyes at surgery

You may not qualify if…

• Coexisting medical or ocular conditions that would interfere with the study results

Where it is running

• Duke Eye Center — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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