Status:
TERMINATED
Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant
Lead Sponsor:
Bausch & Lomb Incorporated
Conditions:
Non-infectious Uveitis
Eligibility:
All Genders
6+ years
Phase:
PHASE2
PHASE3
Brief Summary
This is a multi-center, randomized, double-masked, controlled study to evaluate the safety and efficacy of fluocinolone acetonide intravitreal implants for the management of subjects with non-infectio...
Eligibility Criteria
Inclusion
- 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,
- Had clinically 'quiet' eyes at surgery.
Exclusion
- Coexistent medical or ocular conditions that would interfere with obtaining or interpreting data for this study.
Key Trial Info
Start Date :
May 1 2002
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2006
Estimated Enrollment :
239 Patients enrolled
Trial Details
Trial ID
NCT00456482
Start Date
May 1 2002
End Date
April 1 2006
Last Update
December 8 2011
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