Clinical trial
Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant
NCT00456482 · Bausch & Lomb Incorporated, Industry · Terminated
Key facts
| NCT number | NCT00456482 |
|---|---|
| Title | Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant |
| Official title | A Multicenter, Randomized, Double-Masked, Controlled Study to Evaluate the Safety and Efficacy of an Intravitreal Fluocinolone Acetonide Implant in Subjects With Non-Infectious Uveitis Affecting the Posterior Segment of the Eye |
| Lead sponsor | Bausch & Lomb Incorporated, Industry |
| Status | Terminated |
| Phase | Phase 2/Phase 3 |
| Study type | Interventional |
| Conditions | Non-infectious Uveitis |
| Intervention type | Drug |
| Interventions | Fluocinolone Acetonide 0.59mg, Fluocinolone Acetonide 2.1mg |
| Enrollment | 239 |
| Start date | May 1, 2002 |
| Primary completion | Apr 1, 2006 |
| Completion | Apr 1, 2006 |
| First posted | Apr 5, 2007 |
| Last update posted | Dec 8, 2011 |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: