CompletedPHASE2, PHASE3NCT00468871
Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant vs Standardized Therapy
Studying Posterior uveitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Bausch & Lomb Incorporated
- Principal Investigator
- Carlos Pavesio, MD, MDMedical Retina Service/Moorfields Eye Hospital
- Intervention
- fluocinolone acetonide intravitreal implant(drug)
- Enrollment
- 140 enrolled
- Eligibility
- 6 years · All sexes
- Timeline
- 2002 – 2006
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT00468871 on ClinicalTrials.gov