CompletedNot applicableNCT00952614
A Study of a Sustained Release Fluocinolone Implant for Treatment of Central Retinal Vein Occlusion
Studying Central retinal vein occlusion
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
- Glenn Jaffe
- Principal Investigator
- Glenn J Jaffe, MDDuke Eye Center, DUMC
- Intervention
- fluocinolone acetonide (Retisert Implant, Bausch and Lomb)(device)
- Enrollment
- 29 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2002 – 2009
Study locations (1)
- Duke Eye Center, Durham, North Carolina, United States
Collaborators
Bausch & Lomb Incorporated
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.
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