CompletedNCT01060787
Evaluation of Corneal Endothelial Cell Density in Subjects Who Have Had a Fluocinolone Acetonide Implant
Studying 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
- Johnson Varughese, PAValeant Pharmaceuticals/Bausch & Lomb
- Intervention
- Fluocinolone Acetonide 0.59 mg(procedure)
- Enrollment
- 98 target
- Eligibility
- 6 years · All sexes
- Timeline
- 2016 – 2019
Study locations (1)
- Ophthalmic Partners of Boston, Boston, Massachusetts, United States
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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