Expired Study
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Lexington, Kentucky


Purpose:

This study will assess the safety and utility of the new inserter for the administration of ILUVIEN in subjects with diabetic macular edema who have previously received either dose of the fluocinolone insert in the FAME studies.


Criteria:

Inclusion Criteria: - FAME study subjects - In the judgment of the Investigator, the subject will benefit from retreatment with ILUVIEN. Exclusion Criteria: - Retinal or choroidal neovascularization due to ocular conditions other than diabetic retinopathy - Glaucoma, defined as glaucomatous anatomical changes of the optic disc and/or visual field changes at screening in the study eye - History of uncontrolled IOP elevation with steroid use that did not respond to topical therapy or IOP-lowering procedure


NCT ID:

NCT01304706


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Lexington, Kentucky
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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