Expired Study
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Atlanta, Georgia 30328


Purpose:

Prospective, randomized, single site study to determine the safety and effectiveness of performing corneal collagen cross-linking (CCCL)using riboflavin and UVA light in eyes with corneal ectasia or progressive keratoconus.


Study summary:

Subjects are randomized to a control group or a treatment group, with the control group crossed over to the treatment group at the 3 month visit. Corneal collagen cross-linking is performed as a single treatment. Subjects are followed for at least 12 months to evaluate the long term effects of corneal collagen cross-linking. Subjects may be referred from other physicians but must return to Emory Vision for completion of all study visits.


Criteria:

Inclusion Criteria: - Diagnosis of keratoconus with documented progression over the previous 12 months. - Diagnosis of corneal ectasia - Must be able to complete all study visits Exclusion Criteria: - Prior corneal surgery in the keratoconus group - Corneal scarring


NCT ID:

NCT00567671


Primary Contact:

Principal Investigator
R. Doyle Stulting, MD, PhD
Emory Vision; Emory University


Backup Contact:

N/A


Location Contact:

Atlanta, Georgia 30328
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 21, 2017

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