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Corneal Collagen Cross-Linking for the Treatment of Progressive Keratoconus and Corneal Ectasia — CL  

Corneal Ectasia Clinical Trial

Official title:
Safety and Effectiveness of the UV-X System for Corneal Collagen Cross-Linking in Eyes With Corneal Ectasia or Progressive Keratoconus

Clinical Trial Summary

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.

Clinical Trial Description

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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00567671
Study type Interventional
Source Emory University
Contact
Status Completed
Phase Phase 2/Phase 3
Start date December 2007
Completion date June 2010
View Details
See also
  Status Clinical Trial Phase
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Terminated NCT01459679 - Safety & Efficacy of Corneal Collagen Cross-Linking in Eyes With Keratoconus or Corneal Ectasia After Refractive Surgery Phase 3
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Active, not recruiting NCT04698590 - Wavefront Guided Scleral Lenses for Keratoconus and Irregular Astigmatism N/A
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