Clinical Trial of Laser Custom Corneal Collagen Cross-Linking in Keratoconus

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Optical Coherence Tomography (OCT) devices are non-contact instruments that can measure the depth of scars, other causes of cloudiness of the cornea, and degree of corneal thinning in patients with keratoconus. Laser Custom Corneal Collagen Cross-linking (CXL) significantly decreases corneal aberrations and improves vision. This study will use OCT-guided setting for the lasers used in the corneal smoothing portion of the laser custom CXL procedure to assess the affect on visual outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of keratoconus

• Minimum corneal thickness of 410 microns

Locations
United States
Oregon
Oregon Health & Science University
RECRUITING
Portland
Contact Information
Primary
Denzil Romfh, OD
romfhd@ohsu.edu
503-494-4351
Backup
Humberto Martinez, COT
martinhu@ohsu.edu
503-494-7712
Time Frame
Start Date: 2018-06-20
Estimated Completion Date: 2027-12
Participants
Target number of participants: 100
Treatments
Experimental: Surgery
OCT-guided custom laser CXL
Related Therapeutic Areas
Sponsors
Collaborators: National Eye Institute (NEI)
Leads: Oregon Health and Science University

This content was sourced from clinicaltrials.gov