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Safety and Effectiveness of the PXL-Platinum 330 System for CXL Using Riboflavin Solution

Keratoconus Clinical Trial

Official title:
Evaluation of the Safety and Effectiveness of the PXL-Platinum 330 System for Corneal Collagen Cross-linking in Eyes With Corneal Thinning Conditions Using Peschke Riboflavin Solution

Clinical Trial Summary

Safety and Effectiveness of the PXL-Platinum 330 System for Corneal Collagen Cross-linking in Eyes With Corneal Thinning Conditions

Clinical Trial Description

Patients with progressive keratoconus, pellucid marginal degeneration, or at risk for post-refractive corneal ectasia will be recruited and undergo epithelial-on corneal crosslinking with the Peschke PXL-330 system using pulsed, accelerated energy delivery. Patients will undergo monitoring for 1 year, with serial measurements of corneal topography, visual acuity, pachymetry, and visual function. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04177082
Study type Interventional
Source Cornea Associates of Texas
Contact
Status Completed
Phase Phase 1
Start date January 10, 2020
Completion date May 5, 2022
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