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Safety and Effectiveness of the PXL-Platinum 330 System

Keratoconus Clinical Trial

Official title:
Safety and Effectiveness of the PXL-Platinum 330 System for Corneal Collagen Cross-Linking in Eyes With Corneal Thinning Conditions

Clinical Trial Summary

To evaluate the safety and effectiveness of the PXL Platinum 330 system for performing corneal cross-linking (CXL) for the treatment of ectatic disorders.

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, intraocular pressure, and pachymetry. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04401865
Study type Interventional
Source Colorado Eye Consultants/Cornea Consultants of Colorado
Contact Shivam Patel, BS
Phone 720-709-7523
Email spatel@corneaonline.com
Status Recruiting
Phase Phase 1/Phase 2
Start date June 1, 2020
Completion date June 30, 2023
View Details
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