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Safety and Efficacy of Corneal Crosslinking Using the PXL-Platinum 330 for Eyes With Corneal Ectatic Conditions

Keratoconus Clinical Trial

Official title:
Safety and Effectiveness of the PXL-Platinum 330 System for Corneal Crosslinking in Eyes With Corneal Ectatic Conditions

Clinical Trial Summary

To evaluate the safety and effectiveness of the PXL Platinum 330 device for performing Corneal Crosslinking in patients 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, intraocular pressure and visual function questionnaire assessments. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04240457
Study type Interventional
Source Arbor Center for Eye Care
Contact
Status Terminated
Phase Phase 2
Start date July 8, 2020
Completion date February 18, 2023
View Details
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