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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


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

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