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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, pachymetry, and visual function questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04094090
Study type Interventional
Source Goodman Eye Center
Contact
Status Recruiting
Phase Phase 2
Start date October 19, 2019
Completion date December 19, 2024

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