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Clinical Trial Summary

To determine whether the Peschke PXL-330 is safe and effective in the treatment of corneal thinning conditions.


Clinical Trial Description

Patients with progressive keratoconus, pellucid marginal degeneration, infectious keratitis, 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04213885
Study type Interventional
Source Eye Specialists of Indiana
Contact Clark L Springs, MD
Phone 317-925-2200
Email csprings@iupui.edu
Status Recruiting
Phase Phase 2
Start date May 4, 2020
Completion date September 1, 2030

See also
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