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Clinical Trial Summary

To determine whether the Peschke PXL-330 system 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 NCT03918408
Study type Interventional
Source Pacific Clear Vision Institute
Contact BALAMURALI AMBATI, MD, PhD
Phone 541-343-5000
Email bambati@pcvi.com
Status Recruiting
Phase Phase 1
Start date September 1, 2019
Completion date June 2030

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