Clin2
NCT03918408Possibly a fitRecruiting

Platinum eye drops and light to slow keratoconus

Keratoconus, UnstableBacterial KeratitisEctasia of Cornea

Part of Eyes & vision clinical trials.

This Phase 1 study tests whether a specific corneal cross-linking system (called PXL-Platinum 330) is safe and effective for people with progressive keratoconus, a condition that makes the cornea thin and bulge. The goal is to slow vision changes and see how well the treatment works in the short term.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
300 people
Ages
12 years to 45 years
Study type
Interventional

Who can take part

  • Be at least 12 years old
  • Have keratoconus that is getting worse over the last 3+ months (based on exam and tests)
  • Have corneal shape and measurements that match keratoconus, such as steepening in the center/bottom of the cornea and specific topography scan results
  • Have a cornea thickness above a safety cutoff (thinnest point must be 485 microns or more)
  • Be willing and able to come back for follow-up visits
  • Not be pregnant or breastfeeding during the study

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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