RecruitingPhase 2Phase 3NCT04787471

Corneal Crosslinking for Treatment of Corneal Neovascularization

Randomized Comparison of Standard vs. Accelerated Corneal Crosslinking for Treatment of Corneal Neovascularization With or Without Concomitant Inflammation and/or Infection


Sponsor

Price Vision Group

Enrollment

62 participants

Start Date

May 3, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

The study objective is to assess safety and efficacy of photo-activation of riboflavin for treatment of corneal neovascularization with or without concomitant inflammation and/or infection.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • years of age or older
  • With active inflammation or infection causing vascularization and possibly melting of the cornea, or vessels extending into the cornea causing lipid deposition, or vascularization that could significantly increase the risk of rejection of a current or planned corneal transplant, or vessels that continue to extend into the cornea despite topical treatment with corticosteroids.
  • Signed written informed consent.

Exclusion Criteria3

  • Known sensitivity to treatment medications
  • Current condition that in the investigator's opinion could compromise safety or data integrity.
  • Pregnancy (including plan to become pregnant) or lactation during the course of the study

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Interventions

COMBINATION_PRODUCT30 minute photoactivation of riboflavin 0.1%

Use of riboflavin 0.1% eye drops and 3mW/cm2 UVA light for 30 minutes

COMBINATION_PRODUCT10 minute photoactivation of riboflavin 0.1%

Use of riboflavin 0.1% eye drops and 9mW/cm2 UVA light for 10 minutes


Locations(1)

Price Vision Group

Indianapolis, Indiana, United States

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NCT04787471


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