Corneal Crosslinking for Treatment of Corneal Neovascularization

  • days left to enroll
  • participants needed
  • sponsor
    Price Vision Group
Updated on 4 October 2022


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.

Condition Corneal Neovascularization
Treatment 30 minute photoactivation of riboflavin 0.1%, 10 minute photoactivation of riboflavin 0.1%
Clinical Study IdentifierNCT04787471
SponsorPrice Vision Group
Last Modified on4 October 2022


Yes No Not Sure

Inclusion Criteria

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 Criteria

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
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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