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NCT04787471 · ClinicalTrials.gov registry record · Phase 2

Corneal Crosslinking for Treatment of Corneal Neovascularization

A Phase 2 study of Corneal Neovascularization, sponsored by Price Vision Group.

Recruiting
Registry status
Phase 2
Development phase
62
Enrollment target
1
Study location

NCT04787471: Recruiting Phase 2 study of Corneal Neovascularization, sponsored by Price Vision Group.

NCT04787471 is a Phase 2 study of Corneal Neovascularization that is actively recruiting participants, run by Price Vision Group. The registered enrollment target is 62 participants, roughly in line with the 62-participant average among 3 other Corneal Neovascularization trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04787471, a Phase 2 study of Corneal Neovascularization, is actively recruiting participants, sponsored by Price Vision Group.

RECRUITING
Registry status
Phase 2
Development phase
62 participants
Enrollment target
1
Study location

Study 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.

Primary Outcome

the cornea will be photographed and morphometric image analysis software will be used to measure corneal neovascularization as a proportion of the total corneal area. The proportion measured at baseline will be compared with the proportion measured at 6 months after treatment.

Conditions Studied

Interventions

  • COMBINATION_PRODUCT 30 minute photoactivation of riboflavin 0.1%
  • COMBINATION_PRODUCT 10 minute photoactivation of riboflavin 0.1%

Study Locations (1)

Indiana

  • Price Vision Group - Indianapolis

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2021-05-03
Est. Completion 2026-09-15
Phase Phase 2
Price Vision Group

10 total trials

What NCT04787471 shows while recruiting

NCT04787471 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 62 participants, a relatively small participant target, roughly in line with the 62-participant average among 3 other Corneal Neovascularization trials with a reported enrollment target.

The record links to 1 condition, with Corneal Neovascularization appearing as the primary indexed condition, and to 2 interventions - of which 30 minute photoactivation of riboflavin 0.1% is the first listed.

NCT04787471 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT04787471 about?

NCT04787471 is a clinical study titled "Corneal Crosslinking for Treatment of Corneal Neovascularization". 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.

What is the current status of trial NCT04787471?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 62 participants. The study started on 2021-05-03. Estimated completion is 2026-09-15.

What conditions does trial NCT04787471 study?

This clinical trial studies the following conditions: Corneal Neovascularization.

What interventions are being tested in trial NCT04787471?

The interventions under investigation include: 30 minute photoactivation of riboflavin 0.1% (COMBINATION_PRODUCT), 10 minute photoactivation of riboflavin 0.1% (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT04787471?

This trial is sponsored by Price Vision Group, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04787471 being conducted?

This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT04787471, the US trial registry maintained by the National Library of Medicine. NCT04787471 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.