Photodynamic Therapy With Verteporfin for Corneal Neovascularization

Sponsor
Chonnam National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00471406
Collaborator
(none)

Study Details

Study Description

Brief Summary

Purpose: To investigate the efficacy of photodynamic therapy with verteporfin for the treatment of patients with corneal neovascularization.

Design: Prospective, non-comparative case series. Participants: Eighteen eyes of 18 patients with stable corneal neovascularization who were refractory to conventional treatment.

Methods: The patients were treated with photodynamic therapy with verteporfin (6 mg/m2). Five patients were treated following penetrating keratoplasty, and 2 patients were treated before penetrating keratoplasty. Best corrected visual acuity and anterior segment photography were performed before and after treatment. The length of cumulative blood vessels and area of corneal neovascularization were measured.

Main outcome measures: Vascular occlusion, best corrected visual acuity, cumulative blood vessel length, and corneal neovascularization area.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Photodynamic Therapy with Verteporfin
N/A

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    35 Years to 70 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Patients with clinically stable corneal neovascularization who were not improved after treatment with 1% prednisolone acetate eyedrops instilled 4 times a day for at least 1 month
    Exclusion Criteria:
    • Individuals who had active keratitis with vessel proliferation, uncontrolled inflammation, active hepatitis or clinically significant liver disease, or porphyria or other porphyrin sensitivity

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Chonnam National University Hospital

    Investigators

    • Study Director: Kyung chul Yoon, MD, Chonnam natianl university hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00471406
    Other Study ID Numbers:
    • CPDT-0001
    First Posted:
    May 9, 2007
    Last Update Posted:
    Oct 17, 2008
    Last Verified:
    Oct 1, 2008

    Study Results

    No Results Posted as of Oct 17, 2008