Changes to the Retina Following Anti-VEGF Treatments for Diabetic Macular Edema

Sponsor
Lawson Health Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT02979665
Collaborator
(none)
51
35

Study Details

Study Description

Brief Summary

anti-VEGF therapy is an established method to control leakage and abnormal growth of retinal blood vessels. Questions on the long-term effect on the retina, intraocular pressure and on the overall retinal perfusion from these treatments remain to be answered. The purpose of the study was to evaluate changes in the retina following anti-VEGF treatment over time, using structural and functional diagnostic tests.

Condition or Disease Intervention/Treatment Phase
  • Drug: Ranibizumab Ophthalmic

Detailed Description

Diabetic retinopathy (DR) causes changes in the capillaries that nourish the retina. Two treatments clinically used for DR are laser photocoagulation to reduce the angiogenic drive by knocking off metabolically active retina and anti-VEGF drugs for diabetic macular edema (DME). DME affects approximately 2.5% of the nearly 2.4 million Canadians with diabetes, or approximately 60,000 Canadians, making it a major cause of adult-onset vision loss. DME occurs when blood vessels in the retina of diabetic patients become leaky resulting in unwanted fluid accumulation in the center of vision known as the macula. If not treated, this can lead to blindness. Originally used in the treatment of age-related macular degeneration (AMD), anti-VEGF drugs are increasingly used to control leakage and abnormal growth of retinal blood vessels. Numerous questions have emerged following the usage of anti-VEGF medications in the eye such as their long-term effects of these drugs on intraocular pressure and on the overall retinal perfusion. By recruiting DR patients requiring anti-VEGF treatment for DME, this study will answer whether long-term usage of anti-VEGF will result in structural and functional changes to the retina.

Study Design

Study Type:
Observational
Actual Enrollment :
51 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Clinico-Pathological Study of the Structural and Functional Changes to the Retina Following Anti-VEGF Treatments for Diabetic Macular Edema
Study Start Date :
Sep 1, 2014
Actual Primary Completion Date :
Aug 1, 2017
Actual Study Completion Date :
Aug 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Ranibizumab Ophthalmic

DME consults requiring anti-VEGF treatment

Drug: Ranibizumab Ophthalmic
Ranibizumab (trade name Lucentis among others) is a monoclonal antibody fragment (Fab) created from the same parent mouse antibody as bevacizumab. It is an anti-angiogenic that has been approved to treat the "wet" type of age-related macular degeneration (AMD, also ARMD), a common form of age-related vision loss and diabetic macular edema (DME).
Other Names:
  • Lucentis
  • Control

    DME consults not requiring anti-VEGF

    Outcome Measures

    Primary Outcome Measures

    1. Effects of anti-VEGF drugs on intraocular pressure (mmHg) [2 year]

    Secondary Outcome Measures

    1. Effects of anti-VEGF drugs on macular thickness (um) [2 year]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • DME patients

    • Require anti-VEGF injections in at least one eye

    Exclusion Criteria:
    • Advanced lens opacity or cataract that could affect diagnostic testing

    • Prior retinal treatment (PRP, focal laser or surgery within 6 months of participation)

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Lawson Health Research Institute

    Investigators

    • Principal Investigator: Cindy Hutnik, MD, PhD, St. Joseph's Health Care London

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Lawson Health Research Institute
    ClinicalTrials.gov Identifier:
    NCT02979665
    Other Study ID Numbers:
    • 105570
    First Posted:
    Dec 1, 2016
    Last Update Posted:
    May 2, 2019
    Last Verified:
    Apr 1, 2019
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 2, 2019