Anterior and Posterior Segment Vascular Changes Following Laser and Anti-Vascular Endothelial Growth Factor (VEGF) Treatment of Diabetic Retinopathy (VEGF)

January 23, 2013 updated by: Chris Hudson, University of Toronto

Anterior and Posterior Segment Vascular Changes Following Laser and Anti-Vascular Endothelial Growth Factor (VEGF) Treatment of Diabetic Retinopathy.

The study will investigate changes in the structure and function of blood vessels in the front and back of the eye following laser and anti-VEGF treatments for sight-threatening diabetic eye disease. Sixty four volunteers will be recruited, including age-matched control subjects and diabetic patients who require conventional or contemporary treatment for pre-existing diabetic eye disease. Volunteers will be assessed before and after treatment using state-of-the-art techniques to measure vision, the rate of blood flow and structure at the front and back of the eye and the effectiveness of blood flow delivery. Changes following treatment in these novel, non-invasive techniques will be quantified and described. We anticipate that conventional and new / developing treatments will lead to narrowing of the vessels and consequent reduction of blood flow at the back and front of the eye. There will be a strong relationship between structural changes of the eye and functional changes of blood vessels at the front and back of the eye. The results of this study will improve our understanding of the impact of the various treatments on the entire eye. The research will also ensure an improved understanding of the mechanisms of action of the various treatments and will provide insight of reasons for good or poor outcomes, based upon specific changes in structure and blood flow.

Study Overview

Status

Unknown

Detailed Description

Diabetic Retinopathy (DR) is the single leading cause of blindness in people of working age. The total number of people living with diabetes in Canada is well over 2 million. The WHO estimates that around 12% of people with diabetes are blind or will develop severe vision loss. The two most common treatments of DR are: Laser Photocoagulation and anti-VEGF intravitreal injection. Clinical evidence demonstrates that these treatments lead to morphological and vascular retinal changes, however the actual mechanism and nature of post treatment changes is not fully understood. It is only recently that objective and quantitative imaging and hemodynamic technologies with previously unachievable resolution have become available that enable us to evaluate and to compare various effects of these treatments on vital eye structures.

We are proposing to take advantage of these state-of-the-art technologies in order to explore unknown effects of treatments on vital eye structures. We hypothesize that: 1) Laser Photocoagulation and anti-VEGF treatments will result in vessel constriction and hence reduction in posterior (retinal and choroidal) and anterior (conjunctival) ocular blood flow; 2) Changes in anterior segment ocular morphology and blood flow will positively correlate with changes in posterior segment morphology and blood flow; 3) Combined treatments will result in a greater reduction in posterior and anterior blood flow than any single treatment; 4) There will be differences in anterior and posterior blood flow outcomes and in anterior segment oxygen saturation when compared to healthy controls.

The study will include four groups of participants: Laser treatment group; Intravitreal injection of Bevacizumab treatment group; Intravitreal injection of Ranibizumab treatment group; Healthy age matched controls. The administration of ranibizumab and bevacizumab will be randomized across participants. Randomization number will be assigned to each participant and recorded in a Master Randomization Assignment List. All patients will be recruited from the Retina Clinics of the Toronto Western Hospital.

Every type 2 diabetic patient with Diabetic Macular Edema will be assessed prior to treatment and followed-up on the 3rd, 7th,30th day and 3 months after the initial treatment.

Study Type

Observational

Enrollment (Anticipated)

64

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ontario
      • Toronto, Ontario, Canada, M5T2S8
        • Recruiting
        • Toronto Western Hospital
        • Contact:
        • Contact:
        • Sub-Investigator:
          • John G Flanagan, PhD
        • Sub-Investigator:
          • Efrem Mandelcorn, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

35 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Type 2 diabetic patients with clinically sight-threatening Diabetic Macular Edema will be recruited from the Retina Clinics of Toronto Western Hospital.

Description

Inclusion Criteria:

  • Age range of 35-75 yrs
  • Type 2 diabetes apart from age-matched control group
  • Visual acuity of 20/400 or better
  • Confirmed diagnose of Clinical Significant Diabetic Macular Edema (applies for Diabetic Groups only)
  • Previously untreated eye for retinal diseases and disorders

Exclusion Criteria:

  • Distance refractive error > ± 6.00 DS & / or ± 2.50 DC
  • Intraocular pressure ≥ 22mm Hg
  • Proliferative Diabetic Retinopathy
  • Any other active eye disease and disorder
  • Participants with history of cardiovascular events, stroke, thromboembolic events, transient ischemic attack, uncontrolled hypertension.
  • Any active ocular infection;
  • History of glaucoma;
  • Known allergy, hypersensitivity or contraindication to the study medication;
  • Pregnancy, breast feeding, or women of childbearing potential who are not using a reliable method of contraception;
  • Proteinuria and/or renal impairment;
  • Surgery within the past 28 days.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Laser Group
Patients who are clinically indicated for the laser treatment
Anti-VEGF Group (Bevacizumab)
Patients who are clinically indicated for the intravitreal injection of Bevacizumab
Anti-VEGF Group (Ranibizumab)
Patients who are clinically indicated for intravitreal injection of Ranibizumab
Age-matched controls
Group of non-diabetic participants who will be age and gender matched

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quantitative inner retinal blood flow
Time Frame: Baseline, 3, 7, 30 days and 3 months
Inner retinal blood flow will be measured using Canon Laser Blood Flowmeter
Baseline, 3, 7, 30 days and 3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean retinal thickness for an annulus centered on fovea
Time Frame: Baseline,3,7,30 days, and 3 months
Mean retinal thickness will be measured using Heidelberg Spectralis Spectral Domain Optical Coherence Tomography
Baseline,3,7,30 days, and 3 months
Best Corrected Visual Acuity (LogMAR, EDTRS)
Time Frame: Baseline, 3, 7, 30 days and 3 months
Best Corrected Visual Acuity will be examined using 96% and 10 % contrast EDTRS letter charts.
Baseline, 3, 7, 30 days and 3 months
Quantitative anterior blood flow
Time Frame: Baseline, 3, 7, 30 days and 3 months
Quantitative anterior blood flow will be assessed by measuring velocity of individual rbc's (μm/sec) and blood oxygen saturation(%)
Baseline, 3, 7, 30 days and 3 months
Mean angle opening distance and trabecular-iris spur area
Time Frame: Baseline, 3, 7, 30 days and 3 months
Mean angle opening distance and trabecular-iris spur area will be measured by Heidelberg Slit-Lamp Optical Coherence Tomography.
Baseline, 3, 7, 30 days and 3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2009

Primary Completion (Anticipated)

August 1, 2014

Study Completion (Anticipated)

August 1, 2014

Study Registration Dates

First Submitted

September 3, 2010

First Submitted That Met QC Criteria

September 7, 2010

First Posted (Estimate)

September 8, 2010

Study Record Updates

Last Update Posted (Estimate)

January 24, 2013

Last Update Submitted That Met QC Criteria

January 23, 2013

Last Verified

January 1, 2013

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Diabetic Macular Edema

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