- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01196325
Anterior and Posterior Segment Vascular Changes Following Laser and Anti-Vascular Endothelial Growth Factor (VEGF) Treatment of Diabetic Retinopathy (VEGF)
Anterior and Posterior Segment Vascular Changes Following Laser and Anti-Vascular Endothelial Growth Factor (VEGF) Treatment of Diabetic Retinopathy.
Study Overview
Status
Conditions
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
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Ontario
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Toronto, Ontario, Canada, M5T2S8
- Recruiting
- Toronto Western Hospital
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Contact:
- Olena Puzyeyeva, MD
- Phone Number: (416)603-5694
- Email: opuzyeye@uhnresearch.ca
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Contact:
- Lee-Anne Khuu, MSc
- Phone Number: (416)603-5694
- Email: lkhuu@uhnresearch.ca
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Sub-Investigator:
- John G Flanagan, PhD
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Sub-Investigator:
- Efrem Mandelcorn, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Laser Group
Patients who are clinically indicated for the laser treatment
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Anti-VEGF Group (Bevacizumab)
Patients who are clinically indicated for the intravitreal injection of Bevacizumab
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Anti-VEGF Group (Ranibizumab)
Patients who are clinically indicated for intravitreal injection of Ranibizumab
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Age-matched controls
Group of non-diabetic participants who will be age and gender matched
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Quantitative inner retinal blood flow
Time Frame: Baseline, 3, 7, 30 days and 3 months
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Inner retinal blood flow will be measured using Canon Laser Blood Flowmeter
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Baseline, 3, 7, 30 days and 3 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Mean retinal thickness for an annulus centered on fovea
Time Frame: Baseline,3,7,30 days, and 3 months
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Mean retinal thickness will be measured using Heidelberg Spectralis Spectral Domain Optical Coherence Tomography
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Baseline,3,7,30 days, and 3 months
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Best Corrected Visual Acuity (LogMAR, EDTRS)
Time Frame: Baseline, 3, 7, 30 days and 3 months
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Best Corrected Visual Acuity will be examined using 96% and 10 % contrast EDTRS letter charts.
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Baseline, 3, 7, 30 days and 3 months
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Quantitative anterior blood flow
Time Frame: Baseline, 3, 7, 30 days and 3 months
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Quantitative anterior blood flow will be assessed by measuring velocity of individual rbc's (μm/sec) and blood oxygen saturation(%)
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Baseline, 3, 7, 30 days and 3 months
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Mean angle opening distance and trabecular-iris spur area
Time Frame: Baseline, 3, 7, 30 days and 3 months
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Mean angle opening distance and trabecular-iris spur area will be measured by Heidelberg Slit-Lamp Optical Coherence Tomography.
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Baseline, 3, 7, 30 days and 3 months
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09-0258-BE
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.
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