Retinal Blood Flow and Microthrombi in Type 1 Diabetes
The project aims to find mechanisms for the abnormal retinal blood flow that in diabetic patients often precedes any evidence of clinical retinopathy and may contribute to the development of retinopathy.
Specifically, the projects tests the hypothesis that reduced retinal blood flow found in young patients with type 1 diabetes reflects increased resistance in the small vessels of the retina caused by the formation of small blood clots, called microthrombi; and that antiplatelet agents normalize the reduced retinal blood flow.
Description
The ultimate goal of this research is to contribute to the development of strategies to prevent diabetic retinopathy. This project will test the hypothesis that antiplatelet agents normalize the reduced blood flow observed early in the course of type 1 diabetes. If the hypothesis is proven correct, the results will indicate that the formation of small blood clots (microthrombi) occurs early in diabetic retinal vessels. In turn, because microthrombosis could readily account for the occlusive microangiopathy that causes the sight-threatening stages of diabetic retinopathy, the results will propose the desirability of antiplatelet therapy for the prevention of diabetic retinopathy.
We have three specific aims:
To confirm that, under basal conditions, retinal blood flow measured with the laser Doppler method in a group of type 1 diabetic patients with no or minimal retinopathy differs from the flow measured in age- and sex-matched nondiabetic control subjects;
To determine whether the response of retinal blood flow to low-dose aspirin (81 mg/day) administered for 2 months versus placebo, differs between type 1 diabetic patients with no or minimal retinopathy and age- and sex-matched nondiabetic control subjects;
To determine whether in type 1 diabetic patients with no or minimal retinopathy the response of retinal blood flow to low-dose aspirin differs from the response to clopidogrel, a drug that interferes with platelet function downstream of the site of aspirin action.
Status: Completed (Phase 2). Started on June 1st, 2003. Ended on March 1st, 2006.
Enrollment: 100 subjects
Study Type: Interventional
Study Design:
- Diagnostic
- Randomized
- Double-Blind
- Placebo Control
- Parallel Assignment
- Efficacy Study
Conditions:
Interventions:
- Drug: aspirin
- Drug: clopidogrel
Eligibility
Inclusion Criteria:
Age 18-45 years,
type 1 diabetes duration 1-15 years,
absent or minimal retinopathy (EDTRS 20).
Age- and gender-matched healthy controls
Exclusion Criteria:
systemic diseases other than diabetes,
retinal diseases other than diabetic retinopathy,
bleeding disorders,
aspirin allergy,
use of anti-platelet agents,
non-steroidal anti-inflammatory agents,
angiotensin converting enzyme inhibitors,
angiotensin receptor antagonists,
Vitamin E in large doses.
- Gender
Both
- Mininum Age
18 Years
- Maximum Age
45 Years
- Healthy Volunteers
Accepts Healthy Volunteers
Resources
Source: Schepens Eye Research Institute
Authority: United States: Food and Drug Administration
Locations
-
Schepens Eye Research Institute
Boston
Massachusetts
02114
United States
Officials
Mara Lorenzi, MD (Principal Investigator, Schepens Eye Research Institute)
Sponsors
Schepens Eye Research Institute (Lead Sponsor)
References
None.
Links
None.
- Date Verified
- March 1st, 2006
- First Received
- December 1st, 2006
- Last Changed
- December 1st, 2006
Information obtained from ClinicalTrials.gov on July 15, 2008. Link to the current ClinicalTrials.gov record.
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