Diabetic Macular Edema Clinical Trial
Official title:
Intravitreal Bevacizumab and Intravitreal Triamcinolone Associated to Laser Photocoagulation for Diabetic Macular Edema(IBeTA)
Intravitreal triamcinolone has been effective for central macular thickness reduction and concomitant visual acuity improvement in patients with diabetic macular edema (DME). VEGF is a very effective inducer of permeability, being 50.000 times more potent than histamine, and may exert its effect on retinal vascular permeability by altering tight-junctions proteins, such as occluding and VE-cadherin. Based on these principles, there is a rationale for anti-VEGF agents treatment of increased retinal capillary permeability conditions, such as diabetic macular edema. Therefore, the purpose of this study is to evaluate the effects of intravitreal bevacizumab and intravitreal triamcinolone associated to laser photocoagulation for diabetic macular edema.
Macular edema is a leading cause of decreased visual acuity in patients with diabetic
retinopathy1,2.
Laser photocoagulation is the standard of care treatment for diabetic macular edema, based
on ETDRS and recent clinical trials findings3,4. However, because visual acuity improvement
post-laser is observed infrequently, and because of the frequent recurrence or persistence
of DME (refractory DME) after appropriate laser treatment, particularly in eyes presenting
with angiographically diffuse macular edema5-9, there is a need for alternative treatments
for the management of DME. In addition, for some patients with significant cataract, precise
visualization of posterior pole structures may not be possible, so that pharmacological
therapy with intravitreal agents may be preferable over laser treatment.
Recent studies have shown promising results of pharmacological therapies for Diabetic
macular edema. Triamcinolone has shown similar results when compared to ranibizumab and
deferred focal/grid LASER in pseudophakic eyes (DRCRnet, prompt versus deferred).
Ranibizumab associated with deferred LASER or as monotherapy has also shown promising
results (RISE and RIDE). However, there are several concerns regarding long-term
intravitreal injections therapies that include economic feasibility for the public health
system, risk of endophthalmitis and patient acceptability. For these reasons, the present
study decided to check associations between LASER and drug therapy, in an attempt to improve
focal/grid laser outcomes with reduced number of intravitreal injections.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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