Proliferative Diabetic Retinopathy Clinical Trial
Official title:
A Pilot Study to Determine if Intravitreal Injections of Pegaptanib Sodium (Macugen) Given Every 12 Weeks for a Year After an Induction Phase of Three Injections Every 6 Weeks Will Reduce the Progression of Proliferative Diabetic Retinopathy in Patients Without Significant Vitreous Hemorrhage in Comparison to Treatment With Retinal Photocoagulation Alone and After an Induction Phase
Intravitreal injections of pegaptanib will induce the regression of Proliferative Diabetic Retinopathy (PDR) and reduce the need for retinal photocoagulation.
Primary Objective:
To further establish the efficacy of intravitreal pegaptanib injections in the regression of
retinal neovascularization secondary to high-risk PDR, as compared to standard panretinal
photocoagulation (PRP)
Secondary Objective:
To maintain the regression of PDR after the induction phase with intravitreal pegaptanib
injections administered at 12-week intervals, as compared to standard PRP
To maintain the regression of PDR after the induction phase with retinal photocoagulation
applied to areas of ischemia (Selective Laser Photocoagulation), as compared to standard PRP
To evaluate the rate of recurrence of neovascularization after 6 intravitreal pegaptanib
injections
To determine if intravitreal pegaptanib will reduce the area and/or volume of concomitant
diabetic macular edema, as assessed by leakage on fluorescein angiography (FA) and/or
optical coherence tomography (OCT)
To determine if intravitreal pegaptanib injections maintain or reduce the loss of
best-corrected visual acuity
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
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