Diabetic Macular Edema Clinical Trial
Eligible eyes are randomized to two groups. Group A will receive three intravitreal
injections of bevacizumab at 4 week intervals. In group B, three intravitreal injections of
combined bevacizumab and fasudil will be performed with the same frequency.
Best corrected visual acuity (BCVA) and central macular thickness (CMT) will be evaluated
prior to injections and then every 4 weeks for 6 months. Fluorescein angiography will be
performed at baseline and at weeks 12 and 24. The two groups will be compared in terms of
BCVA and CMT changes.
n/a
Status | Clinical Trial | Phase | |
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