Purpose: To evaluate the efficacy of intravitreal bevacizumab (IVB) on focal edema with hard exudates secondary to diabetic retinopathy. Design: Prospective interventional case series. Participants: Ten eyes of 10 consecutive patients showing focal edema with hard exudates secondary to diabetic retinopathy which are not eligible for focal laser photocoagulation due to central location (\< 500 µm from fovea).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Bevacizumab (1.25 mg in 0.05 ml) (Avastin; Genentech Inc., San Francisco, CA, USA)
Seoul St Mary's hospital
Seocho, Seoul, South Korea
RECRUITINGChanges in best-corrected visual acuity (BCVA)
ETDRS BCVA will be measured after 6 6 serial IVB.
Time frame: from month 0 to month 6 in monthly schedule (upto 6 months)
amount of hard exudates detected on fundus photography
on fundus photography
Time frame: from month 0 to month 6 in bimonthly schedule (upto 6 months)
macular edema detected by optical coherent tomography
central subfield thickness will be measured.
Time frame: from month 0 to month 6 in bimonthly schedule (upto 6 months)
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