The primary objective of this study is to evaluate if a combination therapy with micropulse diode laser treatment shows non inferiority on visual acuity within 12 months in comparison to standard therapy (intravitreal injection of ranibizumab only).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Klinik für Augenheilkunde, Klinikum Chemnitz gGmbH
Chemnitz, Germany
change in best corrected visual acuity (BCVA)
Time frame: baseline, 12 month
change in central macular thickness
Time frame: baseline, 12 month
number of intravitreal Lucentis injections
Time frame: within 12 month
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