Studies | Similarities | Differences |
---|---|---|
BRVO | Â | Â |
Design: double-blind | Patients failing to achieve sufficient improvement in BCVA could receive laser in BRAVO | |
Date of study | Duration of macular oedema before study commencement: 3.3–3.7 months vs. 5.1–5.3 months across treatment groups for BRAVO and GENEVA, respectively | |
Duration of follow-up: | ||
6Â months | ||
Size | ||
Patient demographics | ||
Design: double-blind | Patients failing to achieve sufficient improvement in BCVA could receive laser therapy in BRAVO | |
Date of study | Size: 81 patients (Moradian) vs. 397 patients (BRAVO) | |
Patient age: 58 years (Moradian) vs. 66 years (BRAVO) | ||
Duration of macular oedema at baseline: 6 weeks (Moradian) vs. 3.5Â months (BRAVO) | ||
Duration of follow-up: 3 months (Moradian) vs. 6 months (BRAVO) | ||
BCVA endpoint: change in logMAR reported for Moradian | ||
Patient demographics | Patients failing to achieve sufficient improvement in BCVA could receive laser therapy in BRAVO | |
Size | Design: double-blinded for BRAVO but single-blinded for BVOS (patients were aware of their treatment) | |
Duration of follow-up: 6 months vs. 36 months | ||
Patient demographics | Patients failing to achieve sufficient improvement in BCVA could receive laser in BRAVO | |
Size: 77 patients (Battaglia Parodi) vs. 397 patients (BRAVO) | ||
Design: blinded for BRAVO but not reported for Battaglia Parodi | ||
Duration of follow-up: 24 months (Battaglia Parodi) vs. 6 months (BRAVO) | ||
Duration of BRVO: < 15 days for Battaglia Parodi vs. < 12 months for BRAVO (inclusion criterion) | ||
CRVO | Â | Â |
Design: double-blind | Duration of macular oedema before study commencement: 2.9–3.6 months vs. 5.1–5.3 months across treatment groups for CRUISE and GENEVA, respectively | |
Date of study | ||
Duration of follow-up: 6 months | Baseline BCVA: 47.4–49.2 letters vs. 53.9–54.8 letters across treatment groups for CRUISE and GENEVA, respectively | |
Size | ||
Patient demographics | ||
Size | Design: blinded for CRUISE but single-blinded for CVOS (patients were aware of their treatment) | |
Patient demographics | Duration of macular oedema at baseline: > 3 months for CVOS, < 12 months for CRUISE (inclusion criteria) | |
Duration of follow-up: 36 months (CVOS) vs. 6 months (CRUISE) | ||
Patient demographics | Size: 48 patients (Laatikainen) vs. 392 patients (CRUISE) | |
Design: blinded for CRUISE but not Laatikainen | ||
Duration of follow-up: 12 months (Laatikainen) vs. 6 months (CRUISE) | ||
Duration of macular oedema at baseline: < 3 months for Laatikainen vs. < 12 months for CRUISE (inclusion criterion) | ||
Patient demographics | Size: 34 patients (May) vs. 392 patients (CRUISE) | |
Design: blinded for CRUISE but not May | ||
Duration of follow-up: 24 months (May) vs. 6 months (CRUISE) | ||
CRVO duration at baseline: not specified for May vs. < 12 months for CRUISE (inclusion criterion) |