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ADMIRE was a prospective, observational cohort study of patients with diabetic macular edema (DME). Efficacy was assessed by change in best-corrected visual acuity (BCVA) and central retinal thickness (CRT) from baseline to months 12, 24 and 36 after treatment with intravitreal aflibercept in treatment-naïve patients and previously treated patients. Safety was evaluated by recording any patients-reported events.
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Inclusion criteria
Patients with DM, able to give written informed consent Patients with DME>320 μm, who need treatment
Exclusion criteria
Patients with other retinal diseases than DME Intraocular surgery within the last 6 months
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Data sourced from clinicaltrials.gov
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