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Aflibercept for Diabetic Macular Edema In Real-life Practice in GREece (ADMIRE)

N

National and Kapodistrian University of Athens

Status

Completed

Conditions

Diabetic Macular Edema

Treatments

Drug: Aflibercept

Study type

Observational

Funder types

Other

Identifiers

NCT05683912
698/2019

Details and patient eligibility

About

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.

Enrollment

100 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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