Clinical Trials Directory

Trials / Completed

CompletedNCT06416241

Intravitreal Aflibercept for Macular Edema Due to Central Retinal Vein Occlusion

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
51 (actual)
Sponsor
University of Athens · Academic / Other
Sex
All
Age
18 Years – 95 Years
Healthy volunteers
Accepted

Summary

Central retinal vein occlusion (CRVO) is a common retinal vascular disorder, occurring when there is a blockage to the main blood vessel that transports blood away from the retina. CRVO may cause visual impairment, especially due to macular edema (swelling of the macula due to fluid accumulation) and macular non-perfusion. Aflibercept has been found to improve visual acuity and reduce macular thickness in pivotal trials. The purpose of this study was to evaluate the efficacy and safety of intravitreal aflibercept in real-world, using a patient-fitted treatment regimen. Additionally, imaging parameters have been assessed before and after treatment with intravitreal aflibercept.

Conditions

Interventions

TypeNameDescription
DRUGEYLEA 2 MG in 0.05 ML InjectionIntravitreal injection

Timeline

Start date
2017-01-01
Primary completion
2020-12-31
Completion
2024-03-31
First posted
2024-05-16
Last updated
2024-05-16

Regulatory

Source: ClinicalTrials.gov record NCT06416241. Inclusion in this directory is not an endorsement.