Clinical Trials Directory

Trials / Completed

CompletedNCT04641234

A Study Reviewing Medical Records to Learn More About Treat-and-extend With Eylea in Patients With Neovascular Age-related Macular Degeneration (nAMD).

Belgian Retrospective Chart Review Evaluating Treat-and-extend With Eylea® in Treatment naïve Patients With Neovascular Age-related Macular Degeneration.

Status
Completed
Phase
Study type
Observational
Enrollment
330 (actual)
Sponsor
Bayer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In people with neovascular age-related macular degeneration (nAMD), the body makes too much of a protein called vascular endothelial growth factor (VEGF). This causes too many blood vessels to grow in a part of the eye called the macula. These blood vessels can damage the macula, causing dark spots and blurriness in central vision. The study drug, aflibercept, works by reducing VEGF levels in the eye.It has already been approved for patients to receive as a treatment for nAMD in a fixed 8-weekly or treat-and-extend dosing regimen after having received 3 monthly doses at the start of treatment. In this study, the researchers want to learn more about how often patients received aflibercept and how their vision changed. The study will include patients with nAMD who had not received treatment to reduce VEGF levels in the eye before. These patients will have started treatment with aflibercept between January 2016 and November 2018. The study will include about 330 men and women who are at least 18 years old. All of the patients had received aflibercept eye injections based on their doctor's instructions. The researchers will use the patients' medical records from January 2016 to November 2020 to measure the following: * the number of aflibercept eye injections the patients received * how long the patients could wait between treatments * the change in the patients' vision * how many patients stopped treatment and why. * associations between patient and disease characteristics at the start of treatment with the number of aflibercept injections and patient's vision during treatment.

Conditions

Interventions

TypeNameDescription
DRUGAflibercept (Eylea, VEGF Trap-Eye, BAY86-5321)As prescribed by the treating physician

Timeline

Start date
2020-12-11
Primary completion
2021-06-09
Completion
2021-06-09
First posted
2020-11-23
Last updated
2022-06-10

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04641234. Inclusion in this directory is not an endorsement.