Eylea Safety and Effectiveness for Neovascular Glaucoma
This study aims to observe the safety and effectiveness of Eylea in individuals with neovascular glaucoma by monitoring for adverse events.
Data Collection
Collected from today forward - ProspectiveEye Diseases+1
+ Glaucoma
+ Ocular Hypertension
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: November 27, 2020
Actual date on which the first participant was enrolled.This study is focused on understanding how safe and effective the drug Eylea is for treating Neovascular Glaucoma, a serious eye condition that can lead to vision loss. The study involves patients who have already been diagnosed with this condition and whose doctors have chosen Eylea as part of their treatment plan. The main goal is to gather real-world information about how patients respond to Eylea over time, which can help improve future treatment options and care for those affected by this type of glaucoma. Participants in the study will receive Eylea as part of their regular treatment and will be monitored for six months. During this time, researchers will collect detailed information at the start, during regular follow-up visits, and at the end of the study. The primary focus is on recording any adverse events, which are any unexpected problems or side effects that occur during treatment. This information is crucial for determining how safe Eylea is for patients in everyday clinical settings.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.480 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location