Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-25 @ 1:23 AM
Ignite Modification Date:
2025-12-25 @ 11:32 PM
NCT ID:
NCT03622593
Group ID:
EG002
Title:
C: Aflibercept 2 mg Q8W
Description:
Participants randomized to Arm C received 2 milligrams (mg) aflibercept intravitreal (IVT) injections Q4W to Week 16, followed by 2 mg aflibercept IVT injections Q8W to Week 96, followed by the final study visit at Week 100.
Deaths Number Affected:
10
Deaths Number At Risk:
None
Serious Number Affected:
100
Serious Number At Risk:
314
Other Number Affected:
178
Other Number At Risk:
314
Study:
NCT03622593
Results Section:
NCT03622593
Adverse Events Module:
NCT03622593