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 @ 3:19 AM
Ignite Modification Date:
2025-12-26 @ 1:58 AM
NCT ID:
NCT04740905
Group ID:
EG001
Title:
Arm B: Aflibercept Q4W (Part 1)
Description:
In Part 1 (Day 1 through Week 24), participants randomly assigned to Arm B were to receive aflibercept 2 milligrams (mg) administered by intravitreal (IVT) injection once every 4 weeks (Q4W) from Day 1 through Week 20 (a total of 6 injections).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
274
Other Number Affected:
69
Other Number At Risk:
274
Study:
NCT04740905
Results Section:
NCT04740905
Adverse Events Module:
NCT04740905