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 @ 5:05 AM
Ignite Modification Date:
2025-12-26 @ 4:07 AM
NCT ID:
NCT04423718
Group ID:
EG002
Title:
Aflibercept HDq16 (Week 0- 96)
Description:
Participants enrolled in main study received high dose (HD) aflibercept administered every 16 weeks after 3 initial injections at 4-week intervals. Participants in this group could have their treatment intervals adjusted according to pre-specified dose regimen modification (DRM) criteria.
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
72
Serious Number At Risk:
338
Other Number Affected:
180
Other Number At Risk:
338
Study:
NCT04423718
Results Section:
NCT04423718
Adverse Events Module:
NCT04423718