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:
EG007
Title:
All Aflibercept HD (Week 0- 156)
Description:
All participants from aflibercept HDq12 (Week 0-156) and aflibercept HDq16 (Week 0-156). Participants in this group could have their treatment intervals adjusted in the extension according to pre-specified dose regimen modification (E-DRM) criteria.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
122
Serious Number At Risk:
417
Other Number Affected:
255
Other Number At Risk:
417
Study:
NCT04423718
Results Section:
NCT04423718
Adverse Events Module:
NCT04423718