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 @ 3:04 AM
Ignite Modification Date:
2025-12-26 @ 1:43 AM
NCT ID:
NCT04493333
Group ID:
EG000
Title:
Intrarosa & Standard of Care Aromatase Inhibitor
Description:
Subjects randomized to the Intrarosa® arm will use 6.5 mg daily for 12 weeks (±1 week).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
5
Other Number Affected:
4
Other Number At Risk:
5
Study:
NCT04493333
Results Section:
NCT04493333
Adverse Events Module:
NCT04493333