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 @ 12:18 AM
Ignite Modification Date:
2025-12-25 @ 10:21 PM
NCT ID:
NCT04037358
Group ID:
EG000
Title:
Radium-223 and SABR
Description:
First radium-223 infusion will be within two weeks of SABR
Radium-223: Radium-223 plus SABR will be within two weeks.
stereotactic ablative radiotherapy (SABR): SABR 1-5 fractions
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
31
Other Number Affected:
30
Other Number At Risk:
31
Study:
NCT04037358
Results Section:
NCT04037358
Adverse Events Module:
NCT04037358