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 @ 2:01 AM
Ignite Modification Date:
2025-12-26 @ 12:25 AM
NCT ID:
NCT02312960
Group ID:
EG000
Title:
From Study 15396 Radium-223 Dichloride+Abi/Pred Group
Description:
Safety FU from feeder study 15396. Participants received radium-223 dichloride 50 kBg/kg (55 kBq/kg after implementation of National Institute of Standards and Technology \[NIST\] update) at intervals of every 4 weeks, along with abiraterone acetate plus prednisone/prednisolone (abi/pred) for up to 6 cycles.
Deaths Number Affected:
24
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
39
Other Number Affected:
2
Other Number At Risk:
39
Study:
NCT02312960
Results Section:
NCT02312960
Adverse Events Module:
NCT02312960