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:
NCT01681433
Group ID:
EG001
Title:
Control Arm: Arm B
Description:
Continuation of standard therapy with abiraterone acetate and prednisone
Abiraterone Acetate: Standard therapy: Abiraterone Acetate 1000 mg PO daily
Prednisone: Standard therapy: Prednisone 10-20 mg PO daily
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
36
Other Number Affected:
32
Other Number At Risk:
36
Study:
NCT01681433
Results Section:
NCT01681433
Adverse Events Module:
NCT01681433