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 @ 12:27 AM
Ignite Modification Date:
2025-12-25 @ 10:32 PM
NCT ID:
NCT01342367
Group ID:
EG001
Title:
Oral ADT Group
Description:
Combined androgen blockade in the oral ADT group was bicalutamide 50 mg daily with an oral 5-AR inhibitor (i.e. finasteride 5 mg, or dutasteride 0.5 mg daily), fo rtotal duration of 2 year sand 4 months Bicalutamide given for 4 months RT given 6 8 weeks
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
40
Other Number Affected:
18
Other Number At Risk:
40
Study:
NCT01342367
Results Section:
NCT01342367
Adverse Events Module:
NCT01342367