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 @ 3:45 AM
Ignite Modification Date:
2025-12-26 @ 2:32 AM
NCT ID:
NCT01637402
Group ID:
EG001
Title:
Dose Escalation
Description:
Dose Escalation (until PSA decrease of at least 30% after 12 weeks):
Abiraterone 1,000 mg, twice daily, Prednisone 5 mg twice daily
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
18
Other Number Affected:
10
Other Number At Risk:
18
Study:
NCT01637402
Results Section:
NCT01637402
Adverse Events Module:
NCT01637402