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:
2025-12-24 @ 12:16 PM
Ignite Modification Date:
2025-12-25 @ 12:01 PM
NCT ID:
NCT01023061
Group ID:
EG000
Title:
Treatment (Antihormone Therapy and Radiation Therapy)
Description:
Patients receive abiraterone acetate and prednisone for 24 weeks. Patients also receive leuprolide acetate or goserelin in weeks 1 and 13. Patients undergo external beam radiotherapy starting in week 15 for 8.5 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity.
abiraterone acetate: Given orally
prednisone: Given orally
leuprolide acetate: Given via injection
laboratory biomarker analysis: Correlative study
external beam radiation therapy: Undergo radiotherapy
goserelin acetate: Given via injection
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
22
Other Number Affected:
19
Other Number At Risk:
22
Study:
NCT01023061
Results Section:
NCT01023061
Adverse Events Module:
NCT01023061