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 @ 12:25 PM
Ignite Modification Date:
2025-12-25 @ 12:04 PM
NCT ID:
NCT01251861
Group ID:
EG000
Title:
Arm A (Observation + Bicalutamide)
Description:
Patients undergo observation on weeks 1-12. Patients then receive bicalutamide PO QD on weeks 13-44. Patients with a PSA decline of \>= 50% may continue on bicalutamide until week 72 in the absence of disease progression or unacceptable toxicity.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
50
Other Number Affected:
39
Other Number At Risk:
50
Study:
NCT01251861
Results Section:
NCT01251861
Adverse Events Module:
NCT01251861