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 @ 11:14 PM
Ignite Modification Date:
2025-12-25 @ 8:49 PM
NCT ID:
NCT01652469
Group ID:
EG001
Title:
B: Docetaxel
Description:
Docetaxel in standard dose. Until progression (clinical or radiological) or unacceptable toxicity.
Docetaxel: Docetaxel 75 mg/m2 as an IV infusion every 21 days.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
41
Other Number Affected:
39
Other Number At Risk:
41
Study:
NCT01652469
Results Section:
NCT01652469
Adverse Events Module:
NCT01652469