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 @ 7:33 PM
Ignite Modification Date:
2025-12-25 @ 5:15 PM
NCT ID:
NCT00378703
Group ID:
EG001
Title:
Arm B (Bevacizumab and Temsirolimus)
Description:
Patients receive temsirolimus 25 mg IV over 30 minutes on days 1, 8, 15, and 22 and bevacizumab as in Arm A in a 28-day cycle.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
66
Serious Number At Risk:
86
Other Number Affected:
86
Other Number At Risk:
86
Study:
NCT00378703
Results Section:
NCT00378703
Adverse Events Module:
NCT00378703