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:
EG002
Title:
Arm C (Bevacizumab and Sorafenib)
Description:
Patients receive bevacizumab 5 mg/kg IV over 30-90 minutes on days 1 and 15 and sorafenib 200 mg PO BID on days 1-5, 8-12, 15-19, and 22-26 in a 28-day cycle.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
74
Serious Number At Risk:
90
Other Number Affected:
89
Other Number At Risk:
90
Study:
NCT00378703
Results Section:
NCT00378703
Adverse Events Module:
NCT00378703