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 @ 6:51 PM
Ignite Modification Date:
2025-12-25 @ 4:23 PM
NCT ID:
NCT00796757
Group ID:
EG000
Title:
Bevacizumab + Interferon
Description:
Participants received bevacizumab 5 mg/kg IV on Day 1 and IFN 3 MIU SC 3 times per week with at least 1 day between injections. This cycle lasted for 2 weeks and was repeated until disease progression, unacceptable toxicity, or participant withdrawal.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
146
Other Number Affected:
113
Other Number At Risk:
146
Study:
NCT00796757
Results Section:
NCT00796757
Adverse Events Module:
NCT00796757