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:
2025-12-25 @ 12:13 AM
Ignite Modification Date:
2025-12-25 @ 10:14 PM
NCT ID:
NCT02596958
Group ID:
EG000
Title:
Bevacizumab
Description:
Participants received bevacizumab (Avastin) in addition to platinum based chemotherapy for up to 6 cycles (21-day cycles) followed by bevacizumab as a single agent until disease progression. The dose and administration schedule was at the discretion of the treating physician and as per the recommendations given in the current SmPC.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
110
Serious Number At Risk:
987
Other Number Affected:
851
Other Number At Risk:
987
Study:
NCT02596958
Results Section:
NCT02596958
Adverse Events Module:
NCT02596958