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 @ 5:01 AM
Ignite Modification Date:
2025-12-26 @ 4:02 AM
NCT ID:
NCT01399918
Group ID:
EG000
Title:
Everolimus and Bevacizumab
Description:
This is a single-institution, single-arm phase II trial of everolimus in combination with bevacizumab in patients with advanced non-clear cell RCC, who have not received prior VEGF-.or mTOR-targeted therapy.
Deaths Number Affected:
43
Deaths Number At Risk:
None
Serious Number Affected:
22
Serious Number At Risk:
55
Other Number Affected:
55
Other Number At Risk:
55
Study:
NCT01399918
Results Section:
NCT01399918
Adverse Events Module:
NCT01399918