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 @ 11:10 PM
Ignite Modification Date:
2025-12-25 @ 8:44 PM
NCT ID:
NCT03924869
Group ID:
EG001
Title:
Placebo + SBRT
Description:
Participants received SBRT once every 3 days for 3, 4, 5, or 8 fractions (dependent on tumor type/location; 45-70 Gy total) over approximately 2 weeks PLUS placebo (normal saline solution) via IV infusion once every 3 weeks for up to 17 cycles (up to approximately 1 year). Each cycle was 21 days.
Deaths Number Affected:
63
Deaths Number At Risk:
None
Serious Number Affected:
74
Serious Number At Risk:
218
Other Number Affected:
176
Other Number At Risk:
218
Study:
NCT03924869
Results Section:
NCT03924869
Adverse Events Module:
NCT03924869