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:
2025-12-26 @ 10:17 PM
Ignite Modification Date:
2025-12-26 @ 10:17 PM
NCT ID:
NCT01271712
Group ID:
EG002
Title:
Placebo, Open Label Only (Switch to Regorafenib)
Description:
Participants switched to Open-label Regorafenib treatment from Placebo. Participants received Regorafenib (Stivarga) 160 mg (4 x 40 mg tablets) per os once daily, 3 weeks
Deaths Number Affected:
47
Deaths Number At Risk:
None
Serious Number Affected:
31
Serious Number At Risk:
58
Other Number Affected:
58
Other Number At Risk:
58
Study:
NCT01271712
Results Section:
NCT01271712
Adverse Events Module:
NCT01271712