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 @ 4:18 AM
Ignite Modification Date:
2025-12-26 @ 3:19 AM
NCT ID:
NCT00667420
Group ID:
EG000
Title:
Epirubicin, Oxaliplatin, Capecitabine, Panitumumab Treatment
Description:
Panitumumab in Combination with Epirubicin, Oxaliplatin and Capecitabine (EOX-P)
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
17
Other Number Affected:
13
Other Number At Risk:
17
Study:
NCT00667420
Results Section:
NCT00667420
Adverse Events Module:
NCT00667420