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 @ 2:30 AM
Ignite Modification Date:
2025-12-26 @ 1:05 AM
NCT ID:
NCT01302834
Group ID:
EG001
Title:
IMRT + Cetuximab
Description:
Intensity-modulated radiotherapy (IMRT) with concurrent cetuximab
Cetuximab: 400 mg/m2 IV 5-7 days before IMRT then 250 mg/m2 IV weekly for 7 weeks
IMRT: 35 fractions over 6 weeks, 6 fractions per week, 2 Gray per fraction to total dose of 70 Gy.
Deaths Number Affected:
86
Deaths Number At Risk:
None
Serious Number Affected:
115
Serious Number At Risk:
394
Other Number Affected:
393
Other Number At Risk:
394
Study:
NCT01302834
Results Section:
NCT01302834
Adverse Events Module:
NCT01302834