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 @ 4:44 PM
Ignite Modification Date:
2025-12-25 @ 2:31 PM
NCT ID:
NCT00686166
Group ID:
EG000
Title:
Chemotherapy
Description:
Patients receive oxaliplatin 50 mg/m\^2 IV (Days 1, 8, 15, 22, 29), cetuximab 400 mg/m\^2 IV (Day 1), cetuximab 250 mg/m\^2 IV (Days 8, 15, 22, 29), capecitabine 1650 mg/m\^2 PO (Monday-Friday, Day 1-35). Cycle is 35 days, followed by a 14-day break.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
74
Other Number Affected:
73
Other Number At Risk:
74
Study:
NCT00686166
Results Section:
NCT00686166
Adverse Events Module:
NCT00686166