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 @ 10:13 PM
Ignite Modification Date:
2025-12-25 @ 7:48 PM
NCT ID:
NCT00678535
Group ID:
EG001
Title:
Capecitabine Plus Cisplatin
Description:
Cisplatin (3-week cycle, 80 mg/m\^2 intravenous infusion on Day 1) and capecitabine (3-week cycle, 1000 mg/m\^2 orally twice daily for 14 days) until documented disease progression, unacceptable toxicity, or withdrawal of consent.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
194
Serious Number At Risk:
436
Other Number Affected:
429
Other Number At Risk:
436
Study:
NCT00678535
Results Section:
NCT00678535
Adverse Events Module:
NCT00678535