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 @ 7:49 PM
Ignite Modification Date:
2025-12-25 @ 5:25 PM
NCT ID:
NCT01781403
Group ID:
EG001
Title:
Dose Level 2
Description:
Capecitabine was given 825 mg/m\^2 twice/day during radiotherapy with drug holidays (weekend breaks).
Temozolomide was given 60 mg/m\^2 once/day during radiotherapy with drug holidays (weekend breaks).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
2
Other Number Affected:
2
Other Number At Risk:
2
Study:
NCT01781403
Results Section:
NCT01781403
Adverse Events Module:
NCT01781403