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 @ 12:56 PM
Ignite Modification Date:
2025-12-25 @ 12:18 PM
NCT ID:
NCT00376961
Group ID:
EG000
Title:
Rituximab-CHOP-Bortezomib (R-CHOP-V) Induction
Description:
Rituximab-CHOP-Bortezomib (R-CHOP-V) induction is administered every 21 days for 6 cycles (1 cycle= 21 days)
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
65
Other Number Affected:
64
Other Number At Risk:
65
Study:
NCT00376961
Results Section:
NCT00376961
Adverse Events Module:
NCT00376961