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 @ 3:52 PM
Ignite Modification Date:
2025-12-25 @ 1:57 PM
NCT ID:
NCT01856192
Group ID:
EG000
Title:
Arm A (R2CHOP)
Description:
Patients receive rituximab IV, cyclophosphamide IV, doxorubicin hydrochloride IV, and vincristine sulfate IV on day 1; prednisone PO on days 1-5; and lenalidomide PO on days 1-10. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.
Deaths Number Affected:
36
Deaths Number At Risk:
None
Serious Number Affected:
128
Serious Number At Risk:
166
Other Number Affected:
164
Other Number At Risk:
166
Study:
NCT01856192
Results Section:
NCT01856192
Adverse Events Module:
NCT01856192