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:
2025-12-25 @ 4:48 AM
Ignite Modification Date:
2025-12-26 @ 3:50 AM
NCT ID:
NCT00088218
Group ID:
EG001
Title:
Clofarabine Plus Ara-C
Description:
Clofarabine IV 30 mg/m\^2 daily times 5 days + Ara-C 20 mg/m\^2 subcutaneously daily times 14 days.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
39
Serious Number At Risk:
79
Other Number Affected:
54
Other Number At Risk:
79
Study:
NCT00088218
Results Section:
NCT00088218
Adverse Events Module:
NCT00088218