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 @ 5:49 PM
Ignite Modification Date:
2025-12-25 @ 3:15 PM
NCT ID:
NCT01781468
Group ID:
EG001
Title:
Arm II (250 mg Armodafinil)
Description:
Patients receive 250 mg Armodafinil orally every day in the morning for 8 weeks.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
110
Other Number Affected:
60
Other Number At Risk:
110
Study:
NCT01781468
Results Section:
NCT01781468
Adverse Events Module:
NCT01781468