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 @ 12:17 AM
Ignite Modification Date:
2025-12-25 @ 10:19 PM
NCT ID:
NCT01710358
Group ID:
EG007
Title:
Placebo Follow-up
Description:
No study drug received. Participants return for safety follow-up visit 28 days after the last dose of study drug.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
33
Other Number Affected:
3
Other Number At Risk:
33
Study:
NCT01710358
Results Section:
NCT01710358
Adverse Events Module:
NCT01710358