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 @ 1:06 PM
Ignite Modification Date:
2025-12-25 @ 12:21 PM
NCT ID:
NCT04211961
Group ID:
EG001
Title:
Scopolamine
Description:
Participants randomised to the treatment group will receive one 15-minute IV infusion of Scopolamine (dose 4μg/kg) at 4 visits.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
26
Other Number Affected:
25
Other Number At Risk:
26
Study:
NCT04211961
Results Section:
NCT04211961
Adverse Events Module:
NCT04211961