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 @ 3:37 PM
Ignite Modification Date:
2025-12-25 @ 1:49 PM
NCT ID:
NCT02946892
Group ID:
EG000
Title:
Carvedilol
Description:
Study participants will receive carvedilol for 12 weeks
Carvedilol: Carvedilol will be given for 12 weeks and then an exercise test will be performed
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
25
Other Number Affected:
4
Other Number At Risk:
25
Study:
NCT02946892
Results Section:
NCT02946892
Adverse Events Module:
NCT02946892