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 @ 12:42 PM
Ignite Modification Date:
2025-12-25 @ 12:13 PM
NCT ID:
NCT01570361
Group ID:
EG001
Title:
Antiarrhythmic Drug (AAD) Therapy Only
Description:
Antiarrhythmic Drug therapy (either rate or rhythm control): Class I or class III, or AV nodal blocking agents such as beta blockers and calcium channel blockers in accordance with 2006 atrial fibrillation management guidelines. This group includes only those subjects received AAD only.
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
30
Serious Number At Risk:
108
Other Number Affected:
43
Other Number At Risk:
108
Study:
NCT01570361
Results Section:
NCT01570361
Adverse Events Module:
NCT01570361