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 @ 2:58 AM
Ignite Modification Date:
2025-12-26 @ 1:39 AM
NCT ID:
NCT03041233
Group ID:
EG000
Title:
Enrolled
Description:
Patients who have indication for ablation of atrial fibrillation and who were willing to provide a written consent form, except pregnant women, were included in this registry. Patients were considered enrolled in this registry at the time they signed the written consent form.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
30
Serious Number At Risk:
833
Other Number Affected:
1
Other Number At Risk:
833
Study:
NCT03041233
Results Section:
NCT03041233
Adverse Events Module:
NCT03041233