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 @ 4:18 AM
Ignite Modification Date:
2025-12-26 @ 3:18 AM
NCT ID:
NCT02480920
Group ID:
EG000
Title:
Advers Events
Description:
The adverse effects, stroke, and any bleeding complication during NOAC treatment. Major bleeding was defined as a hemorrhage leading to a reduction in hemoglobin concentration of 2 g/dL, necessitating the transfusion of 2 or more units of blood, or symptomatic bleeding into a critical area or organ.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
687
Serious Number At Risk:
2738
Other Number Affected:
0
Other Number At Risk:
2738
Study:
NCT02480920
Results Section:
NCT02480920
Adverse Events Module:
NCT02480920