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 @ 2:00 PM
Ignite Modification Date:
2025-12-25 @ 12:46 PM
NCT ID:
NCT02293395
Group ID:
EG000
Title:
Rivaroxaban 2.5 mg Twice Daily (BID)
Description:
Participants received oral dose of 2.5 mg rivaroxaban BID and acetylsalicylic acid (ASA) placebo once daily (OD) along with either clopidogrel 75 mg OD or ticagrelor 90 mg BID for a minimum of 180 days, and up to 360 days of treatment.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
125
Serious Number At Risk:
1510
Other Number Affected:
81
Other Number At Risk:
1510
Study:
NCT02293395
Results Section:
NCT02293395
Adverse Events Module:
NCT02293395