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:
NCT03114995
Group ID:
EG001
Title:
Control C1 (High Platelet Reactivity - no Tirofiban)
Description:
Patients with high platelet reactivity unit (230 or higher) Tirofiban was not administered
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
30
Other Number Affected:
1
Other Number At Risk:
30
Study:
NCT03114995
Results Section:
NCT03114995
Adverse Events Module:
NCT03114995