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 @ 6:56 PM
Ignite Modification Date:
2025-12-25 @ 4:29 PM
NCT ID:
NCT04733157
Group ID:
EG000
Title:
Study Group/Group A_(Tranexamic Acid)
Description:
The study group will receive TXA 1g intravenously at the onset of skin incision.
Tranexamic acid injection: Tranexamic 1g administered intravenously at the onset of skin incision at caesarean section
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
611
Other Number Affected:
50
Other Number At Risk:
611
Study:
NCT04733157
Results Section:
NCT04733157
Adverse Events Module:
NCT04733157