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 @ 12:16 PM
Ignite Modification Date:
2025-12-25 @ 12:01 PM
NCT ID:
NCT01808261
Group ID:
EG001
Title:
GSK249320 15 mg/kg
Description:
Participants received GSK249320 15 mg/kg administered as two IV infusions, the first on Study Day 1 which is 24-72 post-stroke onset, and the second on Study Day 6 (+/- 2 days). Each 100 mL IV infusion was delivered over a period of 75 minutes (a 60 minute infusion followed by a 10 to 15 minute flush).
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
65
Other Number Affected:
32
Other Number At Risk:
65
Study:
NCT01808261
Results Section:
NCT01808261
Adverse Events Module:
NCT01808261