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 @ 11:30 PM
Ignite Modification Date:
2025-12-25 @ 9:18 PM
NCT ID:
NCT00709956
Group ID:
EG001
Title:
Placebo / Iloprost (5 µg)
Description:
Single dose double-blind placebo on study day 2 followed by single dose double-blind active iloprost (5µg) on study day 3
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
33
Other Number Affected:
20
Other Number At Risk:
33
Study:
NCT00709956
Results Section:
NCT00709956
Adverse Events Module:
NCT00709956