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 @ 11:35 PM
Ignite Modification Date:
2025-12-25 @ 9:25 PM
NCT ID:
NCT03095456
Group ID:
EG001
Title:
Spiriva Handihaler®
Description:
Active Spiriva Handihaler® and placebo (in place of Revefenacin)
Spiriva Handihaler®: Spiriva Handihaler® contains Spiriva (also known as Tiotropium) and is administered via HandiHaler® device.
Placebo for Revefenacin: Placebo administered as double blind, double dummy via nebulization.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
104
Other Number Affected:
21
Other Number At Risk:
104
Study:
NCT03095456
Results Section:
NCT03095456
Adverse Events Module:
NCT03095456