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:
2025-12-25 @ 12:14 AM
Ignite Modification Date:
2025-12-25 @ 10:16 PM
NCT ID:
NCT01378858
Group ID:
EG000
Title:
Varenicline Treatment as Usual (TAU)
Description:
Subjects in the TAU arm will self administer varenicline for 12 weeks.
Varenicline: Varenicline, titrated to 1 mg twice daily, will be given to participants in both study arms for 12 weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
50
Other Number Affected:
50
Other Number At Risk:
50
Study:
NCT01378858
Results Section:
NCT01378858
Adverse Events Module:
NCT01378858