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 @ 4:41 PM
Ignite Modification Date:
2025-12-25 @ 2:30 PM
NCT ID:
NCT03722966
Group ID:
EG001
Title:
Varenicline/Counseling (VAR+NREM)
Description:
Participants will receive behavioral tobacco cessation counseling, a 13-week course of varenicline, and no automated medication reminders.
Varenicline: All participants will be offered a 13-week course of varenicline (including a 1 week titration period). Dosage and administration per manufacturer: 0.5mg once daily for days 1-3 and 0.5mg twice daily for days 4-7 encompass the titration period, then 1mg twice daily for 12 weeks. An additional 12 weeks of treatment is recommended for long-term abstinence.
Tobacco Cessation Counseling: All participants will be offered 6 weekly tobacco cessation counseling sessions with a Tobacco Treatment Specialist.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
12
Other Number Affected:
3
Other Number At Risk:
12
Study:
NCT03722966
Results Section:
NCT03722966
Adverse Events Module:
NCT03722966