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:
2025-12-26 @ 10:56 AM
Ignite Modification Date:
2025-12-26 @ 10:56 AM
NCT ID:
NCT03547908
Group ID:
EG001
Title:
Blinded Phase: DTG + F/TDF
Description:
Participants who were HIV-1 and HBV coinfected and treatment-naïve received DTG (50 mg) tablet + F/TDF (200/300 mg) FDC tablet, orally, once daily without regard to food for 96 weeks. Participants also received PTM B/F/TAF tablet, orally, once daily without regard to food for 96 weeks.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
122
Other Number Affected:
98
Other Number At Risk:
122
Study:
NCT03547908
Results Section:
NCT03547908
Adverse Events Module:
NCT03547908