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 @ 2:32 AM
Ignite Modification Date:
2025-12-26 @ 1:08 AM
NCT ID:
NCT01300234
Group ID:
EG001
Title:
ADV-TDF
Description:
In first double-blinded treatment period, participants self-administered ADV 10 mg tablets plus matching TDF placebo at the same time QD for 48 Weeks. In second open-label treatment period, participants self-administered TDF 300 mg QD for additional 192 Weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
252
Other Number Affected:
121
Other Number At Risk:
252
Study:
NCT01300234
Results Section:
NCT01300234
Adverse Events Module:
NCT01300234