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 @ 7:42 PM
Ignite Modification Date:
2025-12-25 @ 5:21 PM
NCT ID:
NCT01651403
Group ID:
EG000
Title:
TDF (Blinded Randomized Phase)
Description:
Blinded Randomized Phase: TDF tablet or oral powder once daily (up to 300 mg depending on weight) for 72 weeks (protocol amendment 2) or 48 weeks (protocol amendment 3)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
60
Other Number Affected:
38
Other Number At Risk:
60
Study:
NCT01651403
Results Section:
NCT01651403
Adverse Events Module:
NCT01651403