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 @ 6:29 PM
Ignite Modification Date:
2025-12-25 @ 3:59 PM
NCT ID:
NCT00955968
Group ID:
EG001
Title:
Stop HAART
Description:
Participants would stop receiving HAART after delivery or other pregnancy outcome and resume when protocol-specified criteria were met.
Highly active antiretroviral therapy (HAART): A combination of three or more HIV medications belonging to two or more drug classes
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
825
Other Number Affected:
765
Other Number At Risk:
825
Study:
NCT00955968
Results Section:
NCT00955968
Adverse Events Module:
NCT00955968