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 @ 12:16 PM
Ignite Modification Date:
2025-12-25 @ 12:02 PM
NCT ID:
NCT00665561
Group ID:
EG000
Title:
Maraviroc Exposed
Description:
Human immunodeficiency virus- 1( HIV-1) infected, treatment-experienced adult participants, who were prescribed with maraviroc along with an optimized background antiretroviral therapy (OBT) regimen (in usual clinical practice following the approved local label of maraviroc), were included in this study and were observed in this study for an observation period of up to 5 years following enrollment.
Deaths Number Affected:
75
Deaths Number At Risk:
None
Serious Number Affected:
435
Serious Number At Risk:
1316
Other Number Affected:
111
Other Number At Risk:
1316
Study:
NCT00665561
Results Section:
NCT00665561
Adverse Events Module:
NCT00665561