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 @ 12:43 AM
Ignite Modification Date:
2025-12-25 @ 10:54 PM
NCT ID:
NCT01641367
Group ID:
EG005
Title:
Experimental: Cohort D
Description:
Under Protocol version 1.0:
Multiple NRTI resistance and/or DRV/RTV resistance or prior RAL exposure:
• Best available regimen, including study-provided and any locally available drugs
Changed under LOA#2:
Not eligible for Cohort A, B, or C:
• Best available regimen, including study-provided and any locally available drugs
Updated under protocol v2.0:
• Best available ART regimen, including study-provided and any locally available non-experimental drugs
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
34
Other Number Affected:
33
Other Number At Risk:
34
Study:
NCT01641367
Results Section:
NCT01641367
Adverse Events Module:
NCT01641367