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:
EG000
Title:
Experimental: Cohort A
Description:
Under Protocol version 1.0:
No resistance to NRTIs, PIs, or NNRTI
• Continue current second-line regimen; NRTIs could be modified
Changed under LOA#2 to:
No LPV/RTV resistance and susceptible to at least one NRTI, regardless of NNRTI resistance or prior RAL exposure • Continue second-line regimen which may include LPV/RTV; NRTIs could be modified
Changed under LOA#3 to:
No LPV/RTV resistance and susceptible to at least one NRTI, regardless of NNRTI resistance or prior RAL exposure
• Continue PI backbone; NRTIs could be modified. If on a RAL-containing regimen, RAL must be discontinued.
Deaths Number Affected:
18
Deaths Number At Risk:
None
Serious Number Affected:
61
Serious Number At Risk:
287
Other Number Affected:
283
Other Number At Risk:
287
Study:
NCT01641367
Results Section:
NCT01641367
Adverse Events Module:
NCT01641367