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 @ 12:33 AM
Ignite Modification Date:
2025-12-25 @ 10:40 PM
NCT ID:
NCT00293267
Group ID:
EG000
Title:
Raltegravir 400 mg b.i.d Plus OBT
Description:
Includes all participants initially randomized to raltegravir, including those without virologic failure who
continued into the open-label phase at Week 156 and those who entered the OLPVF phase due to virologic failure. During either open-label phase up to Week 240, these participants continued to receive raltegravir 400 mg b.i.d. plus OBT.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
97
Serious Number At Risk:
232
Other Number Affected:
206
Other Number At Risk:
232
Study:
NCT00293267
Results Section:
NCT00293267
Adverse Events Module:
NCT00293267