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 @ 4:33 AM
Ignite Modification Date:
2025-12-26 @ 3:35 AM
NCT ID:
NCT02991118
Group ID:
EG000
Title:
Placebo
Description:
Participants received placebo tablet once daily by mouth for 4 weeks prior to the 52-week double-blind treatment period. During the treatment period, participants received placebo once daily by mouth for 52 weeks. Participants remained on ongoing lipid-modifying therapy (not study provided) throughout the study.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
48
Serious Number At Risk:
257
Other Number Affected:
88
Other Number At Risk:
257
Study:
NCT02991118
Results Section:
NCT02991118
Adverse Events Module:
NCT02991118