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 @ 3:53 AM
Ignite Modification Date:
2025-12-26 @ 2:42 AM
NCT ID:
NCT00687102
Group ID:
EG001
Title:
Star Participants Assigned to Raloxifene
Description:
Participants in the parent study, STAR assigned to Raloxifene who were 65 or older at time of enrollment.
raloxifene: oral raloxifene plus placebo daily for 5 years
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
765
Other Number Affected:
0
Other Number At Risk:
765
Study:
NCT00687102
Results Section:
NCT00687102
Adverse Events Module:
NCT00687102