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:
2025-12-24 @ 10:04 PM
Ignite Modification Date:
2025-12-25 @ 7:40 PM
NCT ID:
NCT00590135
Group ID:
EG000
Title:
AORTIC STENOSIS PATIENTS
Description:
Patients with mild to moderate calcific aortic stenosis will receive atorvastatin 40 mg by mouth once daily
atorvastatin (Lipitor): atorvastatin 40 mg by mouth once daily
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
59
Other Number Affected:
0
Other Number At Risk:
59
Study:
NCT00590135
Results Section:
NCT00590135
Adverse Events Module:
NCT00590135