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 @ 7:15 PM
Ignite Modification Date:
2025-12-25 @ 4:52 PM
NCT ID:
NCT00474903
Group ID:
EG001
Title:
Arm II (Low-dose Aspirin, Placebo, Esomeprazole Magnesium)
Description:
Patients receive both an oral placebo and acetylsalicylic acid (81 mg dose), once daily and oral esomeprazole magnesium (40 mg, twice daily).
acetylsalicylic acid: Given orally esomeprazole magnesium: Given orally placebo: Given orally
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
45
Other Number Affected:
9
Other Number At Risk:
45
Study:
NCT00474903
Results Section:
NCT00474903
Adverse Events Module:
NCT00474903