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 @ 7:34 PM
Ignite Modification Date:
2025-12-25 @ 5:16 PM
NCT ID:
NCT02348203
Group ID:
EG001
Title:
Arm II (Double Placebo)
Description:
Patients receive aspirin placebo PO QD and zileuton placebo PO BID for 12 weeks.
Laboratory Biomarker Analysis: Correlative studies
Placebo Administration: Given aspirin placebo PO
Placebo Administration: Given zileuton placebo PO
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
32
Other Number Affected:
17
Other Number At Risk:
32
Study:
NCT02348203
Results Section:
NCT02348203
Adverse Events Module:
NCT02348203