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 @ 8:02 PM
Ignite Modification Date:
2025-12-25 @ 5:35 PM
NCT ID:
NCT03099304
Group ID:
EG001
Title:
Ruxolitinib Cream 0.15% Once Daily (QD)
Description:
All participants who received at least one dose of ruxolitinib cream 0.15% QD (in the 52-week combined vehicle-controlled and continued double-blind periods).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
31
Other Number Affected:
19
Other Number At Risk:
31
Study:
NCT03099304
Results Section:
NCT03099304
Adverse Events Module:
NCT03099304