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 @ 6:40 PM
Ignite Modification Date:
2025-12-25 @ 4:11 PM
NCT ID:
NCT02237157
Group ID:
EG001
Title:
Gemcitabine, Local Delivery (Dose 2)
Description:
Gemcitabine; 1 cycle, two doses per cycle; 500mg/m2 dose
Gemcitabine, local delivery: Intra-arterial targeted drug delivery
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
15
Other Number Affected:
7
Other Number At Risk:
15
Study:
NCT02237157
Results Section:
NCT02237157
Adverse Events Module:
NCT02237157