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:
2025-12-25 @ 1:15 AM
Ignite Modification Date:
2025-12-25 @ 11:24 PM
NCT ID:
NCT00184093
Group ID:
EG000
Title:
Gemcitabine Weekly x 6 Wks With Concurrent External Radiation
Description:
Gemcitabine 350 mg/m2 IV weekly x 6 weeks with concurrent external radiation
Gemcitabine: Gemcitabine weekly x 6 wks with concurrent external radiation
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
35
Other Number Affected:
33
Other Number At Risk:
35
Study:
NCT00184093
Results Section:
NCT00184093
Adverse Events Module:
NCT00184093