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 @ 2:12 PM
Ignite Modification Date:
2025-12-25 @ 12:51 PM
NCT ID:
NCT00256295
Group ID:
EG000
Title:
Gemcitabine Plus Oxaliplatin
Description:
Gemcitabine given 1000 mg/m2 IV over 100 minutes Every 21 days. Oxaliplatin given 65 mg/m2 IV over 120 minutes immediately following gemcitabine Every 21 days.
Gemcitabine : 1000 mg/m2 IV over 100 minutes Every 21 days
Oxaliplatin : 65 mg/m2 IV over 120 minutes immediately following gemcitabine Every 21 days
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
7
Other Number Affected:
1
Other Number At Risk:
7
Study:
NCT00256295
Results Section:
NCT00256295
Adverse Events Module:
NCT00256295