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 @ 1:43 AM
Ignite Modification Date:
2025-12-26 @ 12:00 AM
NCT ID:
NCT00234494
Group ID:
EG000
Title:
Single Group Assignment
Description:
Cisplatin + Gemcitabine + Bevacizumab
Cisplatin: Cisplatin 70 mg/m2, day 1
Gemcitabine: Gemcitabine 1250 mg/m2, day 1 and 8
Bevacizumab: Bevacizumab 15mg/kg, day 1
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
26
Serious Number At Risk:
45
Other Number Affected:
43
Other Number At Risk:
45
Study:
NCT00234494
Results Section:
NCT00234494
Adverse Events Module:
NCT00234494