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 @ 1:20 PM
Ignite Modification Date:
2025-12-25 @ 12:26 PM
NCT ID:
NCT02394795
Group ID:
EG001
Title:
Group B; mFOLFOX6 + Bevacizumab Combination Therapy
Description:
OXA: 85 mg/m2/day 1 l-LV: 200 mg/m2/day 1 5-FU iv: 400 mg/m2/day 1 5-FU civ: 2400 mg/m2/day 1-3 bevacizumab: 5 mg/kg/ mFOLFOX6 + bevacizumab combination therapy, once every two weeks.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
95
Serious Number At Risk:
407
Other Number Affected:
392
Other Number At Risk:
407
Study:
NCT02394795
Results Section:
NCT02394795
Adverse Events Module:
NCT02394795