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 @ 11:52 PM
Ignite Modification Date:
2025-12-25 @ 9:47 PM
NCT ID:
NCT02370251
Group ID:
EG000
Title:
Omegaven
Description:
Children will receive Omegaven at a maximum of 1 g/kg/day upon enrollment in this arm.
Omegaven: Once the direct bilirubin is 2 mg/dL or more x 2 weeks, Intralipid will be switched to Omegaven at 1 g/kg/day. The bilirubin level will be monitored to determine when resolution of cholestasis (DB \<2 mg/dL) occurs.
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
52
Other Number Affected:
0
Other Number At Risk:
52
Study:
NCT02370251
Results Section:
NCT02370251
Adverse Events Module:
NCT02370251