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 @ 12:00 PM
Ignite Modification Date:
2025-12-25 @ 11:57 AM
NCT ID:
NCT00961961
Group ID:
EG000
Title:
Lithium Plus Fluoxetine Phase I
Description:
This is the condition that all participants started in. They were given Lithium plus Fluoxetine and, if they responded, they were asked to accept random assignment to Phase II.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
177
Other Number Affected:
0
Other Number At Risk:
177
Study:
NCT00961961
Results Section:
NCT00961961
Adverse Events Module:
NCT00961961