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 @ 2:00 AM
Ignite Modification Date:
2025-12-26 @ 12:23 AM
NCT ID:
NCT01728194
Group ID:
EG000
Title:
MDD (Escitalopram Tx)
Description:
Target dose 20mg for 12 weeks
Escitalopram: 20 mg target dose for 12 weeks
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
54
Other Number Affected:
9
Other Number At Risk:
54
Study:
NCT01728194
Results Section:
NCT01728194
Adverse Events Module:
NCT01728194