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 @ 4:07 AM
Ignite Modification Date:
2025-12-26 @ 3:04 AM
NCT ID:
NCT01950520
Group ID:
EG016
Title:
Cohort 3 : Placebo
Description:
Interventions, in random order, will be administered during one of the four overnight inpatient stays
Mirabegron 50mg: Mirabegron 50mg, oral, by mouth (Cohort 3 only)
Mirabegron 200mg: Mirabegron 200mg, oral, by mouth (Cohort 3 only)
Placebo for Mirabegron: Placebo for Mirabegron, oral, by mouth (Cohort 3 only)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
13
Other Number Affected:
1
Other Number At Risk:
13
Study:
NCT01950520
Results Section:
NCT01950520
Adverse Events Module:
NCT01950520