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 @ 3:30 AM
Ignite Modification Date:
2025-12-26 @ 2:12 AM
NCT ID:
NCT02428205
Group ID:
EG000
Title:
Propranolol Arm
Description:
Allocated to propranolol (n=5)
Lost to follow-up (n=2)
* Withdrew after baseline visit due to not feeling seeing a benefit (n=1)
* Withdrew after 6-week visit -no reason given (n=1)
Completed (n=4 at 6 weeks) (n=3 at 12 weeks)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
5
Other Number Affected:
1
Other Number At Risk:
5
Study:
NCT02428205
Results Section:
NCT02428205
Adverse Events Module:
NCT02428205