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 @ 7:02 PM
Ignite Modification Date:
2025-12-25 @ 4:35 PM
NCT ID:
NCT03829657
Group ID:
EG004
Title:
RW Treatment Period: Ampreloxetine
Description:
Participants who completed the OL treatment period and were randomized to receive 10 mg oral ampreloxetine QD for a further 6 weeks in the RW treatment period.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
64
Other Number Affected:
17
Other Number At Risk:
64
Study:
NCT03829657
Results Section:
NCT03829657
Adverse Events Module:
NCT03829657