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 @ 3:38 PM
Ignite Modification Date:
2025-12-25 @ 1:49 PM
NCT ID:
NCT03759392
Group ID:
EG000
Title:
Omecamtiv Mecarbil
Description:
Omecamtiv mecarbil was administered as an oral modified-release tablet twice daily for up to 20 weeks. Participants randomized to this arm started at an omecamtiv mecarbil dose of 25 mg twice daily. The dose could be increased based on plasma concentrations at Weeks 2 and 6.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
30
Serious Number At Risk:
185
Other Number Affected:
126
Other Number At Risk:
185
Study:
NCT03759392
Results Section:
NCT03759392
Adverse Events Module:
NCT03759392