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 @ 2:27 AM
Ignite Modification Date:
2025-12-26 @ 1:01 AM
NCT ID:
NCT03988634
Group ID:
EG000
Title:
Double-blind Phase Sacubitril+ Valsartan (LCZ696)
Description:
Study treatment was titrated to the target dose of sacubitril/valsartan (LCZ696) 97/103 mg twice daily (Dose Level 3)
Deaths Number Affected:
18
Deaths Number At Risk:
None
Serious Number Affected:
119
Serious Number At Risk:
233
Other Number Affected:
161
Other Number At Risk:
233
Study:
NCT03988634
Results Section:
NCT03988634
Adverse Events Module:
NCT03988634