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 @ 9:30 PM
Ignite Modification Date:
2025-12-25 @ 7:15 PM
NCT ID:
NCT05103332
Group ID:
EG002
Title:
Run-in: Olmesartan
Description:
Participants who cleared screening received open-label therapy with olmesartan 40 mg orally QD \[or 20 mg orally QD for participants with creatinine clearance ≤ 60 mL/min at screening enrolled at sites outside of the US\] as their protocol-specified background antihypertensive medication during a Run-in period of at least 4 weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
293
Other Number Affected:
0
Other Number At Risk:
293
Study:
NCT05103332
Results Section:
NCT05103332
Adverse Events Module:
NCT05103332