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 @ 2:29 PM
Ignite Modification Date:
2025-12-25 @ 1:03 PM
NCT ID:
NCT01885559
Group ID:
EG001
Title:
ACE-I + ARB
Description:
ACE-I + ARB and standard blood pressure control of 110-130/80 mm Hg
Lisinopril and Telmisartan: Lisinopril titrated to 5mg, 10mg, 20mg, 40mg and telmisartan titrated to 40mg and 80mg, as tolerated by participants, to achieve standard blood pressure control of 110-130/80 mm Hg.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
88
Serious Number At Risk:
244
Other Number Affected:
60
Other Number At Risk:
244
Study:
NCT01885559
Results Section:
NCT01885559
Adverse Events Module:
NCT01885559