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 @ 4:58 AM
Ignite Modification Date:
2025-12-26 @ 3:57 AM
NCT ID:
NCT01613118
Group ID:
EG003
Title:
Irbesartan 300 mg - Double-Blind Period
Description:
The control irbesartan was administered as a single oral dose of 150mg for the first week before escalating to 300mg for the remaining 7 weeks.
Patients at \</= 50kg received 150mg irbesartan for the 8 week duration.
Irbesartan: Oral, once-daily
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
36
Other Number Affected:
26
Other Number At Risk:
36
Study:
NCT01613118
Results Section:
NCT01613118
Adverse Events Module:
NCT01613118