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 @ 5:12 PM
Ignite Modification Date:
2025-12-25 @ 2:50 PM
NCT ID:
NCT00441350
Group ID:
EG000
Title:
Phase B OM/HCTZ 40/12.5 mg Non-responders
Description:
Phase B (second double-blind treatment phase, 8 weeks duration):
Non-responders to OM/HCTZ 40/12.5 mg treatment were to be up- titrated to OM/HCTZ 40/25 mg.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
188
Other Number Affected:
9
Other Number At Risk:
188
Study:
NCT00441350
Results Section:
NCT00441350
Adverse Events Module:
NCT00441350