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 @ 5:05 PM
Ignite Modification Date:
2025-12-25 @ 2:44 PM
NCT ID:
NCT01294150
Group ID:
EG000
Title:
UroLift System
Description:
The treatment group subjects underwent UroLift system procedure. The subject was blinded to the randomization of control or treatment group. Unblinding occurred at 3 months post procedure after the assessments were completed. All subjects will be followed at a minimum of 5 years per the assessment schedule.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
52
Serious Number At Risk:
140
Other Number Affected:
133
Other Number At Risk:
140
Study:
NCT01294150
Results Section:
NCT01294150
Adverse Events Module:
NCT01294150