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 @ 4:01 PM
Ignite Modification Date:
2025-12-25 @ 2:04 PM
NCT ID:
NCT03988166
Group ID:
EG000
Title:
Chronic Total Occlusion Percutaneous Coronary Intervention
Description:
CTO percutaneous coronary intervention (PCI) in which at least one Teleflex guidewire and at least one Turnpike catheter are used.
Chronic Total Occlusion Revascularization: Teleflex's series of study guidewires and catheters will be used to facilitate the safe and effective crossing of de novo CTOs and placement of conventional guidewires beyond the lesion via either a true lumen or subintimal pathway.
GuideLiner® V3 catheter, TrapLiner® catheter, Turnpike® catheter: GuideLiner® V3 catheter, TrapLiner® catheter, Turnpike® catheter
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
150
Other Number Affected:
0
Other Number At Risk:
150
Study:
NCT03988166
Results Section:
NCT03988166
Adverse Events Module:
NCT03988166