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 @ 6:40 PM
Ignite Modification Date:
2025-12-25 @ 4:11 PM
NCT ID:
NCT05021757
Group ID:
EG000
Title:
Disrupt CAD III PAS Cohort
Description:
Patients in the CathPCI Registry who undergo a PCI procedure using a Shockwave C2 Coronary IVL catheter and meeting the eligibility criteria will be included in the PAS cohort. A minimum of 150 patients with 30-day follow-up will be included in the PAS cohort.
Shockwave C2 Coronary IVL: PCI procedure using a Shockwave C2 coronary IVL catheter
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
1212
Other Number Affected:
0
Other Number At Risk:
1212
Study:
NCT05021757
Results Section:
NCT05021757
Adverse Events Module:
NCT05021757