Disrupt CAD III Post-Approval Study (PAS)
NCT05021757 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1212
Last updated 2024-02-01
Summary
The study design is a prospective, multicenter, observational, single-arm post-approval study using data collected in the National Cardiovascular Data Registry (NCDR®) CathPCI Registry®.
Conditions
Interventions
- DEVICE
-
Shockwave C2 Coronary IVL
PCI procedure using a Shockwave C2 coronary IVL catheter
Sponsors & Collaborators
-
Shockwave Medical, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-03-10
- Primary Completion
- 2022-03-31
- Completion
- 2022-03-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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