Coroflex ISAR NEO "All Comers" Post Market Clinical Follow-up (PMCF)
NCT03809715 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3520
Last updated 2026-01-08
Summary
The aim of the study is to assess the safety and efficacy of the device to treat coronary de novo and restenotic lesions.
Conditions
Interventions
- DEVICE
-
Coroflex® ISAR NEO coronary stent system
treatment of coronary artery disease with Coroflex® ISAR NEO of "real world" de-novo and restenotic lesions in native coronary arteries and coronary bypass grafts
Sponsors & Collaborators
-
B. Braun Melsungen AG
lead INDUSTRY
Principal Investigators
-
Rene Koning, MD · Clinique St. Hilaire
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-01-17
- Primary Completion
- 2024-05-31
- Completion
- 2025-08-15
Countries
- France
Study Locations
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