Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm
NCT01156272 · Status: WITHDRAWN · Type: OBSERVATIONAL
Last updated 2015-08-06
Summary
The purpose of this study is to evaluate the safety and efficacy of the ATS 3f® Aortic Bioprosthesis, Model 1000 (Equine Pericardial Bioprothesis) size 19mm in a patient population undergoing isolated aortic valve replacement of his/her native aortic valve, or replacement of a failed prosthesis.
Conditions
- Heart Valve Diseases
Interventions
- DEVICE
-
ATS Medical 3f® Aortic Bioprosthesis, Model 1000 19mm
Replacement aortic heart valve
Sponsors & Collaborators
-
Medtronic Cardiovascular
lead INDUSTRY
Principal Investigators
-
Mike Boulware, PhD · Medtronic
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-06-30
- Primary Completion
- 2011-06-30
- Completion
- 2011-06-30
Countries
- Canada
Study Locations
More Related Trials
-
Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical SWIFT HM3 PMS
NCT04548128 ·Status: COMPLETED
-
Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement
NCT01240902 ·Status: COMPLETED ·Phase: NA
-
Clinical Investigation Of The Mitroflow Aortic Pericardial Heart Valve
NCT00630916 ·Status: COMPLETED ·Phase: NA
-
Perceval S Aortic Heart Valve Study- North America
NCT01810679 ·Status: TERMINATED ·Phase: NA
-
Early Feasibility Study of the Cardiovalve System for Tricuspid Regurgitation
NCT04100720 ·Status: WITHDRAWN ·Phase: NA
-
Observational Study of the Heart Repair Technologies Mitral Bridge in Treating Mitral Valve Regurgitation
NCT03511716 ·Status: TERMINATED
-
PARTNER 3 Trial - Mitral Valve in Valve
NCT03193801 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Edwards SAPIEN-3 Periprosthetic Leakage Evaluation Versus Medtronic CoreValve in Transfemoral Aortic Valve Implantation
NCT01982032 ·Status: TERMINATED ·Phase: NA
-
Streamlined One-wire Logistics Optimize Transcatheter Aortic Valve Replacement
NCT07090811 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Safety and Performance of TAVI of Venus MedTech Aortic Valve Prosthesis
NCT01683474 ·Status: UNKNOWN ·Phase: NA
-
Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study
NCT03635424 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Mitroflow DL Post Approval Study- North America
NCT02351726 ·Status: TERMINATED ·Phase: NA
-
First in Man Study of the JenaValve TAVI Plus System Transfemoral
NCT02818959 ·Status: TERMINATED ·Phase: NA
-
Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Position
NCT00477555 ·Status: COMPLETED
-
Transmural Systems Transcaval Closure Device for Transcaval Access Ports During Transcatheter Aortic Valve Replacement
NCT03432494 ·Status: TERMINATED ·Phase: NA
-
Cardiovalve Transfemoral Mitral Valve System
NCT03813524 ·Status: TERMINATED ·Phase: NA
-
Feasibility Study of Patients With Severe MR Treated With the Cardiovalve TMVR System
NCT03714412 ·Status: WITHDRAWN ·Phase: NA
-
Transfemoral Replacement of Aortic Valve With HLT MeriDIAN Valve Early Feasibility Trial
NCT02799823 ·Status: TERMINATED ·Phase: NA
-
Edwards PASCAL Transcatheter Valve Repair System Pivotal Clinical Trial
NCT04097145 ·Status: RECRUITING ·Phase: NA
-
U.S. Multicenter Feasibility Trial of the F2 Filter and Delivery System for Embolic Protection During TAVR
NCT06069661 ·Status: WITHDRAWN ·Phase: NA
-
COMPASSION S3 - Evaluation of the SAPIEN 3 Transcatheter Heart Valve in Patients With Pulmonary Valve Dysfunction
NCT02744677 ·Status: RECRUITING ·Phase: NA
-
TranScatheter Aortic Valve RepLacement System US Feasibility Trial
NCT01932099 ·Status: UNKNOWN ·Phase: PHASE2
-
Heart Leaflet Technologies Valve Study
NCT00710775 ·Status: UNKNOWN ·Phase: NA
-
Medtronic Evolut™ EXPAND TAVR I Feasibility Study
NCT04639258 ·Status: TERMINATED ·Phase: NA
-
REDUCE LAP-HF III Corvia Protocol 1701
NCT03191656 ·Status: ACTIVE_NOT_RECRUITING