The MASA Valve Early Feasibility Study (MVEFS) multi-site interventional clinical trial within the United States of America with each center following a common protocol.The objective of the trial is to evaluate the safety and probable benefit of MASA Valve in the indicated subset of patients requiring Right Ventricular Outflow Tract Reconstruction (RVOTR). As an early feasibility study, the purpose is determine the feasibility of success of the device in order to gather early data towards a future pivotal study and/or regulatory clearance submission.
The MASA Valve is a bi-leaflet pulmonary valved conduit. The MASA Valve has an ePTFE conduit and ePTFE leaflets fixtured to the conduit with polypropylene suture. The device has a pad-printed design on the outer conduit surface indicating the valve position and direction of flow. . The MASA Valve is intended to be used to reconstruction the Right Ventricular Outflow Tract (RVOT) and provide a functional pulmonary valve. Once implanted, the MASA Valve provides a pathway for blood from the Right Ventricle (RV) to the Pulmonary Arteries (PAs), while the integrated valve helps to prevent backflow into the RV. The MASA Valve Indications for Use are: The MASA Valve pulmonary valved conduit is indicated for correction or reconstruction of the right ventricular outflow tract (RVOT) in patients aged less than 22 years with any of the following congenital cardiac malformations: * Pulmonary Stenosis * Tetralogy of Fallot * Truncus Arteriosus * Transposition of Great Vessels * Pulmonary Atresia In addition, the MASA Valve is indicated for the replacement of previously implanted, but dysfunctional, pulmonary valves, valved conduits or conduits, as well as for use in the Ross Procedure when the native RVOT is being used to reconstruct the Aorta. Treatments currently available for the above-stated conditions include biologic-tissue-based valved conduits (Homografts and Contegra Glutaraldehyde-fixed Bovine Jugular Vein), Intra-operatively constructed valved conduits made from off-the-shelf vascular grafts and cardiovascular membranes, and non-valved cardiovascular conduits. Based on existing evidence it is believed the potential benefits of MASA Valve outweigh the potential risks.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
10
Surgical replacement of the Pulmonary Valve or a previously implanted prosthetic with the investigational device (MASA Valve)
OSF Childrens Hospital of Illinois
Peoria, Illinois, United States
RECRUITINGBoston Childrens Hospital
Boston, Massachusetts, United States
RECRUITINGCincinnati Children's Hospital
Cincinnati, Ohio, United States
RECRUITINGChildrens Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
RECRUITINGChildrens Medical Center Dallas
Dallas, Texas, United States
RECRUITINGFreedom from device related death
Percentage of patients that have not died related to the device 1 year from implantation
Time frame: 1 year
Freedom from Explant
Percentage of patients that have not undergone device explant within 1 year from implantation
Time frame: 1 year
Freedom from Device-Related Reoperation
Percentage of patients that have not undergone re-operation related to the device within 1 year from implantation
Time frame: 1 year
Freedom from Device-Related Catheter Intervention
Percentage of patients that have not undergone device related catheter based intervention within 1 year from implantation
Time frame: 1 year
Freedom from Endocarditis
Percentage of patients that have not had endocarditis within 1 year from implantation
Time frame: 1 year
Freedom from Thrombus
Percentage of patients that have not had a serious thrombotic event related to the device within 1 year from implantation
Time frame: 1 year
Freedom from Major Hemorrhage
Percentage of patients that have not had a major bleeding episode related to the device within 1 year from implantation
Time frame: 1 year
Freedom from Moderate or Greater Pulmonary Regurgitation
Percentage of patients that show less than Moderate Pulmonary Regurgitation within 1 year from implantation on Echocardiographic assessment
Time frame: 1 year
Freedom from Pulmonary Gradient ≥36mmHg
Percentage of patients that have a Pulmonary Gradient \<= 36mmHg within 1 year from implantation on Echocardiographic assessment
Time frame: 1 year
Freedom from device valve failure
Percentage of patients that show do not show valve functional failure on Echocardiographic assessment
Time frame: 1 year
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