Ireland
--:--IST
Recruiting Not applicable

MASA Valve Early Feasibility Study

NCT05452720 · tracked via the Priya Life Science USA tracker
Sponsor
PECA Labs
Phase
Not applicable
Started
2023-05-18
Last updated
2024-11-06

Condition(s) studied

Tetrology of FallotPulmonary StenosisTruncus ArteriosusTransposition of Great VesselsPulmonary AtresiaRoss Procedure

Investigational drug(s) / intervention(s)

Surgical Right Ventricular Outflow Tract Reconstruction

Surgical Right Ventricular Outflow Tract Reconstruction: Surgical replacement of the Pulmonary Valve or a previously implanted prosthetic with the investigational device (MASA Valve)

Study summary

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.

Eligibility

Sex
ALL
Min age
0 Years
Max age
22 Years
Healthy volunteers
No
Inclusion Criteria: 1. At least one of the following: Right Ventricular to Pulmonary Artery mean gradient \> 35mm Hg, moderate or severe Pulmonary regurgitation (≥3+), or clinical indication for replacement of their native or prosthetic pulmonary valve with a prosthesis. 2. Age \< 22 years 3. Patient is geographically stable and willing to return for 1 year follow-up for the trial. 4. Patient's legal guardian should be willing to provide informed consent (IC) at the hospital location where they are being enrolled. 5. The patient, and the patient's parent / legal representative where appropriate, and the treating physician agree that the subject will return for all required post-procedure follow up visits and the subject will comply with clinical investigation plan required follow-up visits. Exclusion Criteria: 1. Patient is in need of or has presence of a prosthetic heart valve at any other position 2. Patient has a need for concomitant surgical procedures (non-cardiac) 3. Patients with previously implanted pacemaker (including defibrillators) or mechanical valves 4. Patient has an active bacterial or viral infection or requiring current antibiotic therapy (if temporary illness, patient may be a candidate 4 weeks after discontinuation of antibiotics) 5. Patient has an active endocarditis 6. Leukopenia, according to local laboratory evaluation of white blood cell count 7. Acute or chronic anemia, according to local laboratory evaluation of hemoglobin Patients can be transfused to meet eligibility criteria 8. Thrombocytopenia, defined as Platelet count \< 150,000/mm3 Patients can be transfused to meet eligibility criteria 9. Severe chest wall deformity, which would preclude placement of the PV conduit 10. Known hypersensitivity to anticoagulants and antiplatelet drugs and to the device materials 11. Immunocompromised patient defined as: autoimmune disease, patients receiving immunosuppressant drugs or immune stimulant drugs 12. Patient has chronic inflammatory / autoimmune disease 13. Need for emergency cardiac or vascular surgery or intervention 14. Major or progressive non-cardiac disease (liver failure, renal failure, cancer) that has a life expectancy of less than one year 15. Currently participating, or participated within the last 30 days, in an investigational drug or device study 16. Alcohol or drug abuse as defined by DSM IV-TR criteria for substance abuse - this includes the illicit use of cannabis within the last 12 months 17. Patient has medical, social or psychosocial factors that, in the opinion of the Investigator, could have impact on safety or compliance

Primary outcome measure(s)

  • Freedom from device related death — 1 year
    Percentage of patients that have not died related to the device 1 year from implantation
  • Freedom from Explant — 1 year
    Percentage of patients that have not undergone device explant within 1 year from implantation
  • Freedom from Device-Related Reoperation — 1 year
    Percentage of patients that have not undergone re-operation related to the device within 1 year from implantation
  • Freedom from Device-Related Catheter Intervention — 1 year
    Percentage of patients that have not undergone device related catheter based intervention within 1 year from implantation
  • Freedom from Endocarditis — 1 year
    Percentage of patients that have not had endocarditis within 1 year from implantation
  • Freedom from Thrombus — 1 year
    Percentage of patients that have not had a serious thrombotic event related to the device within 1 year from implantation
  • Freedom from Major Hemorrhage — 1 year
    Percentage of patients that have not had a major bleeding episode related to the device within 1 year from implantation

Trial sites (5)

FacilityCityRegionStatus
OSF Childrens Hospital of Illinois Peoria Illinois Recruiting
Boston Childrens Hospital Boston Massachusetts Recruiting
Cincinnati Children's Hospital Cincinnati Ohio Recruiting
Childrens Hospital of Philadelphia Philadelphia Pennsylvania Recruiting
Childrens Medical Center Dallas Dallas Texas Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05452720 on ClinicalTrials.gov ↗ ← All trials in the USA