This is a multi-center prospective, single-arm, non-randomized, open label study to assess safety and performance of the Xeltis Pulmonary Valved Conduit in subjects requiring Right Ventricular Outflow Tract correction or reconstruction due to congenital heart malformations.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
RVOT reconstruction
Gottsegen György Hungarian Institute of Cardiology, Paediatric Cardiac Centre
Budapest, Hungary
Institute Jantung Negara, National Heart Institute
Kuala Lumpur, Malaysia
University Children's Hospital of Cracow (UCH),
Krakow, Poland
Childrens Heart Centre Slovak Republic
Bratislava, Slovakia
Survival at 12 months follow up post implantation
Measured by the fact that the patient is still alive at the time of the 12 month FU visit
Time frame: 12 months
Freedom from device related death, intervention and/or reoperation at 12 months follow up
Measured by the fact that the patient did not die, did not have a reoperation or reintervention during the first 12 months
Time frame: 12 months
Mean pressure gradient across the area of conduit implantation (RV to PA) of less than 40 mm Hg at 12 months follow up
Time frame: 12 months
Pulmonary regurgitation of equal or less than moderate (≤40 %) at 12 months follow up
Time frame: 12 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.