An interventional study of Xeltis Pulmonary Valved Conduit in Heart Defects, Congenital, sponsored by Xeltis. Withdrawn at 4 sites in 4 countries. Open to participants aged Up to 21 Years. Per ClinicalTrials.gov, last updated 2021-04-09.
Sponsored by Xeltis · Not applicable, Interventional, and Treatment
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.
Exclusion Criteria:
PV Conduit for RVOT reconstruction
Device: Xeltis Pulmonary Valved Conduit
RVOT reconstruction
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
Plan to share: No
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This study is withdrawn, as verified in Apr 2021. You cannot join it, but the record below documents what was studied.
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Xeltis