About this trial

Multicenter, global, prospective, non-randomized, interventional, post-market trial. All subjects enrolled will receive an Abbott Valved Graft device.

Eligibility criteria

Qualifiers

cardiac surgery including the implant of a VAVGJ or CAVGJ for native or prosthetic valve replacement

Disqualifiers

anticoagulation therapy intolerant

active endocarditis

anatomical or medical, surgical, psychological or social contraindications

Trial design

Treatments tested in this trial

  • VAVGJ
  • CAVGJ

Treatment groups

260 Participants
are divided into 2 treatment groups

Locations

25
Austria
Klinik Floridsdorf1012, Vienna Austria
Denmark
Rigshospitalet2100, Copenhagen Denmark
France
CHU de Besancon - Jean Minjoz25030, Besançon France
CHRU Lille59037, Lille France

Sponsors and collaborators

Abbott Medical Devices

Lead sponsor