About this trial

Multi-arm, multi-center, open label, prospective observational registry designed to obtain safety and performance data on the use of CE marked and custom Terumo Aortic endovascular grafts.

Eligibility criteria

Qualifiers

Minimum age as per local regulations

Indication for aortic endovascular repair with an approved or CE marked by a Regulatory body or custom-made Terumo Aortic Endovascular graft

Ability to provide informed consent

Willingness to comply with the registry protocol

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Thoracic
  • Abdominal
  • Custom Device
  • Illiac Artery

Treatment groups

1,000 Participants
are divided into 4 treatment groups

Locations

58
Belgium
Imeldaziekenhuis Bonheiden Belgium
Clinques Uni. St Lucs Brussels Belgium
France
Hôpital Pneumologique et Cardiovasculaire Louis-Pradel Bron France
CHU St Etienne Saint-Etienne France

Sponsors and collaborators

Vascutek Ltd.

Lead sponsor

Bolton Medical

Collaborator