ENDOBARC-S Study: Endovascular Branched Stent-grafts for Aortic ARCh Pathologies in Spain

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The ENDOBARC-S post-market clinical follow-up study is undertaken to evaluate the prevention of death related to aortic arch pathologies when treated by branch stent graft systems (Nexus stent-graft system®, Relay Branch® or Zenith arch branch graft®), with proximal landing at zone 0. The secondary objective is to evaluate the safety and clinical performance of the studied devices.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Patient is between 18 and 90 years old

• Patient with aortic arch pathologies (aneurysm, pseudoaneurysm, dissection, penetrating ulcer, intramural hematoma), treated by branched stent-grafts (Nexus stent graft system©, Relay® Branch or Zenith arch branch graft®, with proximal landing at zone 0.

• Patient must be available for the appropriate follow-up times for the duration of the study

• Informed consent signed.

Locations
Other Locations
Spain
Spanish society for Angiology and Vascular Surgery
RECRUITING
Madrid
Time Frame
Start Date: 2022-01-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 100
Treatments
Patients with aortic arch pathologies treated by branch stent graft systems
Patients with aortic arch pathologies treated by branch stent graft systems (Nexus stent-graft system®, Relay Branch® or Zenith arch branch graft®), with proximal landing at zone 0.
Sponsors
Leads: Vascular Investigation Network Spanish Society for Angiology and Vascular Surgery

This content was sourced from clinicaltrials.gov