About this trial
The primary objective of this study is to evaluate the safety and efficacy of the TEVAR combined with extended bare-metal stenting (distal landing zone ≥2 cm below renal arteries) in patients with acute complicated type B aortic dissection (ATBAD).
Additionally, to prevent postoperative true lumen hypoperfusion in residual thoracoabdominal aortic dissection (visceral zone, infrarenal aorta, and iliac arteries) and persistent ischemic manifestations in visceral and lower extremity arteries post-endovascular repair, extended bare-metal stents are deployed to maintain adequate distal true lumen patency. This strategy ensures perfusion to visceral branches and lower limbs while preparing for future complete endovascular aortic repair.
Eligibility criteria
Qualifiers
≧18 years old, ≦80 years old;
Acute phase with a course of disease ≦14 days;
CTA confirmed diagnosis of active dissection type B in accordance with the Stanford classification in the ESC guidelines, and requiring TEVAR surgery;
For patients with acute non-type A and non-type B aortic dissection involving the left subclavian artery: current technologies (such as fenestration, single branch, chimney, etc.) can be used to solve the reconstruction of the left subclavian artery;
Disqualifiers
Dissection termination above renal arteries;
Major aortic surgery within 30 days prior (except LSA revascularization);
Iliofemoral stenosis/angulation precluding endovascular access;
Non-diagnostic CTA image quality;
Trial design
Treatments tested in this trial
- Hybrid TEVAR combined with long bare-metal stent intervention