First Affiliated Hospital Xi'an Jiaotong University
Phase
Observational
Started
2018-06-01
Last updated
2023-07-28
Condition(s) studied
Acute Aortic Syndrome
Investigational drug(s) / intervention(s)
the Castor single branch stent graft
the Castor single branch stent graft: Participants who received thoracic endovascular aortic repair by meant of the Castor single branch stent graft from June 2018 to June 2022 were enrolled in our study.
Study summary
The objective of this study to evaluate the safety and effectiveness of the Castor single branch stent graft for endovascular repair of acute aortic syndrome patients without an inadequate proximal landing zone (\<15mm)
Eligibility
Sex
ALL
Min age
18 Years
Max age
95 Years
Healthy volunteers
No
Inclusion Criteria:
* Patients with acute Stanford type B aortic syndrome who received thoracic endovascular aortic repair by meant of Castor single branch stent graft from June 2018 to June 2022
Exclusion Criteria:
* Patients with acute type B aortic syndrome with an adequate proximal landing zone (≥15mm)
* Previous endovascular repair of the aorta
* Patients with missing data and loss of follow-up
Primary outcome measure(s)
Immediate post-operative technique success — immediately post operation Immediate technical success is defined as successful delivery of the aortic and branching stent graft conveyors to their predetermined position, accurate positioning and successful deployment of the stent, safe removal of the delivery device outside the body, absence of Type I and III endoleaks on angiography at the end of the procedure, and patent branch stents.
All-cause mortality and major — 1-year post operation All-cause mortality includes aortic mortality, non-aortic mortality, and mortality from unknown causes.
Trial sites (1)
Facility
City
Region
Status
First Affiliated Hospital of Xi'an Jiaotong University
Xi'an
Shaanxi
Recruiting
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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