Actively Recruiting
Safety and Efficacy of XJ-Procedure in Patients With Acute Type A Aortic Dissection Surgery
Led by First Affiliated Hospital Xi'an Jiaotong University · Updated on 2024-07-12
680
Participants Needed
1
Research Sites
202 weeks
Total Duration
On this page
Sponsors
F
First Affiliated Hospital Xi'an Jiaotong University
Lead Sponsor
Z
Zhejiang Provincial People's Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a national, multicenter, open-label, randomized, controlled, endpoint-blinded clinical trial of patients diagnosed with ATAAD and undergoing "Sun's procedure" coordinated by the First Affiliated Hospital of Xi'an Jiaotong University, China. Per the protocol, "Sun's procedure" combined with "XJ-Procedure" in the anastomosis of the aortic root and Sun's procedure combined with regular suturing methods of the aortic root will be compared.
CONDITIONS
Official Title
Safety and Efficacy of XJ-Procedure in Patients With Acute Type A Aortic Dissection Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-70 years
- Patients diagnosed with acute type A aortic dissection (ATAAD) who need Sun's procedure as assessed by a clinician
You will not qualify if you...
- Severe aortic root involvement such as root diameter greater than 45 mm, root tear, severe destruction of the aortic root, or combined valve disease
- Combined coronary artery disease requiring coronary revascularization
- Previous aortic or cardiac surgery
- Severe preoperative malperfusion syndromes including serious cerebral complications or abdominal organ/lower extremity malperfusion lasting more than 12 hours
- Severe single or multiple organ failure before surgery
- Pregnant women
- Refusal to sign informed consent or participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
First Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, China, 710061
Actively Recruiting
Research Team
Y
Yang Yan
CONTACT
G
Guoliang Li
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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