the Aorta Arch Stent Graft System Combined With the Endovascular Needle System in Situ Fenestration

LifeTech Scientific

Status

Active, not recruiting

Conditions

Aortic Dissection

Treatments

Device: the Aorta Arch Stent Graft System combined with the Endovascular Needle System

Study type

Interventional

Funder types

Industry

Identifiers

NCT05126446

LTP86-01

Details and patient eligibility

About

A prospective, multi-center, single-group target value method to evaluate the safety and effectiveness of the Aorta Arch Stent Graft System combined with the Endovascular Needle System in situ fenestration technology in the treatment of aortic dissection involving the aortic arch

Full description

Clinical trials using prospective, multi-center, single-group target value design;
120 subjects with aortic dissection requiring partial arch reconstruction will be enrolled in more than 30 centers in China, and they will meet the test enrollment requirements.
CTA examination was performed at baseline, 30 days, 6 months, 12 months, 36 months, and 60 months after surgery to determine the pathological status and the status of postoperative aortic and branch revascularization

Enrollment

120 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria (to be selected if all of the following criteria are met)：

18 years old ≤age≤80 years old, no gender limitation;
Diagnosis of aortic dissection and reconstruction of the left subclavian artery;
The main branches and branches of the aortic arch at the lesion site have sufficient anatomical basis:
- The diameter range of the near-end anchoring zone of the main body of the fixed mechanism: 21-46mm;
- The length of the anchor zone near the principal part of the tunnel is ≥10mm;
- The length of the anchor zone of the branching vessel of the convex target is ≥15mm;
- The diameter range of the distal anchoring zone of the target branching vessel is 5-18mm.
The patient has adequate surgical access vessels;
Patients who understand the purpose of the study, voluntarily participate in and sign informed consent, and are willing to follow up.

Exclusion Criteria (If one of the following criteria is met, it will not be selected)：

The patient is pregnant or breastfeeding;
The patient had a history of cardiac surgery (congenital heart disease surgery, heart valve surgery, coronary heart disease surgery, thoracic aortic surgery, etc.), which would affect the implementation of this TEVAR surgery;
The patient has been implanted or planned to be implanted with left ventricular auxiliary pump, interventional valve and other instruments, or is planning to undergo coronary intervention surgery, and aortic dissection is expected to affect the function of such instruments or such instruments will affect the operation of aortic dissection;
Patients with severe hematoma on the aortic wall in the proximal anchoring area of the stent;
Marfan syndrome and other connective tissue diseases, arteritis;
Patients with a history of allergy to contrast agents, anesthetics, antiplatelet drugs, anticoagulants, nickel peptide alloys, and polytetrafluoroethylene materials;
Patients with a history of cerebral infarction or myocardial infarction within 3 months before surgery;
Patients with active bleeding and coagulopathy;
Abnormal renal function: patients with preoperative creatinine > 2.5 times the normal upper limit value;
Abnormal liver function: patients with alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 5 times the normal upper limit value, or patients with serum total bilirubin (STB) > 2 times the normal upper limit value;
Patients with end-stage diseases with a life expectancy of less than one year;
patients with poor compliance considered by the investigator;
Patients participating in other clinical trials at the same time.