LineMatrix® Biological Vascular Graft for the Creation of Arteriovenous Graft

Ki vehet részt

• (1) Age ≥18 years and ≤80 years, male or female
• (2) Diagnosed with end-stage renal disease (ESRD) requiring maintenance hemodialysis
• (3) Requiring establishment of a long-term hemodialysis vascular access but unable to have a autologous arteriovenous fistula (AVF) created
• (4) Assessed by the investigator as suitable for implantation of an arteriovenous graft (AVG) in the upper extremity
• (5) Able to understand the purpose of the study, voluntarily participating and providing signed informed consent(ICF), and willing to comply with all scheduled follow-up assessments

Ki nem vehet részt

• (2) Planned to undergo renal transplantation or transition to peritoneal dialysis within 1 year
• (5) Severe cardiac disease, including New York Heart Association (NYHA) Class III-IV severe heart failure, or history of myocardial infarction, unstable angina, or sustained ventricular tachyarrhythmia requiring continuous treatment within 6 months prior to enrollment
• (6) History of stroke within 1 month prior to enrollment
• (8) Immunodeficiency disorders, or current treatment with corticosteroids (prednisone-equivalent dose ≥10 mg) or immunosuppressive agents (e.g., sirolimus, mycophenolate mofetil, cyclosporine, cyclophosphamide, tacrolimus)
• (19) Currently enrolled in another drug or medical device clinical trial and not yet completed the study
• (1) Known or suspected history of allergy to heparin, alcohol, or bovine-derived products
• (9) Malignancy or other severe systemic disease with a life expectancy of <12 months
• (15) Hypercoagulable state, or history of ≥2 episodes of deep vein thrombosis or peripheral vascular thrombosis not related to dialysis access
• (17) Severe mental disorders that preclude cooperation with the study protocol
• (20) Any other conditions that, in the investigator's opinion, make the patient unsuitable for participation in this clinical trial
• (3) Hemoglobin concentration <60 g/L, or platelet count <60 × 10⁹/L
• (4) Left ventricular ejection fraction (LVEF) <30%
• (7) Uncontrolled or poorly controlled diabetes mellitus (preoperative glycated hemoglobin >10%)
• (11) Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >2 × upper limit of normal (ULN)
• (12) Coagulation disorders (activated partial thromboplastin time [APTT] or prothrombin time [PT] >1.5 × ULN)
• (13) Systemic or surgical site infection (white blood cell [WBC] count >15 × 10⁹/L)
• (10) Heparin-induced thrombocytopenia type II (HIT-2) or other contraindications to heparin use
• (14) Baseline hypotension, or frequent hypotensive episodes within the past month (frequency ≥5 episodes/month, with hypotension defined as systolic blood pressure <90 mmHg or diastolic blood pressure <60 mmHg)
• (16) Known ipsilateral central venous stenosis, or clinical symptoms/signs suggestive of central venous stenosis confirmed by imaging
• (18) Pregnant or lactating women, or women of childbearing potential who plan to conceive during the trial and are unwilling to use effective contraception