The Use of Hepatitis C Positive Kidneys in Hepatitis C Negative Kidney Transplant Recipients
- Conditions
- Kidney TransplantationHepatitis C
- Registration Number
- NCT03809533
- Lead Sponsor
- Amit D Tevar, MD
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Active, not recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion criteria (recipients):<br><br> 1. Patients with end-stage renal disease listed for kidney transplantation at UPMC.<br><br> 2. On chronic hemodialysis or peritoneal dialysis or stage 5 chronic kidney disease<br> (CKD) defined as a glomerular filtration rate < 15 ml/min<br><br> 3. Age = 18<br><br> 4. No available living kidney donor<br><br> 5. Listed for an isolated kidney transplant at UPMC with <60m of accrued transplant<br> waiting time and/or <60m of dialysis time<br><br> 6. Have panel reactive antibody level of <98%<br><br> 7. No obvious contraindication to kidney transplant<br><br> 8. Able to travel to UPMC for routine post-transplant visits and study visits for a<br> minimum of 12 months after transplantation<br><br> 9. Able to provide informed consent<br><br> 10. Be willing to use a contraceptive method for a year after transplant<br><br>Exclusion criteria (recipients):<br><br> 1. HIV positive<br><br> 2. HCVAb or HCV RNA positive<br><br> 3. Presence of behavioral risk factors for contracting HCV other than being on<br> hemodialysis. These behavioral risk factors are current injection drug use, current<br> intranasal illicit drug use, current percutaneous/parenteral exposures in an<br> unregulated setting.<br><br> 4. Hepatitis B surface antigen positive<br><br> 5. History of liver cirrhosis<br><br> 6. Persistently elevated liver transaminases, defined as ALT/AST at least 3 times the<br> upper limit of normal for a minimum of 3 consecutive months<br><br> 7. History of atrial fibrillation requiring the use of amiodarone over the past 12m<br><br> 8. Patients with etiology of renal failure with increased risk of causing early graft<br> failure as assessed by the investigator team<br><br> 9. Receipt of prior organ transplant<br><br> 10. Waitlisted for a multi-organ transplant<br><br> 11. Pregnant women<br><br> 12. Known allergy to sofosbuvir/velpatasvir<br><br> 13. Any condition, psychiatric or physical, that in the opinion of the investigator<br> would make it unsafe to proceed with transplantation or interfere with the ability<br> of the subject to participate in the study<br><br>Inclusion criteria (donors):<br><br> 1. HCV antibody positive<br><br> 2. HCV NAT negative or positive<br><br> 3. Kidney donor profile index (KDPI) score <85<br><br>Exclusion criteria (donors):<br><br> 1. Confirmed HIV positive (positive HIV-1 antibody, positive HIV-2 antibody, positive<br> p24 antigen and/or positive HIV NAT)<br><br> 2. Confirmed HBV positive (positive hepatitis B surface antigen and/or HBV NAT)<br><br> 3. Known ongoing therapy for HCV
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adverse Events;HCV free at 1 year
- Secondary Outcome Measures
Name Time Method Transmission rate of HCV from HCVAb+/NAT- donors to HCVAb- recipients;Incidence of allograft rejection;Incidence of graft loss;All-cause mortality;Waitlist time after enrollment