Exploratory Research of PCSK9 Inhibitor on Patency of aAVF After PTA With PCB

Last updated: September 10, 2023
Sponsor: RenJi Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

pcsk9 inhibitor

Clinical Study ID

NCT06034691
LY2023-113-A
  • Ages 17-76
  • All Genders

Study Summary

Autologous arteriovenous fistula (AVF) is the preferred vascular pathway type for maintenance hemodialysis (MHD) patients. The K/DOQI guidelines suggest that the use of percutaneous transluminal angioplasty (PTA) as the primary treatment for AVF stenosis is reasonable. However, the durability of PTA is limited. In order to reduce the risk of dysfunction recurrence after the intervention, there have been reports in recent years that drug-coated balloons (DCB) are used in the treatment of vascular stenosis in hemodialysis. Multiple factors have limited the efficacy of DCB. Previous studies on the related factors of hemodialysis access stenosis showed that Dyslipidemia was significantly related to the short initial patency rate, and Dyslipidemia was an important predictor of secondary patency loss. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are a new type of lipid-lowering drug that can prevent vascular calcification. Previous studies have shown that PCSK9 inhibitors have good lipid-lowering effects in both MHD patients and nondialysis patients, and the use of PSK9 inhibitors at the same dose as nondialysis patients is safe in MHD patients. There are currently few studies on the use of paclitaxel-releasing balloon dilation combined with PCSK9 inhibitors to improve autologous internal fistula. Therefore, the investigators applied a prospective, randomized, and controlled study method to preliminarily explore the effect of paclitaxel releasing balloon combined with PCSK9 inhibitor on improving the postoperative patency rate of AVF and the safety of the combined application.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Agree to join this study and sign an informed consent form
  2. Age ≥ 18 years old and ≤ 75 years old, regardless of gender
  3. Maintenance hemodialysis patients using autologous arteriovenous fistula (AVF), with adialysis frequency of three times a week
  4. AVF venous stenosis: The local stenosis rate exceeds 50% of the normal diameter ofnearby blood vessels and is accompanied by at least one of the following conditions:
  5. The natural blood flow of the internal fistula is less than 500ml/min or hasdecreased by more than 25% compared to the previous examination result
  6. Unable to meet the required blood flow for dialysis prescription (bloodflow<200ml/min, and cannot be corrected after adjusting the puncture needleposition)
  7. Decreased arterial pressure or increased venous pressure during dialysis (monitoring arterial pressure<-120mmHg for more than 2 consecutive times ormonitoring venous pressure>120mmHg while maintaining 200ml/min blood flow)
  8. Difficulty in puncture: A qualified nurse who has difficulty puncturing for 3consecutive days of hemodialysis (blood can only be drawn out after more than twopunctures)
  9. Decreased dialysis adequacy [arteriovenous fistula recirculation rate (RA)>10%,or an increase of more than 25% compared to the previous examination result] [RA=(SA-A)/(SA-V) * 100, dialysis to 1 hour: SA=blood flow adjusted to 20ml/min,ultrafiltration and dialysate flow stopped, after 2 minutes, artery Blood ureanitrogen concentration A=artery Blood urea nitrogen concentration V=vein Bloodurea nitrogen concentration]
  10. Abnormal signs of fistula.
  11. Patients with primary Hypercholesterolemia [LDL-C ≥ 130 mg/dl (≥ 3.4 mmol/L), and/ornon-HDL-C≥ 160 mg/dl (≥ 4.1 mmol/L)] or combine cardiovascular disease or assesspatients with a high risk of cardiovascular disease

Exclusion

Exclusion Criteria:

  1. MHD with AVG
  2. Breastfeeding or Pregnant Women
  3. Patients with central venous reflux obstruction
  4. Patients with AVF feeding artery disease
  5. Patients with severe Hypotension (systolic blood pressure<90mmHg or diastolic bloodpressure<60mmHg, at least three times within one month before signing the informedconsent)
  6. Left ventricular Ejection fraction less than 30% or hemodynamic instability
  7. Patients receiving immunotherapy or suspected/confirmed Vasculitis
  8. Patients with coagulation dysfunction or a history of Thrombocytopenic purpura
  9. Patients with vascular access infections or systemic active infections
  10. Patients who are known to be allergic to PCSK9 inhibitors or paclitaxel
  11. Patient's life expectancy is less than 12 months
  12. Patients who are planning kidney transplantation or switching to Peritoneal dialysis
  13. Patients participating in other intervention studies
  14. The researcher judged that the subject's condition was not suitable for participationin this study

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: pcsk9 inhibitor
Phase:
Study Start date:
September 10, 2023
Estimated Completion Date:
October 01, 2024

Connect with a study center

  • Yuanyuan Xie

    Shanghai, Pudong 200127
    China

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.