ClinicalTrials.Veeva

Menu

AVF Volume Blood Flow Reduction in HD Patients

M

Moscow Regional Research and Clinical Institute (MONIKI)

Status

Completed

Conditions

Heart Failure
Chronic Kidney Disease Stage 5

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Heart failure with preserved / high cardiac output is a well-known syndrome in patients with high-flow arteriovenous fistula (AVF). However, the threshold for classifying an AVF as high-flow is currently undefined. Cardio-fistular recirculation (CFR) is often used as a criterion, with values greater than 25-30% considered cardiotoxic and associated with adverse outcomes. Additionally, CFR is one of the few easily modifiable risk factors through surgical reduction of AVF volume blood flow (Qa).

The study aimed to evaluate the extent of involution of heart structural and functional changes following Qa reduction in patients with heart failure and CFR > 25%.

Enrollment

86 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent
  • age > 18 years
  • CKD 5D
  • Native arteriovenous fistula or vascular graft
  • Heart failure with preserved CO (NYHA I-IV )
  • Cardio-fistula recirculation ≥ 25%
  • eKt/V > 1.2
  • Absence of arrhythmias (except grade I AV block)
  • Absence of valvular disease (except mitral regurgitation I-II)
  • Arteriovenous fistula blood flow reduction surgery

Exclusion criteria

  • Death
  • Kidney transplantation
  • Conversion of vascular access to central venous catheter
  • Withdrawal of informed consent

Trial design

86 participants in 2 patient groups

NYHA I-II
Description:
Patients with NYHA I-II heart failure
NYHA III-IV
Description:
Patients with NYHA III-IV heart failure

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems