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Taking people in ItalyNo phase

Studying blood flow and sounds in dialysis access fistulas

Compares blood flow and fistula sounds using MRI and ultrasound in adults with kidney failure.

Plain-language title generated from the registry record
Registry title: Blood Flow Conditions and Sounds in AVFs

Key facts

Where
Bergamo, ItalySee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 90 years old?

Source: NCT06411353, who can take part

Where in Italy

  • A.O. Papa Giovanni XXIII - U.O. Nefrologia e DialisiBergamo, ItalyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Mario Negri Institute for Pharmacological Research
Trial code
NCT06411353
Record updated
4 September 2025
Original description
This is a prospective non-pharmacological interventional study aimed at investigating the relationship between the blood flow condition and the arteriovenous fistula (AVF) sound, with the ultimate aim of predicting the AVF clinical, in patients with end-stage renal disease (ESRD) who require the creation of a vascular access for extracorporeal circulation.Read full original descriptionShow less

The Relationship Between Blood Flow Conditions and Sounds in Arteriovenous Fistulae for Hemodialysis

This is a prospective non-pharmacological interventional study aimed at investigating the relationship between the blood flow condition and the arteriovenous fistula (AVF) sound, with the ultimate aim of predicting the AVF clinical, in patients with end-stage renal disease (ESRD) who require the creation of a vascular access for extracorporeal circulation.

Inclusion: Provision of informed consent prior to any study specific procedures; Female and/or male aged between 18 and 90 years; Patients in HD treatment who need a new VA or patients who entered the pre-dialysis program because of ESRD. In all cases, the first-choice treatment is the surgical creation of an autogenous AVF in patient's forearm.

Exclusion: Presence of a previously failed AVF in the same arm selected for surgery; Patients with contraindications to MRI including: pregnancy, claustrophobia, cardiac pacemakers or other MRI-incompatible prostheses; Contraindications for the creation of an autogenous AVF; Patients already on HD treatment through a catheter or a graft; Patients undergoing peritoneal dialysis; Patients with a life expectancy of less than 2 years.

ClinicalTrials.gov NCT06411353