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Clinical Trials/ISRCTN36033877
ISRCTN36033877
Completed
未知

A prospective observational cohort study to determine whether ultrasound surveillance can reliably predict arteriovenous fistulae failure in patients with chronic kidney disease

Cambridge University Hospitals NHS Foundation Trust and University of Cambridge0 sites348 target enrollmentAugust 9, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Arteriovenous fistula in patients with established or approaching end stage renal disease (ESRD) requiring dialysis
Sponsor
Cambridge University Hospitals NHS Foundation Trust and University of Cambridge
Enrollment
348
Status
Completed
Last Updated
last year

Overview

Brief Summary

2019 Protocol article in https://pubmed.ncbi.nlm.nih.gov/31340975/ protocol (added 07/08/2020) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33796281/ (added 21/09/2023) 2024 Results article in https://doi.org/10.1016/j.ekir.2024.01.011 (added 25/04/2024) 2024 Results article in https://pubmed.ncbi.nlm.nih.gov/38768043/ (added 22/05/2024)

Registry
who.int
Start Date
August 9, 2018
End Date
January 31, 2020
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Cambridge University Hospitals NHS Foundation Trust and University of Cambridge

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged 16 years or older
  • 2\. End stage renal disease
  • 3\. Requires haemodialysis or is likely to do so immediately
  • 4\. Due creation of an arm arteriovenous fistula (wrist or elbow), including the following types of fistula with a minimal acceptable threshold of 2 mm venous diameter at whatever site chosen:
  • 4\.1\. Radiocephalic
  • 4\.2\. Ulno\-basilic
  • 4\.3\. Brachiocephalic
  • 4\.4\. Brachiobasilic
  • 5\. Provides fully informed consent

Exclusion Criteria

  • 1\. Attempted formation of proximal neo\-anastomosis at the forearm cephalic and basilic venous systems following failure of a standard radiocephalic or ulnobasilic fistula
  • 2\. Known central venous stenosis (including those who undergo simultaneous central venous angioplasty / stenting and arteriovenous fistula creation)
  • 3\. Anticipated that it will not be possible to perform serial ultrasound scanning

Outcomes

Primary Outcomes

Not specified

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