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CompletedNCT07436559Updated Aug 4, 2026

AVF Stenosis by Electronic Stethoscope

An observational study in End Stage Renal Disease (ESRD), sponsored by National Taiwan University Hospital. Completed at 1 site in Taiwan. Open to participants aged 20 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-08-04.

Sponsored by National Taiwan University Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
30
Ages
20 Years to 99 Years
Sex
All
01

Study summary

The prevalence rate of hemodialysis in Taiwan is the highest in the world, and the number of new cases of hemodialysis and the death rate are gradually increasing every year. Long-term hemodialysis patients must receive dialysis through the arteriovenous fistula. If the arteriovenous fistula is narrowed, the dialysis effect will be poor or the dialysis will not be possible due to blockage, resulting in complications and mortality. The detection of the arteriovenous fistula must rely on the assistance of professionals.

* Is it easier for clinicians to detect arteriovenous fistula stenosis by an electronic stethoscope?

This study uses an electronic stethoscope to take the hemodialysis center of Douliu District, Yunlin Branch of National Taiwan University Hospital as the experimental site. Select 30 patients who need long-term dialysis, adults (20-99 years old) who have been on dialysis for more than 3 months and have arteriovenous fistula. The experiment period lasted for 3 months, and each person received 2-3 voices per week, about 1080 voices. The main purpose is to use the electronic stethoscope and the experience of traditional professionals, hoping to detect and predict the stenosis in advance. The important key factors of vascular access stenosis in hemodialysis patients were found through regression analysis of the Albumin value and clinical data obtained from routine treatment of patients of a fixed blood test in monthly hemodialysis center.

02

Conditions studied

  • End Stage Renal Disease (ESRD)

Keywords

  • Electronic stethostope
  • Arteriovenous fistula
  • Regression analysis
  • Hemodialysis
03

In context

Kidney Failure, Chronic

2,085 studies on the registry are indexed under Kidney Failure, Chronic; 261 are open to participants now.

This study's enrollment of 30 is below the median of 120 across 431 observational studies indexed under Kidney Failure, Chronic.

Browse Kidney Failure, Chronic studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

End stage renal disease patients received hemodialysis for more than 3 months

Inclusion criteria

  • Age 20-99 years - Chronic hemodialysis ≥3 months - Functional arteriovenous fistula (AVF) - Ability to provide informed consent

Exclusion criteria

Exclusion Criteria:

  • Arteriovenous graft (AVG) - Central venous catheter (Permcath) - Vulnerable populations unable to consent
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
30 participants (actual)
Patient registry
No

Interventions

  • DeviceDetection and Prediction of the stenosis of arteriovenous fistula in hemodialysis patients by an electronic stethoscope

    The detection of the arteriovenous fistula must rely on the assistance of professionals by palpation or a conventional stethoscope. This study will investigate the detection and prediction of arteriovenous fistula stenosis in hemodialysis patients by an electronic stethoscope.

06

What researchers measure

Primary outcomes

  1. AVF stenosis

    Clinical stenosis: Diagnosed by attending nephrologist based on physical examination abnormalities (high-pitched bruit, pulsatile flow, diminished thrill) - Confirmed by Doppler ultrasound showing \>50% diameter reduction - Intervention: Percutaneous transluminal angioplasty (PTA)

    Time frame: From enrollment to the end of study at 3 months

Secondary outcomes

  1. Abnormal AVF sound threshold

    Defined using statistical analysis of post-PTA normal sounds

    Time frame: From enrollment to the end of study at 3 months

07

Study locations

1 site
  • National Taiwan University Hospital Yunlin Branch
    Douliu, Taiwan 640, Taiwan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07436559
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Feb 27, 2026
Start date
Mar 17, 2023
Primary completion
Jun 16, 2023
Completion
Sep 30, 2023
Last update
Aug 4, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2023. You cannot join it, but the record below documents what was studied.

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