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Evaluation of modified no-touch technique for long-term outcomes of arteriovenous fistulas: A Single-center, Randomized Controlled Trial

Evaluation of modified no-touch technique for long-term outcomes of arteriovenous fistulas: A Single-center, Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068320
Enrollment
Unknown
Registered
2023-02-15
Start date
2023-02-15
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

arteriovenous fistula

Interventions

Experimental group:Modified no-touch technique
Control group:traditional anastomosis technique

Sponsors

Suzhou Science and Technology City Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients who need to establish autologous arteriovenous fistula and are willing to participate in this study; 2. No surgical contraindications; 3. The inner diameter of the cephalic vein is >= 2 mm, and the radial artery is >= 1.6 mm. Ultrasonography evaluates the patient without stenosis and thrombosis in the outflow tract vein and artery on the operating side.

Exclusion criteria

Exclusion criteria: ? Patients who do not agree to participate in this study; ? Unable to follow the procedures specified in this study; ? Those who have contraindications and are not suitable for the operation of autologous internal fistula; ? The diameter of the cephalic vein at the site of the upper limb to be anastomosed on the surgical side is less than 2mm, and the radial artery is less than 1.6mm.

Design outcomes

Primary

MeasureTime frame
Inner diameter of outflow vein at 1.5 cm near anastomosis;Secondary patency rate;

Secondary

MeasureTime frame
haemodynamics;Primary patency rate;

Countries

China

Contacts

Public ContactHou Guocun

Suzhou Science and Technology City Hospital

houguocun2007@163.com19951296331

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026