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Evaluation of the effectiveness of modified side-to-side anastomosis versus end-to-side anastomosis for the creation of arteriovenous internal fistula

Evaluation of the effectiveness of modified side-to-side anastomosis versus end-to-side anastomosis for the creation of arteriovenous internal fistula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050186
Enrollment
Unknown
Registered
2021-08-21
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

hemodialysis

Interventions

experimental group:modified side-to-side anastomosis
control group:End-side anastomosis

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 80 years; 2. Upper extremity autogenous arteriovenous fistula (forearm radio-cephalic, ulno-basilic, proximal brachio-cephalic or brachio-basilic configurations); 3. Vascular ultrasound arterial diameter >= 2 mm and venous diameter >= 2.5 mm within 1 week prior to surgery.

Exclusion criteria

Exclusion criteria: 1. No upper extremity arteriovenous ultrasound within 1 week prior to surgery; 2. Missed visits during the follow-up period.

Design outcomes

Primary

MeasureTime frame
maturation rate of arteriovenous fistula;—

Countries

China

Contacts

Public ContactCui Tianlei

West China Hospital, Sichuan University

tianleicui@163.com+86 18980601979

Outcome results

None listed

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