Arteriovenous fistula anastomosis in patients with chronic renal failure

Comparison of proximal arteriovenous fistula anastomosis side by side to end in patients with chronic renal failure

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190717044255N6

Enrollment

Registered

2022-09-03

Start date

2022-09-23

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

Chronic renal failure. Hypertensive heart and chronic kidney disease without heart failure, with stage 5 chronic kidney disease, or end stage renal disease

Interventions

Intervention 1: First intervention group: In the first group, arteriovenous anastomosis will be performed in 36 patients who are candidates for arteriovenous fistula with the technique of connecting t

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Arteriovenous fistula candidate patients

Exclusion criteria

Exclusion criteria: Hepatic disease pregnancy

Design outcomes

Primary

Measure	Time frame
Bleeding. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Physical examination.;Maturation of fistula. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Physical examination.;Pain at the fistula site. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Visual Analogue Scale of pain.;Thrombosis. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Physical examination.	—

Measure

Time frame

Bleeding. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Physical examination.;Maturation of fistula. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Physical examination.;Pain at the fistula site. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Visual Analogue Scale of pain.;Thrombosis. Timepoint: After surgery and every two weeks until the maturity of the fistula. Method of measurement: Physical examination.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDarioush Poorakpour

Arak University of Medical Sciences

drpoorakpour1988@gmail.com+98 86 3313 6505

Outcome results

None listed

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