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Reliability, complications and outcome of conductive arteriovenous fistula compared to conventional non-conductive arteriovenous antecubital fistula in patients referred for AVF construction at Tabriz Imam Reza Hospital in 2012-2013

Reliability, complications and outcome of conductive arteriovenous fistula compared to conventional non-conductive arteriovenous antecubital fistula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015040716473N4
Enrollment
100
Registered
2015-04-16
Start date
2013-01-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic Kidney Disease. Chronic kidney disease, stage 5

Interventions

Intervention 1: AVF reconstruction between the brachial artery and cephalic vein. Intervention 2: AVF reconstruction between the brachial artery and basilic or communicating vein.
Treatment - Surgery
AVF reconstruction between the brachial artery and cephalic vein
AVF reconstruction between the brachial artery and basilic or communicating vein

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients with chronic renal failure which referred for arteriovenous fistula (AVF) reconstruction as an access route for dialysis; age over 12Y/O;possibility of AVF reconstruction in the antecubital fossa; presence of both basilic and cephalic vein with a communicating vein between them; no significant brachial artery stenosis; no preoperative distal ischemia; no recent venous needling in the antecubital fossa. Exclusion criteria:any contraindication for AVF reconstruction in antecubital fossa; presence of a good forearm radial artery and cephalic vein for distal AVF reconstruction; absence of a communicating antecubital vein; absence of basilic or cephalic vein in the antecubital fossa; fibrosis of the antecubital or arm veins; no palpable thrill during irrigation of the antecubital veins with heparinized saline

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dialysability. Timepoint: 2 months after the operation. Method of measurement: by the dialysis nurse.

Secondary

MeasureTime frame
Arterial steal syndrome. Timepoint: any time during 2 months after the operation or after the first dialysis session. Method of measurement: diagnosis by the attending physician or dialysis nurse.;Venous hypertension syndrome. Timepoint: any time during the first 2 months the operation or after the first session of dialysis. Method of measurement: measurment of forearm circumference by attending physician or dialysis nurse.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBassir Abolghasemi Fakhri

Tabriz University of medical sciences

bfakhree@yahoo.com+98 41 3334 1317

Outcome results

None listed

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