Skip to content

Influence of two local anaesthetic techniques on the survival of arteriovenous fistulas created for renal dialysis access

Influence of local and regional anaesthetic techniques on arteriovenous fistula access survival - a randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN39571402
Enrollment
220
Registered
2012-01-18
Start date
2012-01-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Surgical arteriovenous fistula for renal access dialysis Nutritional, Metabolic, Endocrine Dependence on renal dialysis

Interventions

We are comparing two well established approaches to the creation of arteriovenous fistulas for renal access dialysis: 1. Arteriovenous fistula created under regional axillary block using levobupivaca

Sponsors

City Hospitals Sunderland NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients referred for creation of a new radiocephalic or brachiocephalic fistula who consent to take part in the study and agree to have the procedure performed while conscious. 2. Aged 18 - 90 3. Male and female participants

Exclusion criteria

Exclusion criteria: 1. Patients who require revision surgery. 2. Having had previous arteriovenous fistula surgery is not a contraindication to recruitment provided the new procedure is not revision surgery 3. Patients undergoing the procedure under General Anaesthetic 4. Known allergy to levobupivacaine (extremely rare)

Design outcomes

Primary

MeasureTime frame
Fistula Doppler flow rate measurement at eight weeks post operatively. This measurement is already performed on all arteriovenous fistulas as part of routine arteriovenous fistula management.

Secondary

MeasureTime frame
1. A patient satisfaction survey pertaining to patient experience of the local/regional anaesthetic techniques, the surgical procedure and their overall hospital experience will be undertaken 2. A standardized and validated questionnaire using a 5-point Likert scale will be provided to patients following the procedure and we will ask them to complete it before they leave hospital

Countries

United Kingdom

Outcome results

None listed

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