Trial Comparing the Incidence of Steal Syndrome in the Two Types of anTEcubitaL Fossa Arteriovenous fistuLa AVF (STEAL)
Primary Purpose
Arteriovenous Fistulas, Renal Failure, End-Stage, Steal Syndrome
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Proximal radial/ulnar artery as inflow
Sponsored by
About this trial
This is an interventional prevention trial for Arteriovenous Fistulas
Eligibility Criteria
Inclusion Criteria:
End stage renal failure Requiring AVF at in the antecubital fossa for haemodialysis
Exclusion Criteria:
When the participant has not received the allocated intervention due to anatomical anomaly, technical issue or any other reason
Sites / Locations
- Addenbrooke's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Brachial artery inflow
Proximal radial/ulnar artery as inflow
Arm Description
Elbow fistula created with brachial artery as inflow (ie. either brachiocephalic or brachiobasilic fistulas)
Elbow fistula created with either proximal radial or ulnar artery as inflow
Outcomes
Primary Outcome Measures
Incidence of steal syndrome as measured by Hoek Score
Determine the incidence of steal syndrome in the 2 arms of the study
Secondary Outcome Measures
Presence of severe steal syndrome necessitating surgical revision/ligation
Determine the presence of severe steal syndrome necessitating surgical revision/ligation
Operative time
Determine the efficacy of the two study interventions in terms of operative time.
Utilisation of fistula
Determine the efficacy of the two study interventions in terms of utilisation.
Full Information
NCT ID
NCT02297451
First Posted
October 29, 2014
Last Updated
January 7, 2020
Sponsor
Cambridge University Hospitals NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT02297451
Brief Title
Trial Comparing the Incidence of Steal Syndrome in the Two Types of anTEcubitaL Fossa Arteriovenous fistuLa AVF
Acronym
STEAL
Official Title
Randomised Controlled Trial Comparing the Incidence of Steal Syndrome in the Two Types of anTEcubitaL Fossa Arteriovenous fistuLa AVF (STEAL Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cambridge University Hospitals NHS Foundation Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background:
Arteriovenous fistula (AVF) is a form of vascular access for haemodialysis. An AVF is normally created at the level of the wrist, but occasionally it is created in the elbow when there is no suitable vessel in the forearm. The most common type of elbow (antecubital) fistula (AFF) is a brachiocephalic fistula, which carries significantly higher risk of steal syndrome (AVF-associated hand ischaemia) than wrist fistulas. More recently, AFF using proximal radial or ulnar artery as inflow has been described and shown to have a lower rate of Steal syndrome than brachiocephalic fistula. This study aims to investigate the incidence of steal syndrome between AFF using brachial artery and that using the proximal radial/ulnar artery as inflow.
Detailed Description
Arteriovenous fistulas (AVF) are the safest form of vascular access for long-term haemodialysis in patients with end-stage renal failure. The strategy in creating an AVF in the upper limbs is to start at a distal site and if that fails, to attempt an AVF on a more proximal site i.e. from wrist, forearm to elbow. The most common type of AVF is the radiocephalic AVF at the wrist. A more proximal AVF is often created as a primary procedure when there is poor vasculature in the distal forearm or as a secondary procedure when a wrist fistula has failed. Traditionally, brachiocephalic fistulas (BCF), which involves anastomosing the cephalic vein to the brachial artery, have been the most common type of AVF created in the antecubital fossa at the elbow level. Other common types of antecubital fossa arteriovenous fistula (AFF) are the brachiobasilic (BBF) and brachio-median cubital AVF.
Steal syndrome relates to hand ischaemia associated with AVF creation, and is a major risk of AVF formation. The symptoms of steal syndrome ranges from cold extremities, numbness, hand claudication (pain after exercise), to rest pain and tissue loss. Steal syndrome can also be measured by Digital Brachial Pressure Index. Severe steal syndrome is debilitating, and limb-threatening, and requires surgical revision or ligation of the AVF. This leads to additional surgical risks and loss of dialysis vascular access.
Diabetes and the types of AVF have been found to be independent risk factors for developing steal syndrome following AVF creation1. The highest risk is seen in patients with a proximal AVF i.e. BCF/BBF; up to 50% of patients in some studies, compared to 5-8% in all upper limb AVFs.
An alternative technique that may reduce risk of steal in this group of patients is to anastomose the vein to the radial artery or ulnar artery, distal to the brachial artery bifurcation. This technique, theoretically, will only 'steal' blood from one artery e.g. radial artery if the anastomosis is created on the proximal radial artery so blood flow can therefore be maintained by the ulnar arterial system.
Recent studies have suggested that using the proximal radial or ulnar artery reduced the risk of steal to as low as 0% to 3%. The type of arterial inflow to an AFF is therefore a potentially significant factor in causing steal syndrome. There is, however, no current randomised controlled trial to prove this hypothesis.
The definition of steal syndrome varies greatly in the literature. Some studies have defined steal syndrome as the presence of mild symptoms such as cold hand, while the others reported steal syndrome when it was severe enough to require surgical intervention. This has led to the huge variations in the incidence of steal syndrome being reported and has made comparison difficult between studies. A few scoring systems to describe the severity of steal syndrome have been suggested in previous studies, but none of them has been widely used.
In this study, the difference in the severity of steal between the two intervention groups will be investigated. This will be done using the Hoek score, which was originally used by Hoek et al in 2006 to report steal syndrome associated with the AVFs created in their centre. There was, however, no comparison of scores among the different types of AVF.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arteriovenous Fistulas, Renal Failure, End-Stage, Steal Syndrome
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
79 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Brachial artery inflow
Arm Type
No Intervention
Arm Description
Elbow fistula created with brachial artery as inflow (ie. either brachiocephalic or brachiobasilic fistulas)
Arm Title
Proximal radial/ulnar artery as inflow
Arm Type
Active Comparator
Arm Description
Elbow fistula created with either proximal radial or ulnar artery as inflow
Intervention Type
Procedure
Intervention Name(s)
Proximal radial/ulnar artery as inflow
Intervention Description
Proximal radial/ulnar artery used as inflow
Primary Outcome Measure Information:
Title
Incidence of steal syndrome as measured by Hoek Score
Description
Determine the incidence of steal syndrome in the 2 arms of the study
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Presence of severe steal syndrome necessitating surgical revision/ligation
Description
Determine the presence of severe steal syndrome necessitating surgical revision/ligation
Time Frame
6 months
Title
Operative time
Description
Determine the efficacy of the two study interventions in terms of operative time.
Time Frame
6 months
Title
Utilisation of fistula
Description
Determine the efficacy of the two study interventions in terms of utilisation.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
End stage renal failure Requiring AVF at in the antecubital fossa for haemodialysis
Exclusion Criteria:
When the participant has not received the allocated intervention due to anatomical anomaly, technical issue or any other reason
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gavin Pettigrew, MD, FRCS
Organizational Affiliation
University of Cambridge
Official's Role
Principal Investigator
Facility Information:
Facility Name
Addenbrooke's Hospital
City
Cambridge
ZIP/Postal Code
CB2 0QQ
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
Trial Comparing the Incidence of Steal Syndrome in the Two Types of anTEcubitaL Fossa Arteriovenous fistuLa AVF
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