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Evaluation of the Radial Artery Deviation And Reimplantation Technique for Primary Hemodialysis Access Creation (RADAR)

Primary Purpose

End-stage Renal Disease

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
End-cephalic vein to side-radial artery fistula creation
RADAR fistula creation
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-stage Renal Disease focused on measuring Vascular access, Hemodialysis, Arteriovenous fistula, Stenosis, Failure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient referred by the nephrologist for the creation of a primary vascular access
  • Clinical examination of both upper limbs showing on the same limb:

    • A cephalic vein at the distal third of the forearm
    • Radial pulse
    • Ulnar pulse
    • Positive Allen test (patent palmar arches)
  • Preoperative arterial and venous duplex ultrasound examination of both limbs showing on the same limb :

    • A patent cephalic vein, ≥2mm in diameter at the distal 1/3 of the forearm, free from stenosis, ≥15cm in length
    • A patent on dominant radial artery, ≥2mm in diameter at the distal 1/3 of the forearm, free from stenosis and major calcifications
    • A patent ulnar artery, free from stenosis and major calcifications
    • A positive Allen's test with assessment of the retrograde flow (patent palmar aches)
  • Digital pressure >50mmHg when occlusive compression is made on the radial artery and digital/brachial ratio >0.5

Exclusion Criteria:

  • patient under guardianship

Sites / Locations

  • CHU de Nice - Service de chirurgie vasculaireRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

arteriovenous fistula (AVF)

RADAR

Arm Description

Patient receiving a traditional arteriovenous fistula at the wrist (end-cephalic vein to side-radial artery)

Patient receiving an arteriovenous fistula at the wrist using the Radial Artery Deviation And Reimplantation technique (end-radial artery to side-cephalic vein)

Outcomes

Primary Outcome Measures

Primary patency rate of the access

Secondary Outcome Measures

Assisted primary patency rate of the access

Full Information

First Posted
March 31, 2016
Last Updated
August 14, 2019
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT02728817
Brief Title
Evaluation of the Radial Artery Deviation And Reimplantation Technique for Primary Hemodialysis Access Creation
Acronym
RADAR
Official Title
Evaluation of the Radial Artery Deviation And Reimplantation Technique for Primary Hemodialysis Access Creation: a Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Unknown status
Study Start Date
April 12, 2017 (Actual)
Primary Completion Date
April 12, 2021 (Anticipated)
Study Completion Date
May 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The Radial Artery Deviation And Reimplantation (RADAR) technique is a new approach for the construction of hemodialysis arteriovenous fistula. In this technique, the radial artery pedicle is deviated towards the minimally dissected cephalic vein at the wrist. The aim of this study is to compare the safety and efficacy of this technique with the traditional end-cephalic to side-radial arteriovenous fistula, currently used as a first line vascular access in hemodialysis patients. The hypothesis is that the minimal dissection concept used in the RADAR inhibits venous juxta-anastomotic neointimal hyperplasia and stenosis, and lead to higher rates of maturation and patency.
Detailed Description
In current nephrology and vascular surgery guidelines, end-cephalic to side-radial arteriovenous fistula is the gold standard for primary vascular access creation. However, these wrist AVFs are recognized to have the worst patency of any autogenous vascular accesses. Outcome improvement is therefore urgent in the field of vascular access, which concerns a growing incident population of patients with end-stage renal disease requiring hemodialysis. Primary AVF failure, including failure to mature, occurs in ~35-40% in just the first year, generally due to juxta-anastomotic stenosis. Many AVF subsequently require additional interventions to mature successfully. The primary patency for these AVFs is poor with 55% at 12 months. Juxta-anastomotic neointimal hyperplasia typically occurs in the swing segment, e.g. the proximal vein mobilized to form the end-to-side anastomosis. This surgically-mobilized segment coincides both with turbulent flow as well as with devascularization of the vasa vasorum. These processes have been associated with endothelial cell activation and a dysfunctional phenotype. Therefore investigators hypothesized that surgical techniques which minimize venous dissection may improve fistula maturation and access patency. Accordingly, investigators developed the "Radial Artery Deviation And Reimplantation (RADAR) technique." Instead of using a traditional end-vein to side-artery anastomosis, RADAR uses an end-artery to side-vein anastomosis, additionally coupled with minimal vessel dissection. Investigators extend conventional "no touch" techniques and advocate avoidance of any venous dissection or manipulation. Investigators minimize arterial dissection as well, by dissecting the radial artery pedicle, not the artery itself. The aim of this study is to compare the safety and efficacy of this novel technique with the traditional radial-cephalic fistula in the setting of a multicenter randomized controlled trial. Besides traditional endpoints such as patency and reintervention rates, hand blood perfusion will be assessed with objective measurements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Renal Disease
Keywords
Vascular access, Hemodialysis, Arteriovenous fistula, Stenosis, Failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
arteriovenous fistula (AVF)
Arm Type
Active Comparator
Arm Description
Patient receiving a traditional arteriovenous fistula at the wrist (end-cephalic vein to side-radial artery)
Arm Title
RADAR
Arm Type
Experimental
Arm Description
Patient receiving an arteriovenous fistula at the wrist using the Radial Artery Deviation And Reimplantation technique (end-radial artery to side-cephalic vein)
Intervention Type
Procedure
Intervention Name(s)
End-cephalic vein to side-radial artery fistula creation
Intervention Description
Circumferential dissection of the cephalic vein (4-5cm long) Longitudinal arteriotomy (~10mm) End-vein to side-artery anastomosis using 7-0 polypropylene continuous suture
Intervention Type
Procedure
Intervention Name(s)
RADAR fistula creation
Intervention Description
Dissection of the anterior-medial aspect of the cephalic vein (~15mm) without grasping or clamping the venous wall Circumferential dissection of the radial artery pedicle (5cm long) and ligation of collaterals with surgical microclips Ligation and section of the radial artery (distal) Longitudinal venotomy (~10mm) End-artery to side-vein anastomosis using 7-0 polypropylene continuous suture
Primary Outcome Measure Information:
Title
Primary patency rate of the access
Time Frame
at 12 months
Secondary Outcome Measure Information:
Title
Assisted primary patency rate of the access
Time Frame
6 & 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient referred by the nephrologist for the creation of a primary vascular access Clinical examination of both upper limbs showing on the same limb: A cephalic vein at the distal third of the forearm Radial pulse Ulnar pulse Positive Allen test (patent palmar arches) Preoperative arterial and venous duplex ultrasound examination of both limbs showing on the same limb : A patent cephalic vein, ≥2mm in diameter at the distal 1/3 of the forearm, free from stenosis, ≥15cm in length A patent on dominant radial artery, ≥2mm in diameter at the distal 1/3 of the forearm, free from stenosis and major calcifications A patent ulnar artery, free from stenosis and major calcifications A positive Allen's test with assessment of the retrograde flow (patent palmar aches) Digital pressure >50mmHg when occlusive compression is made on the radial artery and digital/brachial ratio >0.5 Exclusion Criteria: patient under guardianship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nirvana SADAGHIANLOO, MD
Phone
+33492033835
Email
sadaghianloo.n@chu-nice.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Serge DECLEMY, MD
Organizational Affiliation
Vascular surgery, Nice University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Nice - Service de chirurgie vasculaire
City
Nice
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nirvana Sadaghianloo, MD
Phone
04 92 03 38 35
Email
sadaghianloo.n@chu-nice.fr
First Name & Middle Initial & Last Name & Degree
Serge DECLEMY
First Name & Middle Initial & Last Name & Degree
Nirvana SADAGHIANLOO

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluation of the Radial Artery Deviation And Reimplantation Technique for Primary Hemodialysis Access Creation

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