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Benefit of Ultrasound Guidance in Arteriovenous Fistula (AVF) Cannulation in Pediatric Hemodialysis (PafusGuC)

Primary Purpose

Arteriovenous Fistula Cannulation

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Ultrasound-guided AVF cannulation method
Conventional AVF cannulation method
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Arteriovenous Fistula Cannulation focused on measuring Arteriovenous fistula AVF, Pediatric hemodialysis, Cannulation

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pediatric patients ˂ 18 years of age at enrollment
  • Patients with end-stage renal disease undergoing hemodialysis therapy
  • Patients carrying an arteriovenous fistula created more than 6 weeks before enrollment
  • Prior agreement of the patient and their legal representative by signing the parent's informed consent form
  • Patients affiliated to social security system

Exclusion Criteria:

  • Non-matured arteriovenous fistula according to the referring pediatrician
  • Patients undergoing dialysis at least partly through a central venous catheter
  • Estimated duration of dialysis less than 1 month in the investigation center
  • Participation in other intervention research

Sites / Locations

  • Uh MontpellierRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Ultrasound-guided AVF cannulation method

Conventional AVF cannulation method

Arm Description

The AVF cannulation is carried out using ultrasoud guidance

The AVF cannulation is carried out by palpation

Outcomes

Primary Outcome Measures

Compare the rate of inadequate dialysis after ultrasound-guided AVF cannulation vs. conventional cannulation in pediatric patients (<18 years) with end-stage renal disease undergoing hemodialysis therapy.
Inadequate dialysis is defined by the presence of one of the following parameters: Blood flow rate (BFR expressed in ml/min corresponding to the volume of blood in milliliters that flows per minute) less than 80% of adequate blood flow corresponding to a flow ≥ 7 ml per kilograms of weight with a maximum of 300 ml/min Requirement of single-needle dialysis after 3 cannulation failures Early discontinuation of hemodialysis Loss of dialysis circuit during the session Out of range arterial or venous pressure during dialysis requiring a drop in blood flow rate Purification coefficient defined by Kt/V <1.2: K represents the dialyzer clearance of urea (expressed in milliliters/ min and corresponds to the volume of blood in ml cleared of urea per minute ) // t (in minutes) represents the dialysis time duration // V (in milliliters) represents the volume of distribution of urea, and equals the patient's total body water

Secondary Outcome Measures

Number of cannulations required for the insertion of the 2 dialysis catheters
Compare the number of cannulations required for the insertion of the 2 dialysis catheters in conventional method vs ultrasound-guided method
The time required for the insertion of the 2 catheters
Compare the time required for the insertion of the 2 catheters in conventional method vs ultrasound-guided method
The occurrence of cannulation complications
Compare the occurrence of cannulation complications (hematoma, diffusion, aneurysm, etc.) in conventional method vs ultrasound-guided method
The occurrence of dialysis incidents caused by catheters dysfunction
Compare the occurrence of dialysis incidents caused by catheters dysfunction (decrease in dialysis flow, single-puncture dialysis, shortening of dialysis time, loss of circuit) in conventional method vs ultrasound-guided method
Patient satisfaction
Compare the patient satisfaction in conventional method vs ultrasound-guided method using a satisfaction questionnaire
Patient comfort
Compare the patient comfort in conventional method vs ultrasound-guided method. The visual analogue scale (VAS) will be used by patients > 5 years of age. The VAS measures from 0 to 10 the intensity of pain. The higher the score the less comfortable the procedure
Patient comfort
Compare the patient comfort in conventional method vs ultrasound-guided method. The neonatal pain and discomfort scale (EDIN Échelle Douleur Inconfort Nouveau-Né ) will be used by patients ≤ 5 years of age. The EDIN scale uses five behavioural indicators of pain: facial activity, body movements, quality of sleep, quality of contact with nurses, and consolability. The scale measures friom 0 to 15 the intensity of pain. The higher the score the less comfortable the procedure

Full Information

First Posted
September 13, 2022
Last Updated
December 21, 2022
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT05556915
Brief Title
Benefit of Ultrasound Guidance in Arteriovenous Fistula (AVF) Cannulation in Pediatric Hemodialysis
Acronym
PafusGuC
Official Title
Intérêt de l'échoguidage Dans Les Ponctions de Fistule artério-veineuse en hémodialyse pédiatrique
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 3, 2022 (Actual)
Primary Completion Date
June 3, 2025 (Anticipated)
Study Completion Date
June 3, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

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 arteriovenous fistula (AVF) is the reference hemodialysis vascular access for both adult and pediatric patients. The cannulation quality is decisive for the quality of the dialysis. Difficult AVF cannulations are more frequent in pediatrics than in adults. Recent studies in adults have shown that ultrasound-guided AVF cannulation improves the cannulation quality and therefore the quality of dialysis. This study aims to prove that ultrasound-guided AVF cannulation in children will improve the quality of dialysis overall.
Detailed Description
The European and American recommandations emphasize that the arteriovenous fistula (AVF) is the first choice vascular access in hemodialysis for both adult and pediatric patients. Indeed, infections and thrombotic complications are lower with an AVF than with a central venous catheter. In addition, the efficiency of dialysis is better in patients with AVF in both pediatric and adult patients. The pediatric population has its own characteristics. On the one hand, the size of the vessels, in particular in patients weighing less than 20 kilos, complicates the creation of the AVF. On the other hand, the time for AVF maturation in children (corresponding to the time required between the creation of the AVF and its use) is much higher than that of the adult population. These specific anatomical characteristics partly explain the more frequent AVF cannulation difficulties in pediatric patients. Inadequate dialysis is considered to be a session in which the therapy goals were not achieved. This rate of inadequate dialysis is estimated at 8-10% in children due to vascular access problem, whereas this rate is only 1 to 5% in adults. There is also an increase in side effects related to these pediatric AVF cannulation difficulties (trauma, hematoma, edema following diffusion, etc.) responsible for inadequate dialysis and, in the long term, AVF dysfunction (stenosis, thrombosis). The preservation of the vascular access by means of new cannulation techniques aimed at limiting trauma is therefore a primary objective in pediatric hemodialysis. The introduction of new cannulation methods as well as the training of nurses/childcare workers in the various puncture techniques would thus make it possible to improve the quality of dialysis sessions, the lifespan of AVFs, to increase the number of puncture sites and reduce the number of punctures per session and the occurrence of complications. Recently, the ultrasound-guided AVF cannulation technique has shown promising results in adults with regard to the prevention of vascular access complications, the feeling of pain and the obtaining of adequate dialysis. A recent review points to the need to confirm the benefit of ultrasound-guided cannulation through randomized studies, the current data being promising but needing to be confirmed. To date, no data concerning the benefit of ultrasound-guided cannulation in pediatrics is available in the literature. Our project will therefore be the first research to compare 2 AVF cannulation methods in pediatric hemodialysis. The hypothesis adopted is that the AVF cannulation using ultrasound guidance in children undergoing dialysis will allow an overall improvement of dialysis quality, a reduction of complication occurrence and an improvement of patient comfort.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arteriovenous Fistula Cannulation
Keywords
Arteriovenous fistula AVF, Pediatric hemodialysis, Cannulation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Open label, randomized clinical study comparing two AVF cannulation methodes (conventional vs ultrasound-guided method) in pediatric patients with end-stage renal disease undergoing hemodialysis therapy.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ultrasound-guided AVF cannulation method
Arm Type
Experimental
Arm Description
The AVF cannulation is carried out using ultrasoud guidance
Arm Title
Conventional AVF cannulation method
Arm Type
Other
Arm Description
The AVF cannulation is carried out by palpation
Intervention Type
Other
Intervention Name(s)
Ultrasound-guided AVF cannulation method
Intervention Description
For ultrasound-guided cannulation, the same ultrasound device will be used for all patients (TE5-POC ultrasound MINDRAY® system). The ultrasound device will identify the AVF aspect , the location including the depth (distance from the skin surface) , the vessel diameter and guide the cannulation in real-time. The device will be disinfected between uses and covered with a transparent adhesive film to avoid any direct contact with the patient. Sterile gel will be used for the cannulation.
Intervention Type
Other
Intervention Name(s)
Conventional AVF cannulation method
Intervention Description
The AVF cannulation is carried out by palpation. This technique consists of manually evaluating the position, direction and depth of the fistula in order to determine the puncture site where the 2-dialysis catheters will be inserted. After local asepsis, the AVF is therefore needled at 2 points 5 cm apart.
Primary Outcome Measure Information:
Title
Compare the rate of inadequate dialysis after ultrasound-guided AVF cannulation vs. conventional cannulation in pediatric patients (<18 years) with end-stage renal disease undergoing hemodialysis therapy.
Description
Inadequate dialysis is defined by the presence of one of the following parameters: Blood flow rate (BFR expressed in ml/min corresponding to the volume of blood in milliliters that flows per minute) less than 80% of adequate blood flow corresponding to a flow ≥ 7 ml per kilograms of weight with a maximum of 300 ml/min Requirement of single-needle dialysis after 3 cannulation failures Early discontinuation of hemodialysis Loss of dialysis circuit during the session Out of range arterial or venous pressure during dialysis requiring a drop in blood flow rate Purification coefficient defined by Kt/V <1.2: K represents the dialyzer clearance of urea (expressed in milliliters/ min and corresponds to the volume of blood in ml cleared of urea per minute ) // t (in minutes) represents the dialysis time duration // V (in milliliters) represents the volume of distribution of urea, and equals the patient's total body water
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of cannulations required for the insertion of the 2 dialysis catheters
Description
Compare the number of cannulations required for the insertion of the 2 dialysis catheters in conventional method vs ultrasound-guided method
Time Frame
During procedure
Title
The time required for the insertion of the 2 catheters
Description
Compare the time required for the insertion of the 2 catheters in conventional method vs ultrasound-guided method
Time Frame
During procedure
Title
The occurrence of cannulation complications
Description
Compare the occurrence of cannulation complications (hematoma, diffusion, aneurysm, etc.) in conventional method vs ultrasound-guided method
Time Frame
During procedure
Title
The occurrence of dialysis incidents caused by catheters dysfunction
Description
Compare the occurrence of dialysis incidents caused by catheters dysfunction (decrease in dialysis flow, single-puncture dialysis, shortening of dialysis time, loss of circuit) in conventional method vs ultrasound-guided method
Time Frame
During procedure
Title
Patient satisfaction
Description
Compare the patient satisfaction in conventional method vs ultrasound-guided method using a satisfaction questionnaire
Time Frame
30 days, 90 days, 180 days and 12 months after enrollment
Title
Patient comfort
Description
Compare the patient comfort in conventional method vs ultrasound-guided method. The visual analogue scale (VAS) will be used by patients > 5 years of age. The VAS measures from 0 to 10 the intensity of pain. The higher the score the less comfortable the procedure
Time Frame
During the procedure
Title
Patient comfort
Description
Compare the patient comfort in conventional method vs ultrasound-guided method. The neonatal pain and discomfort scale (EDIN Échelle Douleur Inconfort Nouveau-Né ) will be used by patients ≤ 5 years of age. The EDIN scale uses five behavioural indicators of pain: facial activity, body movements, quality of sleep, quality of contact with nurses, and consolability. The scale measures friom 0 to 15 the intensity of pain. The higher the score the less comfortable the procedure
Time Frame
During the procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pediatric patients ˂ 18 years of age at enrollment Patients with end-stage renal disease undergoing hemodialysis therapy Patients carrying an arteriovenous fistula created more than 6 weeks before enrollment Prior agreement of the patient and their legal representative by signing the parent's informed consent form Patients affiliated to social security system Exclusion Criteria: Non-matured arteriovenous fistula according to the referring pediatrician Patients undergoing dialysis at least partly through a central venous catheter Estimated duration of dialysis less than 1 month in the investigation center Participation in other intervention research
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean Philippe BOUDET
Phone
04 67 33 66 38
Email
jp-boudet@chu-montpellier.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Philippe BOUDET
Organizational Affiliation
University Hospital, Montpellier
Official's Role
Principal Investigator
Facility Information:
Facility Name
Uh Montpellier
City
Montpellier
ZIP/Postal Code
34295
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
FILA, MD
Ext
33
Email
fila@chu-montpellier.fr

12. IPD Sharing Statement

Plan to Share IPD
No

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Benefit of Ultrasound Guidance in Arteriovenous Fistula (AVF) Cannulation in Pediatric Hemodialysis

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