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Creating a Buttonhole Tunnel Track by Repeated Needling of the AV Fistula on the Same Day in Patients on Hemodialysis.

Primary Purpose

End-stage Renal Disease (ESRD)

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Repeated cannulation Buttonhole.
Single cannulation Buttonhole.
Sponsored by
Hospital of South West Jutland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-stage Renal Disease (ESRD) focused on measuring Buttonhole cannulation, Cannulation technique, Dialysis access, Hemodialysis, Arterio venous fistula

Eligibility Criteria

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

Inclusion Criteria:

  • chronic hemodialysis patients
  • at least 5 hemodialysis treatments with a blood flow ≥ 250 ml/min have been carried out
  • ability to speak and understand danish

Exclusion Criteria:

  • patients with an artificial heart valve
  • patients in high dose immunosuppressive treatment
  • patients with infections in their buttonholes
  • patients who are unable to provide informed consent

Sites / Locations

  • Hospital South West Jutland, EsbjergRecruiting
  • Kolding SygehusRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Repeated cannulation Buttonhole

Single cannulation Buttonhole

Arm Description

The intervention group (I): repeated needling into the same site in the AVF with sharp needles (4-6 pieces) at each dialysis (1-3 dialyses) creating a buttonhole tunnel track where cannulation with a blunt needle is possible.

The control group (C): needling into the same site in the AVF with 1 sharp needle at each dialysis (6-12 dialyses) creating a buttonhole tunnel track, where cannulation with a blunt needle is possible. .

Outcomes

Primary Outcome Measures

Buttonhole survival
Cannulation with a blunt needle in the buttonhole tunnel track is possible. Technique failure and non-survival is defined as inability to insert a blunt needle into the buttonhole tunnel tracks in three consecutive dialysis or inability to cannulate the established buttonhole track for more than two weeks.

Secondary Outcome Measures

Patient perceived pain post-needling
Measuring the patients pain at buttonhole needling using a validated numeric rating scale (NRS) for pain with 0 representing one pain extreme (e.g., "no pain") and 10 representing the other pain extreme (e.g., "pain as bad as you can imagine" and "worst pain imaginable"

Full Information

First Posted
June 6, 2019
Last Updated
May 7, 2021
Sponsor
Hospital of South West Jutland
Collaborators
Kolding Sygehus
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1. Study Identification

Unique Protocol Identification Number
NCT03989141
Brief Title
Creating a Buttonhole Tunnel Track by Repeated Needling of the AV Fistula on the Same Day in Patients on Hemodialysis.
Official Title
Creating a Buttonhole Tunnel Track by Repeated Needling of the AV Fistula on the Same Day in Patients on Hemodialysis.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 20, 2019 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital of South West Jutland
Collaborators
Kolding Sygehus

4. Oversight

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

5. Study Description

Brief Summary
BACKGROUND: The patients diagnosed with end stage renal disease require dialysis and for that they need to have a vascular access for hemodialysis (HD) placed. Vascular access complications are the most common cause of hospitalization among patients in HD. An AV fistula (AVF) is a surgical connection made between an artery and a vein, created by a vascular specialist, typically placed in an arm. AV fistulas are the preferred vascular access for long-term dialysis. In order to be able to carry out an adequate and uncomplicated dialysis treatment, two needles have to be placed in the fistula. It requires specialized technical ability to install well-functioning needles in the vessels of an AVF. The buttonhole technique is one of the two recommended techniques. For the buttonhole technique, two puncture sites are selected in the fistula. Here, exactly in the same spot a needle is inserted with the same angle and direction until a fibrous tunnel is formed, like a hole for an ear ring. Cannulation is now possible with blunt needles which are gentler and reduce complications. The time required to create a buttonhole tunnel is 6-12 cannulations, ie 6-12 dialyses. It is crucial for the future survival of the tunnel tracks, that a maximum of one to two persons cannulates until the track is created. This is a logistic challenge in a busy dialysis unit and may result in using a cannulation technique that is not recommended. A less time consuming method to create the buttonhole tunnel track may increase the use of the technique. A new method has been used in several dialysis units in Denmark. Using this method the tunnel tracks are created in 1-3 dialyses by repeated cannulations (4-6 needles one at a time) in the same two puncture sites in the fistula. The experiences so far indicates that this method reduces the dialysis sessions needed to create the tunnel tracks with 4-10 sessions. Thus, the logistic challenges of ensuring continuity in persons creating the tunnel track will be reduced. The purpose of the research project is to investigate whether a new method for creating buttonhole tunnels will: Increase the number of well-functioning buttonholes. Be less painful for the patient. Reduce the number of dialysis needed to create the buttonhole tunnel track. Cause unchanged or fewer fistula associated complications and infections.
Detailed Description
Background: See above. Aims:To study whether a new method of creating a buttonhole tunnel tracks can reduce the incidence of buttonhole technique failure and the patients pain with needling. Patients and Methods: A randomized, multi-center study enrolling 42 patients in hemodialysis from two HD units in Denmark. The study will begin end of May 2019. Participants are randomized into 2 groups where cannulation will be carried out by a small group of dialysis nurses with experience and skills in buttonhole cannulation. In both groups the same nurse will carry out the cannulation the first four dialysis sessions. At the following sessions the cannulation will be carried out by the nurse/nurses responsible for the patient. The procedures throughout the study will be the same in both participating centers. The control group (K): creating buttonhole tunnels according to the standard method, ie. cannulation with a single sharp cannula in the AVF at each dialysis for 6-12 dialyses until a blunt needle can be inserted. The intervention group (I): creating buttonhole tunnels according to the new method, ie. repeated cannulation with several sharp needles (4-6 pieces) at each dialysis for 1-3 dialyses until a blunt cannula can be inserted. The creation of a buttonhole tunnel track is defined as completed when two consecutive dialyses have been carried out with no use of sharp needles, however no longer than 24 dialysis sessions.Thus, the period of time will be of different length for each participant. In the period until the tunnel is created, data will be collected at each dialyses regarding number of cannulations, type of needle (sharp or blunt), cannulator and patient-experienced pain with needling. The primary outcome is buttonhole technique failure defined as the need for cannulations carried out using sharp needles in the buttonhole for three consecutive dialyses or in case lack of ability to insert blunt needles in the buttonhole for 2 weeks. Follow-up from the date of the completed creation of the buttonhole tunnel track in both groups: 12 month ongoing follow-up of the primary outcome buttonhole survival and the secondary outcomes AVF associated infections, complications and AVF survival. Sample size:The power calculation is based on the expected incidence of the primary outcome measure: buttonhole technique failure. Based on calculations in the two dialysis centers from randomly selected patients with buttonhole tunnels made using the intervention and the control method, it appears that the estimated buttonhole technique failure is 10 % and 30 %, respectively. Drop-off rate is estimated to 30%. The number of participants for the study is calculated at 21 subjects in each group to achieve a power of 0.8 with a type error rate of 0.5. Intention-to-treat analysis will be carried out. Censoring in case of death, if the person wants to withdraw from the study or moves, AV fistula failure for non-buttonhole associated causes and kidney transplant. Statistical analysis:The baseline characteristics of the study population will be presented as counts and proportions and compared between randomization groups with chi-square test / Fisher's exact test (depending on number of observations) for categorical variables. Continous variables will be presented as mean (SD), respectively, median (IQR) depending on normality of data and compared between groups by t-test, respectively, Wilcoxon rank-sum test. Normality will be evaluated by quantile plots and Shapiro-Wilks test. Moreover, repeated measurements will be compared by mixed effects models. Time to event outcomes will be compared by the Kaplan-Meier method and tested by log-rank test, furthermore discrete time survival methods will be applied as a sensitivity analysis. P-values <0.05 are regarded as statistically significant. Follow-up will be censored at 1 year. Statistical analysis will be performed using Stata, version 11.0 (StataCorp, College Station, Tex., USA).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Renal Disease (ESRD)
Keywords
Buttonhole cannulation, Cannulation technique, Dialysis access, Hemodialysis, Arterio venous fistula

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
42 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Repeated cannulation Buttonhole
Arm Type
Experimental
Arm Description
The intervention group (I): repeated needling into the same site in the AVF with sharp needles (4-6 pieces) at each dialysis (1-3 dialyses) creating a buttonhole tunnel track where cannulation with a blunt needle is possible.
Arm Title
Single cannulation Buttonhole
Arm Type
Active Comparator
Arm Description
The control group (C): needling into the same site in the AVF with 1 sharp needle at each dialysis (6-12 dialyses) creating a buttonhole tunnel track, where cannulation with a blunt needle is possible. .
Intervention Type
Procedure
Intervention Name(s)
Repeated cannulation Buttonhole.
Other Intervention Name(s)
Intervention method
Intervention Description
The intervention group (I): repeated needling into the same site in the AVF with sharp needles (4-6 pieces) at each dialysis (1-3 dialyses) creating a buttonhole tunnel track where cannulation with a blunt needle is possible.
Intervention Type
Procedure
Intervention Name(s)
Single cannulation Buttonhole.
Other Intervention Name(s)
Standard method
Intervention Description
The control group (C): needling into the same site in the AVF with 1 sharp needle at each dialysis (6-12 dialyses) creating a buttonhole tunnel track, where cannulation with a blunt needle is possible. .
Primary Outcome Measure Information:
Title
Buttonhole survival
Description
Cannulation with a blunt needle in the buttonhole tunnel track is possible. Technique failure and non-survival is defined as inability to insert a blunt needle into the buttonhole tunnel tracks in three consecutive dialysis or inability to cannulate the established buttonhole track for more than two weeks.
Time Frame
Follow up for 1 year after completed creation of buttonhole tunnel
Secondary Outcome Measure Information:
Title
Patient perceived pain post-needling
Description
Measuring the patients pain at buttonhole needling using a validated numeric rating scale (NRS) for pain with 0 representing one pain extreme (e.g., "no pain") and 10 representing the other pain extreme (e.g., "pain as bad as you can imagine" and "worst pain imaginable"
Time Frame
Measured at each cannulation until completed creation of buttonhole tunnel track (up to 24 dialyses=8 weeks)
Other Pre-specified Outcome Measures:
Title
Number of dialyses required to create a buttonhole tunnel track
Description
A buttonhole tunnel track is considered created when 2 consecutive dialyses have been carried out using blunt needles with no use of sharp needles. Failure in creation: when the tunnel can't be needled with a blunt needle after 24 dialyses
Time Frame
up to 24 dialyses=8 weeks
Title
AV fistula associated event
Description
buttonhole infections, AV fistula infections, AV fistula failure, surgical fistula interventions (thrombosis, aneurysm, stenosis, steal syndrome).
Time Frame
Follow up for 1 year after completed creation of buttonhole tunnel

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: chronic hemodialysis patients at least 5 hemodialysis treatments with a blood flow ≥ 250 ml/min have been carried out ability to speak and understand danish Exclusion Criteria: patients with an artificial heart valve patients in high dose immunosuppressive treatment patients with infections in their buttonholes patients who are unable to provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mette KM Axelsen, RN, MHS
Phone
+045 79182260
Email
Mette.Kirstine.Molgaard.Axelsen@rsyd.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Bibi Gram
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mette KM Axelsen, RN,MHS
Organizational Affiliation
Hospital SWJ
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital South West Jutland, Esbjerg
City
Esbjerg
ZIP/Postal Code
6700
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mette KM Axelsen, RN,MHS
Phone
+045 79182260
Email
Mette.Kirstine.Molgaard.Axelsen@rsyd.dk
Facility Name
Kolding Sygehus
City
Kolding
ZIP/Postal Code
6000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nanna Lagoni, RN
Phone
+045 7636 0450
Email
Nanna.Lagoni@rsyd.dk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Creating a Buttonhole Tunnel Track by Repeated Needling of the AV Fistula on the Same Day in Patients on Hemodialysis.

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