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Implantable Loop Recorder in Hemodialysis Patients (RYTHMODIAL)

Primary Purpose

Hemodialysis, Cardiac Arrhythmia, Cardiac Death

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Implantation of ILR
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hemodialysis focused on measuring Hemodialysis, Cardiac Arrhythmia, Cardiac Death, Implantable Loop Recorder

Eligibility Criteria

45 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients under chronic hemodialysis
  • Age between 45 and 80 yo
  • written informed consent
  • affiliated to the French Social Security system

Exclusion Criteria:

  • Pace-maker or Implantable Cardioverter Defibrillator
  • Active infection
  • Neoplasia or any pathology with a life expectancy <12 months
  • Cachexia
  • Patient with restricted civic rights by law

Sites / Locations

  • Clinique Saint Augustin
  • University Hospital of Bordeaux
  • Polyclinique Bordeaux-Nord Aquitaine
  • CH de Haguenau
  • CH de Libourne
  • CHU de Nantes
  • CHU de Rennes
  • CHU de Strasbourg
  • CHU de Toulouse

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Implantable loop recorder (ILR) in hemodialysis patients

Arm Description

implantation of loop recorder in hemodialysis patients

Outcomes

Primary Outcome Measures

Occurrence of arrhythmia
Type 1: Conduction disorders: 1A-Cardiac arrest, 1B-High degree AV Block, 1C-Sinus dysfunction (Sinus pause>3seconds, Bradycardia <30 bpm) Type 2: Ventricular rhythm disorders ≥ 150 bpm: 2A-Polymorphic ventricular tachycardia, Torsades de pointe, Ventricular Fibrillation, 2B-Sustained ventricular tachycardia (>30 seconds), 2C- Non sustained ventricular tachycardia (>4 beats but <30 seconds)

Secondary Outcome Measures

Study correlation between arrhythmic events (primary outcome) and hemodialysis parameters (general: day of dialysis, length of dialysis;clinical: weight variation during dialysis...; biological: potassium level, potassium variation...; ECG)
Incidence of supra-ventricular arrhythmia: 3A-Atrial Fibrillation, 3B-Atrial Tachycardia, 3C-Junctional tachycardia

Full Information

First Posted
November 4, 2010
Last Updated
November 23, 2017
Sponsor
University Hospital, Bordeaux
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1. Study Identification

Unique Protocol Identification Number
NCT01252823
Brief Title
Implantable Loop Recorder in Hemodialysis Patients
Acronym
RYTHMODIAL
Official Title
Identification and Prevention of Sudden Cardiac Death Causes in Hemodialysis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
December 28, 2010 (Actual)
Primary Completion Date
February 29, 2016 (Actual)
Study Completion Date
February 29, 2016 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to use implantable loop recorder (ILR) in patients under chronic hemodialysis to record arrhythmias and conduction disorders and correlate them with hemodialysis parameters.
Detailed Description
Primary cause of death in patients under chronic hemodialysis is Sudden Cardiac Death (SCD) (25% of all cause mortality). SCD is mainly due to cardiac arrhythmias (conduction disturbances or ventricular arrhythmias). These cardiac arrhythmias are highly sensitive to hydro-electrolytic disorders which are extremely frequent in patients under hemodialysis. In addition, other conditions leading to cardiac arrhythmias are frequent in this population such as ischemic myocardiopathy or dilated myocardiopathy. However, so far, little is known about the occurrence of arrhythmias because of studies using only standard Holter monitoring (24 to 48 hours monitoring at best). The investigators sought to evaluate the incidence of cardiac arrhythmias by using an implantable loop recorder (ILR)(Reveal XT, Medtronic) that allows continuous rhythm monitoring for 24 months. This ILR will be implanted under local anesthesia. Clinical follow-up will be performed during hemodialysis and rhythm management will be performed automatically using a remote-monitoring system (Carelink, Medtronic). Pre-programmed alerts (conduction disturbances, supra-ventricular arrhythmias or ventricular arrhythmias) recorded by the ILR will be sent automatically on a daily basis in our center. These data will be analyzed during week days from 9AM to 5PM. They will be reviewed by an electrophysiologists and depending on the potential lethality, the patients will be called and ask to come to the emergency room in case of high risk or the nephrologist will be contacted and he will see the patients during the next hemodialysis in case of on vital event.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodialysis, Cardiac Arrhythmia, Cardiac Death
Keywords
Hemodialysis, Cardiac Arrhythmia, Cardiac Death, Implantable Loop Recorder

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Implantable loop recorder (ILR) in hemodialysis patients
Arm Type
Experimental
Arm Description
implantation of loop recorder in hemodialysis patients
Intervention Type
Device
Intervention Name(s)
Implantation of ILR
Intervention Description
Subcutaneous implantation of ILR under local anesthesia
Primary Outcome Measure Information:
Title
Occurrence of arrhythmia
Description
Type 1: Conduction disorders: 1A-Cardiac arrest, 1B-High degree AV Block, 1C-Sinus dysfunction (Sinus pause>3seconds, Bradycardia <30 bpm) Type 2: Ventricular rhythm disorders ≥ 150 bpm: 2A-Polymorphic ventricular tachycardia, Torsades de pointe, Ventricular Fibrillation, 2B-Sustained ventricular tachycardia (>30 seconds), 2C- Non sustained ventricular tachycardia (>4 beats but <30 seconds)
Time Frame
Checked every days except Sundays and bank holidays during 24 Month
Secondary Outcome Measure Information:
Title
Study correlation between arrhythmic events (primary outcome) and hemodialysis parameters (general: day of dialysis, length of dialysis;clinical: weight variation during dialysis...; biological: potassium level, potassium variation...; ECG)
Time Frame
three times per weeks, at each hemodialysis
Title
Incidence of supra-ventricular arrhythmia: 3A-Atrial Fibrillation, 3B-Atrial Tachycardia, 3C-Junctional tachycardia
Time Frame
Checked every days except Sundays and bank holidays during 24 Month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients under chronic hemodialysis Age between 45 and 80 yo written informed consent affiliated to the French Social Security system Exclusion Criteria: Pace-maker or Implantable Cardioverter Defibrillator Active infection Neoplasia or any pathology with a life expectancy <12 months Cachexia Patient with restricted civic rights by law
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian COMBE, MD-PhD
Organizational Affiliation
University Hospital of Bordeaux, France
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Antoine BENARD, MD
Organizational Affiliation
USMR, University Hospital of Bordeaux, France
Official's Role
Study Chair
Facility Information:
Facility Name
Clinique Saint Augustin
City
Bordeaux
ZIP/Postal Code
33074
Country
France
Facility Name
University Hospital of Bordeaux
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Facility Name
Polyclinique Bordeaux-Nord Aquitaine
City
Bordeaux
ZIP/Postal Code
33077
Country
France
Facility Name
CH de Haguenau
City
Haguenau
Country
France
Facility Name
CH de Libourne
City
Libourne
Country
France
Facility Name
CHU de Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
CHU de Rennes
City
Rennes
ZIP/Postal Code
35033
Country
France
Facility Name
CHU de Strasbourg
City
Strasbourg
ZIP/Postal Code
67091
Country
France
Facility Name
CHU de Toulouse
City
Toulouse
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
30089568
Citation
Sacher F, Jesel L, Borni-Duval C, De Precigout V, Lavainne F, Bourdenx JP, Haddj-Elmrabet A, Seigneuric B, Keller A, Ott J, Savel H, Delmas Y, Bazin-Kara D, Klotz N, Ploux S, Buffler S, Ritter P, Rondeau V, Bordachar P, Martin C, Deplagne A, Reuter S, Haissaguerre M, Gourraud JB, Vigneau C, Mabo P, Maury P, Hannedouche T, Benard A, Combe C. Cardiac Rhythm Disturbances in Hemodialysis Patients: Early Detection Using an Implantable Loop Recorder and Correlation With Biological and Dialysis Parameters. JACC Clin Electrophysiol. 2018 Mar;4(3):397-408. doi: 10.1016/j.jacep.2017.08.002. Epub 2017 Sep 27.
Results Reference
derived

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Implantable Loop Recorder in Hemodialysis Patients

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