Hemocontrol and Blood Pressure Control in Dialysis Patients
Primary Purpose
End-Stage Renal Disease, Hemodialysis
Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Hemocontrol Biofeedback System
Sponsored by
About this trial
This is an interventional treatment trial for End-Stage Renal Disease focused on measuring End-stage renal disease, Hemodialysis, Hypertension, Hypotension, Blood volume, Hypervolemia, Quality of life, Biofeedback system
Eligibility Criteria
Inclusion Criteria: 18 years or older chronic hemodialysis on renal replacement therapy > 3 months at least 3 dialysis sessions and 9 hours of therapy weekly willing to measure blood pressure at home able to sign an informed consent Exclusion Criteria: anticipated change in renal replacement therapy anticipated transfer to another center planned renal transplantation enrollment in another clinical trial
Sites / Locations
- Hopital du Sacre-Coeur de Montreal
Outcomes
Primary Outcome Measures
Difference from baseline to end of study in ambulatory blood pressure control
Secondary Outcome Measures
Episodes of intra-dialytic hypotension requiring nursing interventions
Health-related quality of life (using the Kidney Disease and Quality of Life Short Form)
Full Information
NCT ID
NCT00319774
First Posted
April 27, 2006
Last Updated
April 27, 2006
Sponsor
Université de Montréal
Collaborators
Gambro Renal Products, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00319774
Brief Title
Hemocontrol and Blood Pressure Control in Dialysis Patients
Official Title
Assessment of Hemocontrol Biofeedback System Efficiency on Long Term Blood Pressure Control, Nursing Interventions, and Quality of Life in Hemodialysis Patients: a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2003
Overall Recruitment Status
Completed
Study Start Date
December 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2003 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Université de Montréal
Collaborators
Gambro Renal Products, Inc.
4. Oversight
5. Study Description
Brief Summary
Volume overload contributes significantly to the pathogenesis of hypertension in hemodialysis patients. The Hemocontrol(HC)system (Gambro), which automatically adjusts ultrafiltration rate and dialysate conductivity according to blood volume variations during dialysis, has been suggested to improve hemodynamic tolerance and thus facilitate fluid removal.
This randomized controlled trial was designed to compare the use of HC with standard hemodialysis to test the hypothesis that the use of the HC system may lower home blood pressure in comparison with standard hemodialysis as a primary endpoint. Secondary endpoints are a variation in the percentage of dialysis sessions requiring nurses' interventions for intra-dialytic hypotension and a change in the health-related quality of life of HD patients.
Detailed Description
Hypertension is a common problem in patients undergoing chronic maintenance hemodialysis (HD) with a reported prevalence of 50 to 90 % [Hörl, 2002]. As a major risk factor for cardiovascular disease, hypertension contributes to the high rate of morbidity and mortality in ESRD patients [Foley, 1996; Port, 1999]. For a majority of dialysis patients, volume overload (VO) plays a major role in the pathogenesis of hypertension [Fishbane, 1996; Rahman, 2000; Ventura, 1997] and removing excess volume can often normalize blood pressure [Fishbane, 1996]. Unfortunately, correcting VO frequently proves to be difficult because of hemodynamic instability during HD sessions. As much as 20 to 50% of dialysis patients present with symptoms of intradialytic hypotension (IDH) [Santoro, 2002]. IDH increases nursing work load and negatively affects the efficacy of dialysis and the quality of life of HD patients. Different measures are used to avoid IDH, such as limitation of salt and water intake, avoidance of antihypertensive medication before dialysis, utilization of low temperature dialysate, and modeling of ultrafiltration and/or dialysate conductivity. These measures often generate mixed results.
The Hemocontrol (HC) biofeedback system (Gambro®) has been reported to reduce hemodynamic instability and hypotensive episodes during hemodialysis [Basile, 2001; Begin, 2002; Ronco, 2000; Santoro, 1994; Santoro, 1998; Santoro, 2002; Wolkotte, 2002]. The HC system consists in a fully integrated biofeedback system that monitors and regulates blood volume contraction during hemodialysis through software-driven adjustments of ultrafiltration rate and dialysate conductivity. By improving hemodynamic tolerance during dialysis, the use of the HC system has been suggested to facilitate fluid removal and correction of VO, leading to improved control of hypertension.
The present randomized controlled trial was designed to test the hypothesis that the use of the HC system would lower home BP in comparison with standard hemodialysis as a primary endpoint. Secondary endpoints are a variation in the percentage of HD sessions requiring nurses' interventions and a change in the health-related quality of life of HD patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-Stage Renal Disease, Hemodialysis
Keywords
End-stage renal disease, Hemodialysis, Hypertension, Hypotension, Blood volume, Hypervolemia, Quality of life, Biofeedback system
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (false)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Hemocontrol Biofeedback System
Primary Outcome Measure Information:
Title
Difference from baseline to end of study in ambulatory blood pressure control
Secondary Outcome Measure Information:
Title
Episodes of intra-dialytic hypotension requiring nursing interventions
Title
Health-related quality of life (using the Kidney Disease and Quality of Life Short Form)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years or older
chronic hemodialysis
on renal replacement therapy > 3 months
at least 3 dialysis sessions and 9 hours of therapy weekly
willing to measure blood pressure at home
able to sign an informed consent
Exclusion Criteria:
anticipated change in renal replacement therapy
anticipated transfer to another center
planned renal transplantation
enrollment in another clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francois Madore, MD
Organizational Affiliation
Faculty of Medicine, University of Montreal
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hopital du Sacre-Coeur de Montreal
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4J 1C5
Country
Canada
12. IPD Sharing Statement
Citations:
Citation
C. Déziel, M. Zellweger, R. Comeau, A. Valleau, S. Raymond-Carrier, F. Madore. Home Blood Pressure Management with Automated Blood Volume Regulation in Hemodialysis Patients: A Prospective Randomized Controlled Trial. J. Am. Soc. Nephrol. 15:594A, October 2004.
Results Reference
background
Citation
C. Déziel, M. Zellweger, R. Comeau, M. Kerangueven, S. Raymond-Carrier, F. Madore. Hemodynamic Stability during Hemodialysis and Quality of Life with Automated Blood Volume Regulation: A Prospective Randomized Controlled Trial. J. Am. Soc. Nephrol. 15:47A, October 2004
Results Reference
background
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Hemocontrol and Blood Pressure Control in Dialysis Patients
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