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Effect of Increased Convective Clearance by On-Line Hemodiafiltration on All Cause Mortality in Chronic Hemodialysis Patients (CONTRAST)

Primary Purpose

End-stage Renal Disease, Cardiovascular Disease

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
on-line hemodiafiltration
low flux hemodialysis
Sponsored by
Amsterdam UMC, location VUmc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-stage Renal Disease focused on measuring online hemodiafiltration, low flux hemodialysis, cardiovascular disease, endothelial dysfunction, uremic toxicity, quality of life, nutritional status

Eligibility Criteria

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

Inclusion Criteria: Patients treated by HD 2 or 3 times a week, for at least 2 months Patients able to understand the study procedures Patients willing to provide written informed consent Exclusion Criteria: Current age < 18 years Treatment by HDF or high flux HD in the preceding 6 months Severe incompliance (severe non-adherence to the dialysis procedure and accompanying prescriptions, especially frequency and duration of dialysis treatment and fluid restriction) Life expectancy < 3 months due to non renal disease Participation in other clinical intervention trials evaluating cardiovascular outcome

Sites / Locations

  • Dr Georges-L. Dumont Regional Hospital
  • Centre Hospitalier de L'Université de Montreal, Hopital Notre Dame
  • Jeroen Bosch Ziekenhuis
  • Medisch Centrum Alkmaar
  • Vrije Universiteit Medisch Centrum
  • Onze Lieve Vrouwe Gasthuis
  • Academical Medical Center
  • Ziekenhuis Rijnstate
  • Dialyse Kliniek Noord
  • Haga Ziekenhuis (locatie Leyenburg)
  • Slingeland Ziekenhuis
  • Ziekenhuis Gelderse Vallei
  • Catharina Ziekenhuis
  • Oosterscheldeziekenhuis
  • Groene Hart Ziekenhuis
  • Martini Ziekenhuis
  • Rijnland Ziekenhuis
  • University Medical Center St Radboud
  • Franciscus Ziekenhuis
  • Sint Franciscus Gasthuis
  • Medisch Centrum Rijnmond Zuid - locatie Clara
  • Orbis Medisch en Zorgcentrum
  • Ziekenhuis Zeeuws-Vlaanderen
  • St Elisabeth Ziekenhuis
  • Stichting Dianet
  • University Medical Center Utrecht
  • VieCuri Medisch Centrum
  • Isala Klinieken
  • Haukeland Universitetssykehus

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Active Comparator

Arm Label

1: low flux hemodialysis

2 on-line hemodiafiltration

Arm Description

standard treatment

Outcomes

Primary Outcome Measures

all cause mortality

Secondary Outcome Measures

fatal and non-fatal cardiovascular events
Left ventricular mass index (LVMi), carotid IMT (intima media thickness), aortic pulse wave velocity (PWV)
laboratory markers of endothelial dysfunction, micro-inflammation, oxidative stress
lipid profiles, uremic toxins
quality of life
nutritional state
anemia management
hemoglobin levels, erythropoietin use / resistance iron saturation / ferritin levels, prescription of iron medication
cost utility analysis
hospital admissions
hospitalization days hospital admission for infections hospital admission for any cause
blood pressure and antihypertensive medication
residual kidney function
mineral bone disease
laboratory parameters of mineral bone disease and medication (phosphate binders, vitamin D (or analogues), cinacalet)
parameters of treatment / treatment delivery
dialysis efficiency (Kt/V urea); bloodflow, dialysate flow, ultrafiltration volume, (HDF:) convection volume

Full Information

First Posted
September 12, 2005
Last Updated
January 20, 2011
Sponsor
Amsterdam UMC, location VUmc
Collaborators
UMC Utrecht, Medical Center Alkmaar, Maasstad Hospital, Julius Center for Health Sciences and Primary Care, Utrecht, Dutch Kidney Foundation, Fresenius Medical Care North America, Gambro Renal Products, Inc., Baxter Healthcare Corporation, Roche Pharma AG
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1. Study Identification

Unique Protocol Identification Number
NCT00205556
Brief Title
Effect of Increased Convective Clearance by On-Line Hemodiafiltration on All Cause Mortality in Chronic Hemodialysis Patients
Acronym
CONTRAST
Official Title
Effect of Increased Convective Clearance by On-line Hemodiafiltration on All Cause and Cardiovascular Mortality in Chronic Hemodialysis Patients: The Dutch Convective Transport Study (CONTRAST)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2011
Overall Recruitment Status
Completed
Study Start Date
June 2004 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
January 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Amsterdam UMC, location VUmc
Collaborators
UMC Utrecht, Medical Center Alkmaar, Maasstad Hospital, Julius Center for Health Sciences and Primary Care, Utrecht, Dutch Kidney Foundation, Fresenius Medical Care North America, Gambro Renal Products, Inc., Baxter Healthcare Corporation, Roche Pharma AG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare the effect of low flux hemodialysis with online hemodiafiltration on all cause mortality and a combination of cardiovascular morbidity and mortality in chronic hemodialysis patients.
Detailed Description
Today, an increasing number of patients with chronic renal failure (CRF) is treated with (on-line) hemodiafiltration (HDF). This practice is based on the assumption that the high incidence of cardiovascular (CV) disease, as observed in patients with CRF, is at least partially related to the retention of uremic toxins in the middle and large-middle molecular (MM) range. As HDF lowers these molecules more effectively than HD, it has been suggested that this treatment improves CV outcome, if compared to standard HD. Thus far, no definite data on the effects of HDF on CV parameters and/or clinical end-points are available. Promising data include a reduction of left ventricular mass index (LVMi) after one year of treatment with acetate free bio-filtration (AFB). Furthermore, relatively high survival rates were reported in a single center non-experimental study on patients who were treated with HDF, if compared to the EDTA registry data on HD-treated patients. Yet, these data are of observational nature, with the possibility of being biased by confounding by indication. As the accumulation of MMW substances has been implicated in increased oxidative stress and endothelial dysfunction, a reduction of these compounds might improve these derangements. In addition, cardiac dysfunction, atherosclerosis (as measured by left ventricular mass index [LVMi], carotid intima media thickness [CIMT]) and vascular stiffness (as measured by pulse wave velocity [PWV]) might be reduced during HDF, as compared to low-flux HD. Therefore, we propose a prospective, randomized multicenter trial, comparing (on-line) HDF with HD. After a stabilization period, an expected number of 700 chronic HD patients will be randomized to either HDF or low-flux HD and followed during 1-6 years. Primary end points are all cause mortality and combined CV events and mortality. In addition, LVMi, PWV, CIMT and various parameters of oxidative stress, acute phase reaction (APR) and endothelial function will be assessed and compared between treatment groups. This study will provide strong evidence on the efficacy of HDF compared to low flux HD on CV morbidity and mortality, which is currently lacking but urgently needed. It is highly likely that the outcome of this study will affect current clinical practice considerably, in the Netherlands as well as internationally. Moreover, the study will point towards the mechanisms underlying the effects of HDF. The following hypotheses will be tested: All-cause mortality and combined CV morbidity and mortality in patients treated with (on-line) HDF is lower than in patients treated with standard low-flux HD. A reduction in MMW uremic toxins by HDF leads to an improvement of the 'uremic profile' (as measured by AGE-levels, homocysteine levels, oxidative stress, and endothelial dysfunction), if compared to standard low-flux HD. The improvement of the 'uremic profile' in HDF-treated patients results in an improvement of endothelial function with a reduction in the progression of vascular injury (as measured by CIMT and PWV) and a reduction in LVMi, if compared to standard low-flux HD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Renal Disease, Cardiovascular Disease
Keywords
online hemodiafiltration, low flux hemodialysis, cardiovascular disease, endothelial dysfunction, uremic toxicity, quality of life, nutritional status

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1: low flux hemodialysis
Arm Type
Other
Arm Description
standard treatment
Arm Title
2 on-line hemodiafiltration
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
on-line hemodiafiltration
Intervention Description
addition of convective transport to regular dialysis treatment by using on-line hemodiafiltration
Intervention Type
Procedure
Intervention Name(s)
low flux hemodialysis
Intervention Description
standard treatment
Primary Outcome Measure Information:
Title
all cause mortality
Time Frame
entire follow up (until dead or end of study, 1-7 years)
Secondary Outcome Measure Information:
Title
fatal and non-fatal cardiovascular events
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
Left ventricular mass index (LVMi), carotid IMT (intima media thickness), aortic pulse wave velocity (PWV)
Time Frame
first 3 years
Title
laboratory markers of endothelial dysfunction, micro-inflammation, oxidative stress
Time Frame
first three years of follow up
Title
lipid profiles, uremic toxins
Time Frame
first three years
Title
quality of life
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
nutritional state
Time Frame
entire follow up (until death or end of study 1-7 years)
Title
anemia management
Description
hemoglobin levels, erythropoietin use / resistance iron saturation / ferritin levels, prescription of iron medication
Time Frame
first 12 months of follow up
Title
cost utility analysis
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
hospital admissions
Description
hospitalization days hospital admission for infections hospital admission for any cause
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
blood pressure and antihypertensive medication
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
residual kidney function
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
mineral bone disease
Description
laboratory parameters of mineral bone disease and medication (phosphate binders, vitamin D (or analogues), cinacalet)
Time Frame
entire follow up (until death or end of study, 1-7 years)
Title
parameters of treatment / treatment delivery
Description
dialysis efficiency (Kt/V urea); bloodflow, dialysate flow, ultrafiltration volume, (HDF:) convection volume
Time Frame
entire follow up (until death or end of study, 1-7 years)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients treated by HD 2 or 3 times a week, for at least 2 months Patients able to understand the study procedures Patients willing to provide written informed consent Exclusion Criteria: Current age < 18 years Treatment by HDF or high flux HD in the preceding 6 months Severe incompliance (severe non-adherence to the dialysis procedure and accompanying prescriptions, especially frequency and duration of dialysis treatment and fluid restriction) Life expectancy < 3 months due to non renal disease Participation in other clinical intervention trials evaluating cardiovascular outcome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Menso J Nubé, MD PhD
Organizational Affiliation
Medical Center Alkmaar
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Piet M ter Wee, MD PhD
Organizational Affiliation
Vrije Universiteit Medical Center, Amsterdam
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Peter J Blankestijn, MD PhD
Organizational Affiliation
Universityr Medical Center Utrecht
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
René A van den Dorpel, MD PhD
Organizational Affiliation
Medisch Centrum Rijnmond Zuid - locatie Clara, Rotterdam
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Michiel L Bots, MD PhD
Organizational Affiliation
Julius Center for Health Sciences and Primary Care, Utrecht
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Muriel PC Grooteman, MD PhD
Organizational Affiliation
Vrije Universiteit Medical Center, Amsterdam
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr Georges-L. Dumont Regional Hospital
City
Moncton
State/Province
New Brunswick
Country
Canada
Facility Name
Centre Hospitalier de L'Université de Montreal, Hopital Notre Dame
City
Montreal
ZIP/Postal Code
H2L 4M1
Country
Canada
Facility Name
Jeroen Bosch Ziekenhuis
City
's Hertogenbosch
ZIP/Postal Code
5200 ME
Country
Netherlands
Facility Name
Medisch Centrum Alkmaar
City
Alkmaar
ZIP/Postal Code
1815 JD
Country
Netherlands
Facility Name
Vrije Universiteit Medisch Centrum
City
Amsterdam
ZIP/Postal Code
1081 HV
Country
Netherlands
Facility Name
Onze Lieve Vrouwe Gasthuis
City
Amsterdam
ZIP/Postal Code
1090 HM
Country
Netherlands
Facility Name
Academical Medical Center
City
Amsterdam
ZIP/Postal Code
1100 DD
Country
Netherlands
Facility Name
Ziekenhuis Rijnstate
City
Arnhem
ZIP/Postal Code
6800 TA
Country
Netherlands
Facility Name
Dialyse Kliniek Noord
City
Beilen
ZIP/Postal Code
9411 SE
Country
Netherlands
Facility Name
Haga Ziekenhuis (locatie Leyenburg)
City
Den Haag
ZIP/Postal Code
2545 CH
Country
Netherlands
Facility Name
Slingeland Ziekenhuis
City
Doetinchem
ZIP/Postal Code
7009 BL
Country
Netherlands
Facility Name
Ziekenhuis Gelderse Vallei
City
Ede
ZIP/Postal Code
6710 HN
Country
Netherlands
Facility Name
Catharina Ziekenhuis
City
Eindhoven
ZIP/Postal Code
5602 ZA
Country
Netherlands
Facility Name
Oosterscheldeziekenhuis
City
Goes
ZIP/Postal Code
4460 BB
Country
Netherlands
Facility Name
Groene Hart Ziekenhuis
City
Gouda
Country
Netherlands
Facility Name
Martini Ziekenhuis
City
Groningen
ZIP/Postal Code
9700 RM
Country
Netherlands
Facility Name
Rijnland Ziekenhuis
City
Leiderdorp
Country
Netherlands
Facility Name
University Medical Center St Radboud
City
Nijmegen
ZIP/Postal Code
6500 HB
Country
Netherlands
Facility Name
Franciscus Ziekenhuis
City
Roosendaal
ZIP/Postal Code
4700 AZ
Country
Netherlands
Facility Name
Sint Franciscus Gasthuis
City
Rotterdam
ZIP/Postal Code
3045 PM
Country
Netherlands
Facility Name
Medisch Centrum Rijnmond Zuid - locatie Clara
City
Rotterdam
ZIP/Postal Code
3075 EA
Country
Netherlands
Facility Name
Orbis Medisch en Zorgcentrum
City
Sittard
ZIP/Postal Code
6130 MB
Country
Netherlands
Facility Name
Ziekenhuis Zeeuws-Vlaanderen
City
Terneuzen
ZIP/Postal Code
4535 PA
Country
Netherlands
Facility Name
St Elisabeth Ziekenhuis
City
Tilburg
ZIP/Postal Code
5000 LC
Country
Netherlands
Facility Name
Stichting Dianet
City
Utrecht
ZIP/Postal Code
3524 BN
Country
Netherlands
Facility Name
University Medical Center Utrecht
City
Utrecht
ZIP/Postal Code
3584 CX
Country
Netherlands
Facility Name
VieCuri Medisch Centrum
City
Venlo
ZIP/Postal Code
5912 BL
Country
Netherlands
Facility Name
Isala Klinieken
City
Zwolle
ZIP/Postal Code
8000 GM
Country
Netherlands
Facility Name
Haukeland Universitetssykehus
City
Bergen
ZIP/Postal Code
5021
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
15907201
Citation
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Results Reference
background
PubMed Identifier
15663765
Citation
Penne EL, Blankestijn PJ, Bots ML, van den Dorpel MA, Grooteman MP, Nube MJ, ter Wee PM; CONTRAST Group. Resolving controversies regarding hemodiafiltration versus hemodialysis: the Dutch Convective Transport Study. Semin Dial. 2005 Jan-Feb;18(1):47-51. doi: 10.1111/j.1525-139X.2005.18107.x.
Results Reference
background
PubMed Identifier
16886698
Citation
Penne EL, Blankestijn PJ, Bots ML, van den Dorpel MA, Grooteman MP, Nube MJ, ter Wee PM. [New study evaluating online haemodiafiltration for the reduction of cardiovascular morbidity and mortality in patients undergoing chronic haemodialysis]. Ned Tijdschr Geneeskd. 2006 Jul 15;150(28):1583-5. Dutch.
Results Reference
background
PubMed Identifier
18045819
Citation
van der Weerd NC, Penne EL, van den Dorpel MA, Grooteman MP, Nube MJ, Bots ML, ter Wee PM, Blankestijn PJ. Haemodiafiltration: promise for the future? Nephrol Dial Transplant. 2008 Feb;23(2):438-43. doi: 10.1093/ndt/gfm791. Epub 2007 Nov 28. No abstract available.
Results Reference
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PubMed Identifier
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Citation
Penne EL, van Berkel T, van der Weerd NC, Grooteman MP, Blankestijn PJ. Optimizing haemodiafiltration: tools, strategy and remaining questions. Nephrol Dial Transplant. 2009 Dec;24(12):3579-81. doi: 10.1093/ndt/gfp333. Epub 2009 Jul 13. No abstract available.
Results Reference
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PubMed Identifier
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Citation
van der Weerd NC, Penne EL, Grooteman MP. Effect of hemofiltration on mortality: no definite answer yet. Am J Kidney Dis. 2009 Mar;53(3):562-3; author reply 563. doi: 10.1053/j.ajkd.2008.09.029. No abstract available.
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Effect of Increased Convective Clearance by On-Line Hemodiafiltration on All Cause Mortality in Chronic Hemodialysis Patients

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