Mid-HDF Randomized Controlled Study on Outcome (MILESTONE)
Primary Purpose
End Stage Renal Disease
Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Mid-dilution HDF
HF dialysis
Sponsored by
About this trial
This is an interventional treatment trial for End Stage Renal Disease focused on measuring dialysis, mortality, cardiovascular stability, inflammation, quality of life
Eligibility Criteria
Inclusion Criteria:
- On a thrice/week RRT for at least 3 months
- Dialysis vintage > 3 months
- Signed informed consent
- Blood flow > 300 mL/min
Exclusion Criteria:
- On waiting list for living-donor transplant
- Residual diuresis > 500 mL/day
- Inability, as judget by the investigator, to follow or understand the protocol instructions
- Active neoplastic disease
- Single needle treatment
- Patients with expectancy life lower than 6 months
- Inclusion to other studies
- Pregnancy
Sites / Locations
- Cliniques Universitaires Saint-Luc
- Hôpital de la Conception
- Azienda Ospedaliero-Universitaria di Bologna
- Hospital Clínic Barcelona
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
HF dialysis
Mid-dilution HDF
Arm Description
HF (high-flux) dialysis is standard hemodialysis treatment performed by using a high permeability dialyzer instead of a low permeability one.
Mid-dilution is a newly developed hemodiafiltration therapy able to allow a simultaneous pre- and post-dilution infusion.
Outcomes
Primary Outcome Measures
crude, all-causes mortality
The primary objective will be assessed by the incidence rate of fatal events
Secondary Outcome Measures
Cardiovascular morbidity
It will be assessed by taking into consideration:
Number of hospital admissions related to non fatal major CV events
Length of stay during hospitalization
Quality of life and dialysis tolerance evaluated by questionnaire
It will be assessed by taking into consideration:
- Results of the SF-36 questionnaire given to the patients
Micro-inflammation evaluation
It will be assessed by measuring the pre-dialysis serum levels of:
IL-6 CR Myoglobin RbP p-cresylsulfate beta2-microglobulin.
The hospitals' laboratories will be in charge for the sample collection and analysis
Nutrition and anaemia management
It will be assessed by taking in consideration the pre-dialysis serum levels of:
Hb albumin iron.
ESAs and iron supplementation will be as well noted in apposite CRF.
Full Information
NCT ID
NCT01693354
First Posted
September 6, 2012
Last Updated
January 12, 2017
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
1. Study Identification
Unique Protocol Identification Number
NCT01693354
Brief Title
Mid-HDF Randomized Controlled Study on Outcome
Acronym
MILESTONE
Official Title
Mid-dilution Hemodiafiltration International Randomized Prospective Study on Incident Patients Focused on Outcome
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2012 (undefined)
Primary Completion Date
September 2017 (Anticipated)
Study Completion Date
September 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether mid-dilution hemodiafiltration is effective in the reduction of the crude mortality risk in patients who have been undergoing renal replacement treatment for less than 1 year. Patients will be randomized since the beginning of the study in two groups: standard HF dialysis and mid-dilution HDF.
Detailed Description
It is a matter of fact that in the last decades the Chronic Kidney Disease (CKD) population has widely changed. In Italy, for example, more than 50% of the incident dialysis patients are more than 70 year old, with diabetic and hypertension being the major underlying diseases; moreover a great percentage of the patients starts dialysis with a burden of at least 1-2 comorbidities [1]. Online hemodiafiltration (online HDF) has been recently associated with better patient survival in comparison with standard hemodialysis in two large trials [2,3]; the overall relative risk of mortality was found to be approximately 33% lower in patients treated with online HDF [2,3]. These impressive results were not obtained anyway on the whole population, but in a sub-group analysis. A strong correlation was found between the total convective volume obtained and the mortality risk reduction; HDF was found to be significantly better than standard hemodialysis when a total convective volume of 19-22 L/session (in 4 hours sessions of post-dilution HDF) was achieved.
These results support the importance of the "adequate convective dose" concept in order to improve the patient outcomes especially in frail patients, as recently demonstrated by a large randomised control trial, the MPO study [4], comparing High Flux versus Low Flux dialysis in patients with plasma albumin levels equal to or less than 4 gr/dl ( as a marker of patient comorbidities) and, in a post hoc analysis, in diabetic patients [4].
Mid-dilution HDF is a variant of classical HDF combining simultaneous pre- and post.-dilution in order to maximise middle and large solutes removal.
The MILESTONE study would aim to fully demonstrate for mid-dilution HDF the significant mortality risk reduction observed in the recent mentioned studies.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease
Keywords
dialysis, mortality, cardiovascular stability, inflammation, quality of life
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
500 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HF dialysis
Arm Type
Active Comparator
Arm Description
HF (high-flux) dialysis is standard hemodialysis treatment performed by using a high permeability dialyzer instead of a low permeability one.
Arm Title
Mid-dilution HDF
Arm Type
Experimental
Arm Description
Mid-dilution is a newly developed hemodiafiltration therapy able to allow a simultaneous pre- and post-dilution infusion.
Intervention Type
Device
Intervention Name(s)
Mid-dilution HDF
Other Intervention Name(s)
OLPUR MD 220, OLPUR MD 190
Intervention Description
Mid-dilution HDF is a special, newly developed variant of online HDF which is characterized by a dedicated high-flux hemodialyzer named OLPUR MD able to support simultaneous pre- and post-dilution
Intervention Type
Device
Intervention Name(s)
HF dialysis
Other Intervention Name(s)
PHYLTHER HF, DIAPES HF
Intervention Description
Standard hemodialyzers equipped with high permeability polyphenylene/polyethersulfone membranes
Primary Outcome Measure Information:
Title
crude, all-causes mortality
Description
The primary objective will be assessed by the incidence rate of fatal events
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Cardiovascular morbidity
Description
It will be assessed by taking into consideration:
Number of hospital admissions related to non fatal major CV events
Length of stay during hospitalization
Time Frame
5 years
Title
Quality of life and dialysis tolerance evaluated by questionnaire
Description
It will be assessed by taking into consideration:
- Results of the SF-36 questionnaire given to the patients
Time Frame
1 year
Title
Micro-inflammation evaluation
Description
It will be assessed by measuring the pre-dialysis serum levels of:
IL-6 CR Myoglobin RbP p-cresylsulfate beta2-microglobulin.
The hospitals' laboratories will be in charge for the sample collection and analysis
Time Frame
1 year
Title
Nutrition and anaemia management
Description
It will be assessed by taking in consideration the pre-dialysis serum levels of:
Hb albumin iron.
ESAs and iron supplementation will be as well noted in apposite CRF.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
On a thrice/week RRT for at least 3 months
Dialysis vintage > 3 months
Signed informed consent
Blood flow > 300 mL/min
Exclusion Criteria:
On waiting list for living-donor transplant
Residual diuresis > 500 mL/day
Inability, as judget by the investigator, to follow or understand the protocol instructions
Active neoplastic disease
Single needle treatment
Patients with expectancy life lower than 6 months
Inclusion to other studies
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco Maduell, MD
Organizational Affiliation
Hospital Clínic Barcelona, Spain
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Vincenzo Panichi, MD, PhD
Organizational Affiliation
AUSL 12 Viareggio, Italy
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Pedro Aljama, MD, PhD
Organizational Affiliation
Hospital Reina Sofia, Cordoba, Spain
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Michel Jadoul, MD, PhD
Organizational Affiliation
Cliniques Universitaires Saint-Luc, Brussels, Belgium
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Philippe Brunet, MD, PhD
Organizational Affiliation
Hôpital de la Conception, Marseille, France
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Antonio Santoro, MD
Organizational Affiliation
AOSP Bologna, Italy
Official's Role
Study Chair
Facility Information:
Facility Name
Cliniques Universitaires Saint-Luc
City
Brussels
ZIP/Postal Code
3000
Country
Belgium
Facility Name
Hôpital de la Conception
City
Marseille
ZIP/Postal Code
13385
Country
France
Facility Name
Azienda Ospedaliero-Universitaria di Bologna
City
Bologna
ZIP/Postal Code
40138
Country
Italy
Facility Name
Hospital Clínic Barcelona
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
12. IPD Sharing Statement
Citations:
PubMed Identifier
21245934
Citation
Stel VS, van de Luijtgaarden MW, Wanner C, Jager KJ; on behalf of the European Renal Registry Investigators. The 2008 ERA-EDTA Registry Annual Report-a precis. NDT Plus. 2011 Feb;4(1):1-13. doi: 10.1093/ndtplus/sfq191. Epub 2010 Nov 19.
Results Reference
background
PubMed Identifier
22539829
Citation
Grooteman MP, van den Dorpel MA, Bots ML, Penne EL, van der Weerd NC, Mazairac AH, den Hoedt CH, van der Tweel I, Levesque R, Nube MJ, ter Wee PM, Blankestijn PJ; CONTRAST Investigators. Effect of online hemodiafiltration on all-cause mortality and cardiovascular outcomes. J Am Soc Nephrol. 2012 Jun;23(6):1087-96. doi: 10.1681/ASN.2011121140. Epub 2012 Apr 26.
Results Reference
background
PubMed Identifier
16641921
Citation
Canaud B, Bragg-Gresham JL, Marshall MR, Desmeules S, Gillespie BW, Depner T, Klassen P, Port FK. Mortality risk for patients receiving hemodiafiltration versus hemodialysis: European results from the DOPPS. Kidney Int. 2006 Jun;69(11):2087-93. doi: 10.1038/sj.ki.5000447.
Results Reference
background
PubMed Identifier
19092122
Citation
Locatelli F, Martin-Malo A, Hannedouche T, Loureiro A, Papadimitriou M, Wizemann V, Jacobson SH, Czekalski S, Ronco C, Vanholder R; Membrane Permeability Outcome (MPO) Study Group. Effect of membrane permeability on survival of hemodialysis patients. J Am Soc Nephrol. 2009 Mar;20(3):645-54. doi: 10.1681/ASN.2008060590. Epub 2008 Dec 17.
Results Reference
background
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Mid-HDF Randomized Controlled Study on Outcome
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