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Collaborative Research on HFR High Flux (SALATO)

Primary Purpose

Inflammation

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
SUPRA-HFR
Sponsored by
Azienda Sanitaria Locale di Cagliari
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammation focused on measuring SUPRA-HFR, adsorpition, vitamins, large toxins

Eligibility Criteria

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

Inclusion Criteria:

  • dialysis vintage > 6 months
  • well functioning vascular access (QB > 300 mL/min)
  • informed consent given

Exclusion Criteria:

  • polycystic kidney disease (PKD)
  • significant acute or chronic inflammatory comorbidities
  • non-renal related anemia
  • blood transfusions in the last 2 months before enrollment
  • alcohol or drugs abuse
  • malignant neoplasm
  • hemoglobinopathy or myelopathy
  • pregnancy

Sites / Locations

  • Territorial dialysis service, Regional Health system nephrology and dialysis department
  • Nephrology and dialysis, SS. Trinità Hospital
  • Nephrology and dialysis, Civil Hospital
  • Nephrology and dialysis, Civil Hospital
  • Nephrology and dialysis department, Versilia Hospital
  • Nephrology and dialysis department, Civil Hospital
  • Nephrology and dialysis, San Francesco Hospital
  • Nephrology and dialysis, San Martino Hospital
  • Nephrology and dialysis department, Bonaria Hospital
  • Nephrology and dialysis, San Camillo Hospital
  • Nephrology and dialysis, Dettori Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

standard HFR therapy

SUPRA-HFR therapy

Arm Description

standard HFR hemodiafiltration therapy

SUPRA-HFR hemodiafiltration therapy

Outcomes

Primary Outcome Measures

selective depuration of large uraemic toxins and reduction of nutrient losses
evaluation of the serum level of albumin, antioxidant vitamins and cytokines (IL6, IL1-beta)

Secondary Outcome Measures

amelioration of the anemia management
evaluation of ESAs dose, Hb level

Full Information

First Posted
December 10, 2011
Last Updated
June 13, 2016
Sponsor
Azienda Sanitaria Locale di Cagliari
Collaborators
Bellco s.r.l., Istituto Superiore di Sanità
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1. Study Identification

Unique Protocol Identification Number
NCT01492491
Brief Title
Collaborative Research on HFR High Flux
Acronym
SALATO
Official Title
Collaborative Study on Outcome of Antioxidant Vitamines, Microinflammation Parameters and Middle-high Toxins in ESRD Patients Treated With Online HDF, HFR and SUPRA-HFR
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
March 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Sanitaria Locale di Cagliari
Collaborators
Bellco s.r.l., Istituto Superiore di Sanità

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the serum concentrations of antoxidant vitamines A, C, E, inflammatory cytokines and middle-large toxins in patients treated with online hemodiafiltration, standard HFR and SUPRA-HFR.
Detailed Description
Today, as the research work of EUTOX group highlights, large cytokines and protein-bound solutes are gaining a relevant attention because of their emerging role as mortality predictors. Online hemodiafiltration (online HDF) has demonstrated to offer a significant depuration for small and middle toxins, but removal of protein-bound solutes is scarce. Synthetic high-flux membranes do not allow infact significant removal of molecules heavier than 15-20 KDa. Super-flux membranes may enhance online HDF convective transport but it would surely expose the patient to unacceptable losses of albumin, vitamines and aminoacids because of the non selectivity of the convective transport. HFR is a renal replacement therapy that utilizes convection, diffusion and adsorption. It uses a double-stage filter that consists of a high-flux polyethersulfone hemofilter in the first convective stage and a low-flux polyethersulfone filter in the second diffusive stage. The stages of the filter allow complete separation of convection from diffusion. The convective part of the first stage allows pure ultrafiltrate (UF) to pass through a sorbent resin cartridge. The first convective/adsorption stage has no net fluid removal. The blood and reinfused clean UF then undergo traditional dialysis. The second stage works by classicaHD and in this final stage the weight loss occurs. HFR has demonstrated in various clinical trials to reduce the microinflammatory state with no albumin loss and minimal aminoacids losses, thanks to the high selectivity of the resin sorbent. SUPRA-HFR is a newly developed HDF therapy based on the HFR concept scheme, which includes a super-flux membrane in the first section, coupled with an empowered resin sorbent. This should significantly enhance large solutes depuration, overcoming online HDF flaws. Therefore we proposed a prospective, multicenter, randomized study comparing online HDF, standard HFR and SUPRA-HFR. After a wash-out stabilization period of 4 months in post-dilution online HDF, an expected number of 50 patients will be randomized either in standard HFR (25) or in SUPRA-HFR (25) and followed for 6 months. Primary end points focus on the the removal of protein-bound solutes, inflammation and nutritional state. In addition, ESAs doses and hemoglobin levels will be assessed and compared between treatment groups. This study will provide strong evidence on the safe and clinically effective use of super-flux membranes, introduced with SUPRA-HFR therapy. It is highly likely that the outcomes of this study will affect the daily clinical practice of Italian and European dialysis centers because of the potential innovation brought to the market. The following hypotheses will be tested: SUPRA-HFR selectivity will reduce consistently the albumin, aminoacids and vitamines A, C, E losses compared to online HDF. SUPRA-HFR better preservation of the nutritional parameters, coupled with the possibility to remove protein-bound toxins and cytokines should lead to a higher reduction of the microinflammatory status, compared to online HDF and to standard HFR. SUPRA-HFR impact on inflammation status should ameliorate the anemia management by reducing the administered ESAs doses.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammation
Keywords
SUPRA-HFR, adsorpition, vitamins, large toxins

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
standard HFR therapy
Arm Type
No Intervention
Arm Description
standard HFR hemodiafiltration therapy
Arm Title
SUPRA-HFR therapy
Arm Type
Active Comparator
Arm Description
SUPRA-HFR hemodiafiltration therapy
Intervention Type
Device
Intervention Name(s)
SUPRA-HFR
Intervention Description
usual dialytic prescription for duration, frequency, acid buffer and anticoagulation regimen.
Primary Outcome Measure Information:
Title
selective depuration of large uraemic toxins and reduction of nutrient losses
Description
evaluation of the serum level of albumin, antioxidant vitamins and cytokines (IL6, IL1-beta)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
amelioration of the anemia management
Description
evaluation of ESAs dose, Hb level
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: dialysis vintage > 6 months well functioning vascular access (QB > 300 mL/min) informed consent given Exclusion Criteria: polycystic kidney disease (PKD) significant acute or chronic inflammatory comorbidities non-renal related anemia blood transfusions in the last 2 months before enrollment alcohol or drugs abuse malignant neoplasm hemoglobinopathy or myelopathy pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Piergiorgio Bolasco, MD
Organizational Affiliation
Azienda Sanitaria Locale di Cagliari
Official's Role
Principal Investigator
Facility Information:
Facility Name
Territorial dialysis service, Regional Health system nephrology and dialysis department
City
Cagliari
ZIP/Postal Code
09045
Country
Italy
Facility Name
Nephrology and dialysis, SS. Trinità Hospital
City
Cagliari
ZIP/Postal Code
09132
Country
Italy
Facility Name
Nephrology and dialysis, Civil Hospital
City
La Maddalena
ZIP/Postal Code
07024
Country
Italy
Facility Name
Nephrology and dialysis, Civil Hospital
City
Lanusei
ZIP/Postal Code
08045
Country
Italy
Facility Name
Nephrology and dialysis department, Versilia Hospital
City
Lido di Camaiore
ZIP/Postal Code
55041
Country
Italy
Facility Name
Nephrology and dialysis department, Civil Hospital
City
Macomer
ZIP/Postal Code
08015
Country
Italy
Facility Name
Nephrology and dialysis, San Francesco Hospital
City
Nuoro
ZIP/Postal Code
08100
Country
Italy
Facility Name
Nephrology and dialysis, San Martino Hospital
City
Oristano
ZIP/Postal Code
09170
Country
Italy
Facility Name
Nephrology and dialysis department, Bonaria Hospital
City
San Gavino Monreale
ZIP/Postal Code
09037
Country
Italy
Facility Name
Nephrology and dialysis, San Camillo Hospital
City
Sorgono
ZIP/Postal Code
08038
Country
Italy
Facility Name
Nephrology and dialysis, Dettori Hospital
City
Tempio
ZIP/Postal Code
07029
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
17684347
Citation
Wratten ML, Ghezzi PM. Hemodiafiltration with endogenous reinfusion. Contrib Nephrol. 2007;158:94-102. doi: 10.1159/000107239.
Results Reference
background
PubMed Identifier
21242676
Citation
Bolasco PG, Ghezzi PM, Serra A, Corazza L, Murtas S, Mascia M, Cossu M, Ferrara R, Cogoni G, Cadinu F, Casu D, Contu B, Passaghe M, Ghisu T, Ganadu M, Logias F. Hemodiafiltration with endogenous reinfusion with and without acetate-free dialysis solutions: effect on ESA requirement. Blood Purif. 2011;31(4):235-42. doi: 10.1159/000322400. Epub 2011 Jan 14.
Results Reference
background
PubMed Identifier
16303780
Citation
Panichi V, Manca-Rizza G, Paoletti S, Taccola D, Consani C, Filippi C, Mantuano E, Sidoti A, Grazi G, Antonelli A, Angelini D, Petrone I, Mura C, Tolaini P, Saloi F, Ghezzi PM, Barsotti G, Palla R. Effects on inflammatory and nutritional markers of haemodiafiltration with online regeneration of ultrafiltrate (HFR) vs online haemodiafiltration: a cross-over randomized multicentre trial. Nephrol Dial Transplant. 2006 Mar;21(3):756-62. doi: 10.1093/ndt/gfi189. Epub 2005 Nov 22.
Results Reference
background
PubMed Identifier
27566671
Citation
Palleschi S, Ghezzi PM, Palladino G, Rossi B, Ganadu M, Casu D, Cossu M, Mattana G, Pinna AM, Contu B, Ghisu T, Monni A, Gazzanelli L, Mereu MC, Logias F, Passaghe M, Amore A, Bolasco P; Sardinian Study Group. Vitamins (A, C and E) and oxidative status of hemodialysis patients treated with HFR and HFR-Supra. BMC Nephrol. 2016 Aug 26;17(1):120. doi: 10.1186/s12882-016-0315-6.
Results Reference
derived

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Collaborative Research on HFR High Flux

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