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Combination of Medium Cut-off Dialyzer Membrane and Diet Modification to Alleviate Residual Uremic Syndrome of Dialysis Patients

Primary Purpose

End Stage Renal Disease, Haemodialysis, Diet, Healthy

Status
Recruiting
Phase
Not Applicable
Locations
Slovenia
Study Type
Interventional
Intervention
medium cut-off (MCO) dialysis membrane
Dietary fiber mixture (Plantago Psyllium and Inulin)
Sodium propionate
Sponsored by
University Medical Centre Ljubljana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End Stage Renal Disease focused on measuring medium cut-off dialysis membrane, p-cresol sulphate, indoxyl-sulphate, trimethylamine-N-oxide (TMAO), hemodiafiltration, uremic toxins, dietary fibre, end stage renal disease

Eligibility Criteria

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

Inclusion Criteria:

  • patient on chronic hemodialysis or hemodiafiltration for at least 12 weeks,
  • age 18 years old or more,
  • a functioning arteriovenous fistula or graft as a permanent dialysis vascular access,
  • being able to give an informed consent to participate in the survey;

Exclusion Criteria:

  • planned kidney transplantation, transition to peritoneal dialysis or to another dialysis center within 12 weeks of the start of the study,
  • active chronic inflammation (e.g., an active autoimmune disease or an open wound), chronic ongoing infection or cancer in last 4 weeks,
  • acute febrile illness in last 4 weeks,
  • new cardiovascular or neurovascular event in last 4 weeks,
  • a need for hospitalization in the last 4 weeks,
  • clinically evident malnutrition and/or body mass index of 19 kg/m2 and/or loss of body weight for 5% in last 3 months,
  • immunosuppressive treatment,
  • expected survival of less than 1 year,
  • pregnancy or breast-feeding,
  • indication for dietary supplements to increase calorie and / or protein intake,
  • specific indication for carrying out hemodiafiltration instead of hemodialysis as per attending physician,
  • serum albumin concentration <32 g/l at screening to enter the study,
  • inability to follow the study diet or test procedures,
  • rapid reduction of residual renal function in the period prior to entry into the study,
  • intolerant of on-line haemodiafiltration (infusion intolerance);

Sites / Locations

  • University Medical Center ljubljanaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Interventional arm - MCO dialysis membrane

Control arm - high-flux membrane haemodiafiltration

Arm Description

4 weeks of dialysis with MCO (Theranova) membrane then dialysis for 4 weeks with MCO membrane and increased fiber intake

4 weeks of high-flux membrane haemodiafiltration and 4 weeks of high-flux membrane haemodiafiltration and increased fiber intake

Outcomes

Primary Outcome Measures

Serum concentration of uremic toxin p-cresol sulphate
Blood for the laboratory measurements of serum total p-cresol sulphate concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.

Secondary Outcome Measures

Serum concentration of uremic toxins indoxyl sulfate
Blood for the laboratory measurements of serum total indoxyl sulfate concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.

Full Information

First Posted
January 28, 2020
Last Updated
May 17, 2022
Sponsor
University Medical Centre Ljubljana
Collaborators
University of Ljubljana
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1. Study Identification

Unique Protocol Identification Number
NCT04247867
Brief Title
Combination of Medium Cut-off Dialyzer Membrane and Diet Modification to Alleviate Residual Uremic Syndrome of Dialysis Patients
Official Title
Combination of Medium Cut-off Dialyzer Membrane and Diet Modification to Alleviate Residual Uremic Syndrome of Dialysis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 31, 2020 (Actual)
Primary Completion Date
August 30, 2022 (Anticipated)
Study Completion Date
October 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Centre Ljubljana
Collaborators
University of Ljubljana

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study will compare achieved levels of protein-bound uremic toxins with dialysis using a medium cut-off membrane compared to the treatment by online haemodiafiltration with a high-flux dialysis membrane. In the second phase of the study dietary fiber and short-chain fatty acid intake will be increased to verify a possible additional reduction in the levels of protein bound uremic toxins.
Detailed Description
The investigators will carry out a prospective interventional randomised study to compare achieved serum concentrations of selected protein bound uremic toxins by dialysis with a medium cut-off membrane (Theranova, Baxter AG, USA) and online hemodiafiltration with a standard "high-flux" dialysis membrane. In the second phase, both dialysis purification methods will be supplemented by a change in the diet with increase of the daily intake of dietary fiber to 30g and addition of a short-chain fatty acid propionate in the dose of 1 g daily. The main outcome of the study is the serum concentration of p-cresol sulphate. Secondary outcome is the serum concentration of indoxyl-sulphate and trimethylamine-N-oxide (TMAO). Serum albumin concentration and lean body weight of patients represent safety outcomes for this study. This investigator-initiated research project has been entirely planned and will be conducted by the clinical researchers in a tertiary University Medical Center Ljubljana. The study will include 50 chronic prevalent stable dialysis patients in the following periods: 2 weeks of wash-in period with standard bicarbonate haemodialysis and standard high-flux dialysis membrane, then the patients will be randomized in a 1:1 ratio to either one of the two study arms: (interventional study arm) 4 weeks of dialysis with medium cut-off (Theranova) membrane (first phase), then dialysis for 4 weeks with the same membrane and increased fiber intake (second phase), (control study arm) 4 weeks of dialysis with a high-flux membrane using on-line haemodiafiltration (first phase) and 4 weeks of high-flux membrane haemodiafiltration and increased fiber intake (second phase), finally, all patients will undergo a 4 week wash-out period with a standard bicarbonate haemodialysis using standard high-flux dialysis membrane identical to wash-in period. Measurement of the study end-points will be carried out at the end of 2-week wash-in period, each 4-week period and at the end of 4 week wash-out period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease, Haemodialysis, Diet, Healthy
Keywords
medium cut-off dialysis membrane, p-cresol sulphate, indoxyl-sulphate, trimethylamine-N-oxide (TMAO), hemodiafiltration, uremic toxins, dietary fibre, end stage renal disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a prospective, randomized, interventional, two parallel arm study.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Interventional arm - MCO dialysis membrane
Arm Type
Experimental
Arm Description
4 weeks of dialysis with MCO (Theranova) membrane then dialysis for 4 weeks with MCO membrane and increased fiber intake
Arm Title
Control arm - high-flux membrane haemodiafiltration
Arm Type
Active Comparator
Arm Description
4 weeks of high-flux membrane haemodiafiltration and 4 weeks of high-flux membrane haemodiafiltration and increased fiber intake
Intervention Type
Device
Intervention Name(s)
medium cut-off (MCO) dialysis membrane
Other Intervention Name(s)
Theranova dialysis membrane (Baxter AG)
Intervention Description
Medium cut-off dialysis (MCO) membrane is a dialysis membrane with a higher molecular weight retention onset and similar cut-off as standard high-flux dialysis membranes. It is capable of providing increased clearance of medium sized uremic toxins and some plasma proteins (cytokines, inflammatory mediators).
Intervention Type
Dietary Supplement
Intervention Name(s)
Dietary fiber mixture (Plantago Psyllium and Inulin)
Other Intervention Name(s)
Kolon3aktiv fiber powder (manufacturer TOPNATUR s.r.o., Czech republic)
Intervention Description
Dietary fiber (Psyllium 69% and Inulin 30% mixture) added to the meals in the dose of 5g BID for 4 weeks in the second phase of the study.
Intervention Type
Dietary Supplement
Intervention Name(s)
Sodium propionate
Intervention Description
Sodium propionate (a short-chain fatty acid) added to the meals in the dose of 500 mg BID in the second phase in the study.
Primary Outcome Measure Information:
Title
Serum concentration of uremic toxin p-cresol sulphate
Description
Blood for the laboratory measurements of serum total p-cresol sulphate concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Secondary Outcome Measure Information:
Title
Serum concentration of uremic toxins indoxyl sulfate
Description
Blood for the laboratory measurements of serum total indoxyl sulfate concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Other Pre-specified Outcome Measures:
Title
Serum concentration of uremic toxin trimethylamine N-oxide (TMAO)
Description
Blood for the laboratory measurements of serum TMAO concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Serum concentration of beta2-microglobulin
Description
Blood for the laboratory measurements of serum beta2-microglobulin concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Serum concentration of phosphate
Description
Blood for the laboratory measurements of serum phosphate concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Serum urea concentration
Description
Blood for the laboratory measurements of serum urea concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Serum albumin concentration
Description
Blood for the laboratory measurements of serum albumin concentration will be taken from the arterial line before the start of midweek hemodialysis procedure.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Dialysis symptom index questionnaire score
Description
A validated questionnaire of 30 questions regarding the dialysis symptoms experienced during the last week. Unabbreviated scale title: Dialysis symptom index. Each of 30 items (symptoms) is ranked on a 5-point Likert scale. Minimal score: 0. Maximum score: 150. Higher scores mean worse outcomes (worse symptom burden).
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Time to finish 10 repetition sit to stand test
Description
This validated test measures lower limb strength. Participants are required to stand up and sit down 10 times from an armless chair as quickly as possible, the outcome is the time needed to perform the test.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of first phase (4 weeks after baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).
Title
Physical activity level as measured by accelerometry
Description
Number of accelerometer counts in 7 days.
Time Frame
At the end of wash-in period (basal sample-baseline), at the end of second phase (8 weeks after baseline), at the end of wash-out period (12 weeks after baseline).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patient on chronic hemodialysis or hemodiafiltration for at least 12 weeks, age 18 years old or more, a functioning arteriovenous fistula or graft as a permanent dialysis vascular access, being able to give an informed consent to participate in the survey; Exclusion Criteria: planned kidney transplantation, transition to peritoneal dialysis or to another dialysis center within 12 weeks of the start of the study, active chronic inflammation (e.g., an active autoimmune disease or an open wound), chronic ongoing infection or cancer in last 4 weeks, acute febrile illness in last 4 weeks, new cardiovascular or neurovascular event in last 4 weeks, a need for hospitalization in the last 4 weeks, clinically evident malnutrition and/or body mass index of 19 kg/m2 and/or loss of body weight for 5% in last 3 months, immunosuppressive treatment, expected survival of less than 1 year, pregnancy or breast-feeding, indication for dietary supplements to increase calorie and / or protein intake, specific indication for carrying out hemodiafiltration instead of hemodialysis as per attending physician, serum albumin concentration <32 g/l at screening to enter the study, inability to follow the study diet or test procedures, rapid reduction of residual renal function in the period prior to entry into the study, intolerant of on-line haemodiafiltration (infusion intolerance);
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jernej Pajek, MD, PhD
Phone
+38615228124
Email
jernej.pajek@mf.uni-lj.si
First Name & Middle Initial & Last Name or Official Title & Degree
Tjaša Herič, MD
Phone
+38615228964
Ext
+38670861169
Email
tjasa.heric@kclj.si
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jernej Pajek, MD, PhD
Organizational Affiliation
Nephrology department, University Medical Centre Ljubljana, Slovenia
Official's Role
Study Chair
Facility Information:
Facility Name
University Medical Center ljubljana
City
Ljubljana
ZIP/Postal Code
1000
Country
Slovenia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jernej Pajek, MD, pHD
Phone
+38615228124
Email
jernej.pajek@mf.uni-lj.si

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Plan to share IPD that underline results published in the manuscripts reporting study results.
IPD Sharing Time Frame
From the time of publication of associated manuscripts for 10 years.
IPD Sharing Access Criteria
Available on demand from the investigators.
Citations:
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Citation
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Combination of Medium Cut-off Dialyzer Membrane and Diet Modification to Alleviate Residual Uremic Syndrome of Dialysis Patients

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