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Theranova vs High-flux HD Comparison

Primary Purpose

End Stage Renal Failure on Dialysis

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
High-flux dialyzer
Theranova dialyzer
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End Stage Renal Failure on Dialysis

Eligibility Criteria

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

Inclusion Criteria:

  • adult patients age greater than 18 years old
  • end-stage renal failure on two- or three-times per week high-flux HD for more than 90 days
  • mean spKt/Vurea >1.2 per session (for 3 dialysis sessions per week) or spKt/Vurea >1.8 per session (for 2 dialysis sessions per week)

Exclusion Criteria:

  • active malignancy
  • unable to give informed consent or complete questionnaires
  • unstable clinical condition defined as significant clinical event requiring hospitalization in the past 90 days
  • unreliable vascular access
  • unable to achieve HD blood flow >150ml/min

Sites / Locations

  • Division of Nephrology, Department of Medicine, Queen Mary Hospital
  • Tung Wah Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Theranova

High-flux

Arm Description

Patients will be receiving hemodialysis using Theranova dialyzer. The other hemodialysis parameters are kept the same.

Patients will be receiving hemodialysis using a high-flux dialyzer. The other hemodialysis parameters are kept the same

Outcomes

Primary Outcome Measures

lean tissue index
measured by Body Composition Monitor
Body Mass Index
measured by weight (in kilograms) divided by the square of heights (in meters)

Secondary Outcome Measures

asymmetrical dimethylarginine
endogenous inhibitor of nitric oxide synthase, one of the cardiovascular biomarkers
fibroblast growth factor 23
biomarker for bone turnover
Klotho
biomarker for atherosclerosis and bone turnover
Kt/V urea
measurement of clearance of urea by hemodialysis therapy, a marker for adequacy of dialysis
beta-2 microglobulin
middle size uremic toxin
Pentraxin-3
middle to large molecular size uremic toxin
soluble endothelial protein C receptor
a marker for endothelial dysfunction
soluble thrombomodulin
a marker for endothelial dysfunction
hemoglobulin
indication of anemia
high-sensitive C reactive protein
marker for inflammation
interleukin 6
marker for inflammation
tumor necrosis factor alpha
marker for inflammation
albumin
marker for nutritional status
Leptin
marker for nutritional status and appetite
adiponectin
nutritional marker
phosphate
small size uremic waste produce
low-density lipoprotein
reflects lipid control
high-density lipoprotein
reflects lipid control
triglyceride
reflects lipid control
Malnutrition-Inflammation Score
a measurement scale reflecting nutritional status
Subjective Global Assesment questionnaire
a measurement scale reflecting nutritional status
fat tissue index
nutritional marker measured by Body Composition Monitor
admission rate due to cardiovascular events
number of admisisons due to cardiovascular events during the follow-up period
admission rate due to infection
number of admissions due to infection during the follow-up period
mortality rate
number of deaths during the follow-up period
5-D itch scale
Symptomatology scale to measure itchiness
Numeric rating scale for itchiness
Symptomatology scale to measure itchiness
The Functional Assessment of Anorexia/Cachexia Therapy (FAACT) score
measurement scale for appetite
Visual analogue scale for appetite
measurement scale for appetite
Postdialysis recovery time
number of time required to feel well after receiving a hemodialysis session
Self-reported sleep quality
scale to rate the quality of sleep
Hong Kong Montreal Cognitive Assessment
measurement of cognitive function
KDQOLSFTMv1.3 questionnaire
quality of life assessment
DNA methylation analysis of TRPV1 gene
epigenetics modification
DNA methylation analysis of LY96 gene
epigenetics modificaiton
DNA methylation analysis of IFNGR1 gene
epigenetics modifications

Full Information

First Posted
September 10, 2019
Last Updated
September 28, 2021
Sponsor
The University of Hong Kong
Collaborators
Baxter Healthcare Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT04106310
Brief Title
Theranova vs High-flux HD Comparison
Official Title
The Comparison of Expanded Dialysis With Theranova Dialyzer With Conventional High-flux Hemodialysis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
June 30, 2021 (Actual)
Study Completion Date
June 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
Collaborators
Baxter Healthcare Corporation

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
This research proposal of an investigator-initiated clinical study aims to examine the impact of uremic toxin removal afforded by middle cut-off (MCO) dialysis on clinical parameters and surrogate biomarkers pertinent to nutritional, systemic and vascular complications in dialysis patients. The primary research goal is to evaluate the outcomes indicative of nutritional status (as measured by body mass index, body composition monitoring, albumin, clinical assessments such as subjective global assessment, etc.) and parameters relevant to pathophysiological processes in uremia focusing on inflammation and cardiovascular risks. The secondary research aims are to examine dialysis efficacy between MCO dialysis and conventional hemodialysis (CHD). Specifically, dialysis efficacy will be determined by within and between subject differences in baseline versus short term (6 months) and long term (12 months) effects of MCO dialysis and CHD in: Removal of small molecules (e.g. urea), middle molecules (Beta-2 microglobulin, Phosphate and Creatinine) and protein bound solutes Markers of inflammation, ossification and fibrosis Uremia associated epigenetic modification The investigators hypothesize superiority of nutritional parameters in patients undergoing MCO dialysis compared with patients on CHD. The investigators plan to randomize 60 patients to either MCO dialysis or CHD at two hemodialysis units in Hong Kong.
Detailed Description
Accumulation of uremic toxins is associated morbidity and mortality in patients with end-stage renal disease, but the pathogenic mechanisms how they lead to various clinical complications remain elusive. Conventional hemodialysis is effective in removing small molecular solutes (in the range of 50-15,000 Da), but the removal of protein-bound and middle to larger molecular toxins (up to 50,000 Da) remains unsatisfactory even with augmented hemodialysis frequency or duration. The notion that dialysis adequacy is no longer a simple quantitative measure of small molecular removal has led to the clinical application of intensive hemodialysis and the search for novel strategies to reduce uremic toxin burden. Recently, a new class of membrane with molecular weight cut off (MWCO) close to the molecular weight of albumin was introduced. The focus of this new therapy, known as expanded dialysis using the medium cut off (MCO) dialysis membrane, is to provide the potential for more efficient removal of middle molecules and protein bound uremic toxins without excessive loss of albumin. To date, MCO dialysis has been associated with a reduction in transcription of pro-inflammatory cytokines (i.e. interleukin 6 and tumor necrosis factor-α) and middle molecules especially free lambda light chains. Protein-energy wasting and cardiovascular diseases are prevalent in chronic kidney disease and is related to inflammation and increased mortality. Despite growing data on the clearance of individual uremic toxins and biochemical parameters, the impact of MCO dialysis on clinical outcomes and mechanistic parameters related to nutrition and inflammation remains to be investigated. The objective of the study is to compare MCO dialysis with conventional high-flux HD, on nutritional parameters, inflammation and cardiovascular biomarkers and related clinical outcomes. Since twice-weekly HD is commonly practiced in Hong Kong, this study provides a distinct opportunity to investigate whether MCO dialysis might be particularly advantageous in patients receiving a relatively lower dialysis dose through the removal of a broader spectrum of uremic toxins. The investigators hypothesize that MCO dialysis with Theranova Dialyzer (HDx) improves parameters related to nutrition and inflammation compared with high-flux HD. This will be a prospective single-blinded, randomized, controlled trial with stable HD patients randomized at 1:1 ratio to either one of the following - A. to continue with HD using the same high-flux dialyzer as in the previous 6 weeks (high-flux HD arm) B. change to HDx using Theranova Dialyzer (MCO dialysis arm)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Failure on Dialysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
The dialyzer used will be covered
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Theranova
Arm Type
Active Comparator
Arm Description
Patients will be receiving hemodialysis using Theranova dialyzer. The other hemodialysis parameters are kept the same.
Arm Title
High-flux
Arm Type
Active Comparator
Arm Description
Patients will be receiving hemodialysis using a high-flux dialyzer. The other hemodialysis parameters are kept the same
Intervention Type
Device
Intervention Name(s)
High-flux dialyzer
Intervention Description
a dialyzer meeting the definition of high-flux
Intervention Type
Device
Intervention Name(s)
Theranova dialyzer
Intervention Description
a middle cut-off dialyzer
Primary Outcome Measure Information:
Title
lean tissue index
Description
measured by Body Composition Monitor
Time Frame
12 months
Title
Body Mass Index
Description
measured by weight (in kilograms) divided by the square of heights (in meters)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
asymmetrical dimethylarginine
Description
endogenous inhibitor of nitric oxide synthase, one of the cardiovascular biomarkers
Time Frame
12 months
Title
fibroblast growth factor 23
Description
biomarker for bone turnover
Time Frame
12 months
Title
Klotho
Description
biomarker for atherosclerosis and bone turnover
Time Frame
12 months
Title
Kt/V urea
Description
measurement of clearance of urea by hemodialysis therapy, a marker for adequacy of dialysis
Time Frame
12 months
Title
beta-2 microglobulin
Description
middle size uremic toxin
Time Frame
12 months
Title
Pentraxin-3
Description
middle to large molecular size uremic toxin
Time Frame
12 months
Title
soluble endothelial protein C receptor
Description
a marker for endothelial dysfunction
Time Frame
12 months
Title
soluble thrombomodulin
Description
a marker for endothelial dysfunction
Time Frame
12 months
Title
hemoglobulin
Description
indication of anemia
Time Frame
12 months
Title
high-sensitive C reactive protein
Description
marker for inflammation
Time Frame
12 months
Title
interleukin 6
Description
marker for inflammation
Time Frame
12 months
Title
tumor necrosis factor alpha
Description
marker for inflammation
Time Frame
12 months
Title
albumin
Description
marker for nutritional status
Time Frame
12 months
Title
Leptin
Description
marker for nutritional status and appetite
Time Frame
12 months
Title
adiponectin
Description
nutritional marker
Time Frame
12 months
Title
phosphate
Description
small size uremic waste produce
Time Frame
12 months
Title
low-density lipoprotein
Description
reflects lipid control
Time Frame
12 months
Title
high-density lipoprotein
Description
reflects lipid control
Time Frame
12 months
Title
triglyceride
Description
reflects lipid control
Time Frame
12 months
Title
Malnutrition-Inflammation Score
Description
a measurement scale reflecting nutritional status
Time Frame
12 months
Title
Subjective Global Assesment questionnaire
Description
a measurement scale reflecting nutritional status
Time Frame
12 months
Title
fat tissue index
Description
nutritional marker measured by Body Composition Monitor
Time Frame
12 months
Title
admission rate due to cardiovascular events
Description
number of admisisons due to cardiovascular events during the follow-up period
Time Frame
12 months
Title
admission rate due to infection
Description
number of admissions due to infection during the follow-up period
Time Frame
12 months
Title
mortality rate
Description
number of deaths during the follow-up period
Time Frame
12 months
Title
5-D itch scale
Description
Symptomatology scale to measure itchiness
Time Frame
12 months
Title
Numeric rating scale for itchiness
Description
Symptomatology scale to measure itchiness
Time Frame
12 months
Title
The Functional Assessment of Anorexia/Cachexia Therapy (FAACT) score
Description
measurement scale for appetite
Time Frame
12 months
Title
Visual analogue scale for appetite
Description
measurement scale for appetite
Time Frame
12 months
Title
Postdialysis recovery time
Description
number of time required to feel well after receiving a hemodialysis session
Time Frame
12 months
Title
Self-reported sleep quality
Description
scale to rate the quality of sleep
Time Frame
12 months
Title
Hong Kong Montreal Cognitive Assessment
Description
measurement of cognitive function
Time Frame
12 months
Title
KDQOLSFTMv1.3 questionnaire
Description
quality of life assessment
Time Frame
12 months
Title
DNA methylation analysis of TRPV1 gene
Description
epigenetics modification
Time Frame
12 months
Title
DNA methylation analysis of LY96 gene
Description
epigenetics modificaiton
Time Frame
12 months
Title
DNA methylation analysis of IFNGR1 gene
Description
epigenetics modifications
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult patients age greater than 18 years old end-stage renal failure on two- or three-times per week high-flux HD for more than 90 days mean spKt/Vurea >1.2 per session (for 3 dialysis sessions per week) or spKt/Vurea >1.8 per session (for 2 dialysis sessions per week) Exclusion Criteria: active malignancy unable to give informed consent or complete questionnaires unstable clinical condition defined as significant clinical event requiring hospitalization in the past 90 days unreliable vascular access unable to achieve HD blood flow >150ml/min
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maggie Ming Yee Mok, MBBS, MRCP
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of Nephrology, Department of Medicine, Queen Mary Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Tung Wah Hospital
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No

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Theranova vs High-flux HD Comparison

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