High-flux dialyzer
Devicea dialyzer meeting the definition of high-flux
NCT Number: NCT04106310
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:
1. Removal of small molecules (e.g. urea), middle molecules (Beta-2 microglobulin, Phosphate and Creatinine) and protein bound solutes 2. Markers of inflammation, ossification and fibrosis 3. 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.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Division of Nephrology, Department of Medicine, Queen Mary Hospital, Hong Kong
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)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
a dialyzer meeting the definition of high-flux
a middle cut-off dialyzer
Time frame: 12 months
measured by Body Composition Monitor
Time frame: 12 months
measured by weight (in kilograms) divided by the square of heights (in meters)
Time frame: 12 months
endogenous inhibitor of nitric oxide synthase, one of the cardiovascular biomarkers
Time frame: 12 months
biomarker for bone turnover
Time frame: 12 months
biomarker for atherosclerosis and bone turnover
Time frame: 12 months
measurement of clearance of urea by hemodialysis therapy, a marker for adequacy of dialysis
Time frame: 12 months
middle size uremic toxin
Time frame: 12 months
middle to large molecular size uremic toxin
Time frame: 12 months
a marker for endothelial dysfunction
Time frame: 12 months
a marker for endothelial dysfunction
Time frame: 12 months
indication of anemia
Time frame: 12 months
marker for inflammation
Time frame: 12 months
marker for inflammation
Time frame: 12 months
marker for inflammation
Time frame: 12 months
marker for nutritional status
Time frame: 12 months
marker for nutritional status and appetite
Time frame: 12 months
nutritional marker
Time frame: 12 months
small size uremic waste produce
Time frame: 12 months
reflects lipid control
Time frame: 12 months
reflects lipid control
Time frame: 12 months
reflects lipid control
Time frame: 12 months
a measurement scale reflecting nutritional status
Time frame: 12 months
a measurement scale reflecting nutritional status
Time frame: 12 months
nutritional marker measured by Body Composition Monitor
Time frame: 12 months
number of admisisons due to cardiovascular events during the follow-up period
Time frame: 12 months
number of admissions due to infection during the follow-up period
Time frame: 12 months
number of deaths during the follow-up period
Time frame: 12 months
Symptomatology scale to measure itchiness
Time frame: 12 months
Symptomatology scale to measure itchiness
Time frame: 12 months
measurement scale for appetite
Time frame: 12 months
measurement scale for appetite
Time frame: 12 months
number of time required to feel well after receiving a hemodialysis session
Time frame: 12 months
scale to rate the quality of sleep
Time frame: 12 months
measurement of cognitive function
Time frame: 12 months
quality of life assessment
Time frame: 12 months
epigenetics modification
Time frame: 12 months
epigenetics modificaiton
Time frame: 12 months
epigenetics modifications
The University of Hong Kong
Other
The Comparison of Expanded Dialysis With Theranova Dialyzer With Conventional High-flux Hemodialysis
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