Kidney Failure, Chronic Clinical Trial
Official title:
Short-Term Effects of the FX-Class of Haemodialyser on Quality of Life and Inflammatory Markers in Stable Dialysis Patients
Background:
The new hollow fibre FX-class of dialysers (Fresenius Medical Care, Bad Homburg, Germany)
features a number of technological improvements that may benefit the patient. This includes
the use of the advanced high-flux polysulfone membrane, Helixone®, which has an extremely
high endotoxin retaining capability. Theoretically leading to reduced systemic inflammation
in the patient, which is an important factor for morbidity and mortality with dialysis.
The dialysis membrane is the first to be manufactured using membrane-spinning procedures
(nano-controlled spinning technology) that enables the membrane to be modulated at the
nano-scale level. The resultant membrane is able to extremely efficiently remove middle
molecules, along with minimal loss of albumin.
These features may lead to improved patient outcomes, including reduced systemic
inflammation and improved quality of life.
Aims:
1. To assess the short-term effects of the FX-class Dialyser on quality of life in stable
haemodialysis patients
2. To assess the short-term effects of the FX-class Dialyser on inflammatory markers in
stable haemodialysis patients.
Methods Patient selection All patients in the Joondalup Health Campus satellite dialysis
unit will be invited to participate in this study.
Inclusion criteria –
1. Age >18years
2. Able to provide informed consent
3. On haemodialysis for 3 months
Exclusion criteria –
1. Active inflammatory, infective or neoplastic process within the last 1 month
2. Active major psychiatric condition
3. Currently on haemodiafiltration as haemodialysis modality
Design This study will involve an unblinded, cross-over design, with patients being
randomised upon entry into one of 2 groups. The 2 groups will be - 1. HF80 dialyser (this is
the best of the currently used dialysers and therefore no participant will require a
reduction in their dialysis during this trial); and 2. FX dialyser. Patients will have
baseline tests performed prior to intervention and then repeated after 3 months. At 3
months, patients will then cross-over into the other group and tests repeated after a
further 6 months.
Due to the nature of the intervention, blinding will not be practical. The cross-over design
will allow maximum power for this fixed and relatively small dialysis population (~50
patients).
Independent variables –
1. Dialysis prescription on enrolment
a. Including dialyser type (biocompatibility)
2. Adequacy of dialysis
1. Urea reduction ratio
2. Kt/V
3. Anaemia
1. Including iron studies
2. Including erythropoietin usage
4. Calcium phosphate balance
a. Including Parathyroid hormone levels
5. Serum albumin
Outcome markers –
1. Quality of Life (i) KD-QOL – this is a standardised quality of life questionnaire
designed and validated for dialysis patients, that will be readily comparable to other
studies.
(ii) Feeling thermometer
2. Inflammatory markers (i) High sensitivity c-reactive protein (ii) IL-6 (iii) White cell
count.
Statistical analysis:
Quality of life measures and inflammatory markers will be analysed using paired t-test after
normality demonstrated. Simple and multiple linear regression analysis will then be
performed to examine associations between independent variables with changes in the outcome
variables. STATA 8.2 will be used to assist with the analysis
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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