Skip to content

Short Term Effects of FX Dialysers on QOL and Inflammation

Short-Term Effects of the FX-Class of Haemodialyser on Quality of Life and Inflammatory Markers in Stable Dialysis Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00291603
Enrollment
50
Registered
2006-02-14
Start date
2006-02-28
Completion date
2006-12-31
Last updated
2007-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Failure, Chronic

Keywords

dialysis, Renal Dialysis, inflammation, quality of life, End Stage Kidney Failure

Brief summary

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.

Detailed description

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

Interventions

DEVICEFX-class of dialyser

Sponsors

Sir Charles Gairdner Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 outcomes

Primary

MeasureTime frame
KD-QOL
Feeling Thermometer

Secondary

MeasureTime frame
IL-6
TNF-alpha
hs-CRP
white cell count

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026