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
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03246984 -
VALUE- Vascular Access Laminate eUropean Experience. A Post Market Surveillance Study to Assess the Safety and Effectiveness of VasQ
|
N/A | |
Completed |
NCT02922361 -
Spending and Outcomes for Complex Medicare Advantage Patients
|
||
Completed |
NCT02235571 -
iChoose Decision Kidney Aid for End-Stage Renal Disease Patients
|
N/A | |
Completed |
NCT01930396 -
Use of Tinzaparin for Anticoagulation in Hemodialysis
|
Phase 4 | |
Completed |
NCT01933789 -
Improving Communication About Serious Illness
|
N/A | |
Completed |
NCT01922843 -
A Phase 2 Study of an Oral Vitamin D Compound (DP001) in Secondary Hyperparathyroidism in Patients on Hemodialysis
|
Phase 2 | |
Not yet recruiting |
NCT01674660 -
Factors Associated With Interdialytic Blood Pressure Variability in Maintenance Hemodialysis Patients
|
N/A | |
Completed |
NCT01209403 -
Insulin-like Growth Factor (IGF-I) in Hemodialysis Patients
|
Phase 4 | |
Not yet recruiting |
NCT01157260 -
The Effects of AST-120 on Endothelial Dysfunction in Patients With Chronic Kidney Disease
|
Phase 4 | |
Completed |
NCT00753116 -
Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertension
|
Phase 1 | |
Recruiting |
NCT00532688 -
N-Acetylcysteine in Heart Failure With Coexistent Chronic Renal Failure
|
Phase 2/Phase 3 | |
Completed |
NCT00528788 -
How Vitamin D Analogues Affect Endothelial Cells in Patients on Dialysis
|
Phase 4 | |
Completed |
NCT00534144 -
Comparison Between Effects of Two Iron Preparations on Protein in the Urine
|
Phase 1 | |
Completed |
NCT00226902 -
Vascular Reactivity in Kidney Disease Patients
|
N/A | |
Completed |
NCT00382044 -
Audit of the Effect of Changing From IV to SC Administration of ESA's in Haemodialysis Patients
|
N/A | |
Recruiting |
NCT00235287 -
Pulse Wave Velocity, Pulse Wave Morphology and Blocking of the Reninangiotensin System in Patients With Chronic Kidney Disease
|
Phase 4 | |
Completed |
NCT00224081 -
DRIVE Trial (Dialysis Patients' Response to Intravenous [IV] Iron With Elevated Ferritin)
|
Phase 4 | |
Completed |
NCT00071214 -
Study to Evaluate the Effectiveness of StaphVAX in Adults on Hemodialysis
|
Phase 3 | |
Completed |
NCT00049907 -
Cardiac and Renal Disease Study (CARDS)
|
N/A | |
Completed |
NCT00006297 -
Risk Factors for CV Disease in a Dialysis Cohort
|
N/A |