Randomised Study of High-flux Haemodialysis and Haemodiafiltration
- Conditions
- End Stage Renal Disease
- Interventions
- Other: High-flux haemodialysisProcedure: Haemodiafiltration
- Registration Number
- NCT01862679
- Lead Sponsor
- NHS Greater Glasgow and Clyde
- Brief Summary
The most common forms of renal replacement therapy currently in use are high flux haemodialysis (HF-HD) and haemodiafiltration (HDF). Although these techniques appear similar to the patient, there are important differences in what happens to the blood as it travels through the dialysis machine.
During HDF, the machine controls hydrostatic pressure across the dialyser to remove additional water together with toxins from the blood and this fluid volume is continually replaced with an ultra-pure solution. HDF has a theoretical advantage removing more waste substances, especially larger molecules, from the blood than HF-HD which may be of benefit to the patient in the medium to long term.Despite the theoretical advantages, trials have so far been unable to find any significant difference in death rates or the development of health problems among patients on HDF or HF-HD.
It is therefore important to examine other factors which may help doctors and patients to decide which treatment to use. The investigators have designed a study which aims to answer three main questions:
1. Does HDF make patients feel better?
2. Is blood pressure more stable on HDF in comparison with HF-HD?
3. Are Phosphate levels and other blood parameters better controlled with HDF than HF-HD?
The investigators will do this by randomly assigning patients on HF-HD to receive 2 months of either HF-HD or HDF with as equivalent treatment prescriptions as possible and without the patient knowing which treatment they are receiving. After two months the patients will switch to the alternative form of dialysis for a further two months. During the study the investigators will ask the patients how long it took them to recover from the preceding session of dialysis, assess the frequency of symptomatic low blood pressure and also perform blood tests at set intervals to measure specific blood parameters.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- Receiving HF-HD for at least 3 months
- Reliable vascular access (i.e. use of the same fistula, graft or tunnelled central venous catheter for at least 1 month)
- Aged 18 or older
- Currently receiving HDF
- Emergency hospital admissions within the preceding 4 weeks
- Life expectancy less than 6 months
- Neoplasia
- Unable to give informed consent
- Unable to perform QoL questionnaire or self report recovery post-dialysis time
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description 8 weeks HF haemodialysis / 8 weeks HD-filtration High-flux haemodialysis 8 weeks high-flux haemodialysis followed by 8 weeks haemodiafiltration 8 weeks HD-filtration /8 weeks HF haemodialysis High-flux haemodialysis 8 weeks haemodiafiltration followed by 8 weeks high-flux haemodialysis 8 weeks HF haemodialysis / 8 weeks HD-filtration Haemodiafiltration 8 weeks high-flux haemodialysis followed by 8 weeks haemodiafiltration 8 weeks HD-filtration /8 weeks HF haemodialysis Haemodiafiltration 8 weeks haemodiafiltration followed by 8 weeks high-flux haemodialysis
- Primary Outcome Measures
Name Time Method Change in the average time taken to fully recover post dialysis Baseline compared 8 week treatment point Self-assessment by patient of hours/mins to full recovery after dialysis
- Secondary Outcome Measures
Name Time Method Number of symptomatic hypotension events Number of events noted by nurse at each dialysis session in each of the two arms of the study. Each arm= 3 sessions per week for 8 weeks Number of dialysis circuit clotting events Number of events noted by nurse at each dialysis session in each of the two arms of the study. Each arm= 3 sessions per week for 8 weeks Pre-dialysis serum concentrations of beta-2-microglobulin Measured at baseline, and after 4 and 8 weeks of each treatment period Pre-dialysis serum concentrations of potassium Measured at baseline, and after 4 and 8 weeks of each treatment period Pre-dialysis serum concentrations of betaine Measured at baseline, and after 4 and 8 weeks of each treatment period Pre-dialysis serum concentrations of interleukin-6 Measured at baseline, and after 4 and 8 weeks of each treatment period Pre-dialysis serum concentrations of phosphate Measured at baseline, and after 4 and 8 weeks of each treatment period Kt/V urea. : Measured at baseline, and after 4 and 8 weeks of each treatment period Pre-dialysis serum concentrations of vitamin B12. Measured at baseline, and after 4 and 8 weeks of each treatment period Pre-dialysis serum concentrations of PTH. Measured at baseline, and after 4 and 8 weeks of each treatment period
Trial Locations
- Locations (1)
NHS Greater Glasgow andClyde
🇬🇧Glasgow, United Kingdom