HaemodiafiltrationNCT07717255
Adequacy of Haemodiafiltration: Middle Molecules Clearance, Patients Reported Outcomes and Sodium Balance
An observational study of Haemodiafiltration and Haemodialysis, run by East and North Hertfordshire NHS Trust at 1 site in United Kingdom.
Trial summary
The goal of this observational study is to understand the differences in terms of middle molecules clearance and patient outcomes in High (>23Litres (L)) vs Low (<23 L) convection volume (CV) Hemodiafiltration (HDF) and to understand the effect of dialysate fluid sodium concentration (137 vs 140 mmol/L) on… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Haemodiafiltration, Haemodialysis, Patient Reported Outcome Measurements
- How many people
- 300 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 9 Jan 2025to 1 Nov 2030
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adult patients with ESKD receiving hemodialysis accross 5 dialysis units in East and North Hertfordshire NHS Trust , UK.
Who may be able to join
- Age 18 years or above.
- Ability to give informed consent.
- End stage kidney disease (ESKD) treated by haemodialysis for at least 3 months.
- Prognosis > 6 months as assessed by principal investigator (PI)
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United Kingdom1 site, 1 recruiting
- Recruiting
Lister Hospital, East and North Hertfordshire NHS Trust
Stevenage, Hertfordshire, SG1 4AB
Usama Afzal Butt, MBBS, MRCP, +441438284340, usama.butt1@nhs.net
Enric Vilar, MBChB, MRCP, PhD
About this study
The goal of this observational study is to understand the differences in terms of middle molecules clearance and patient outcomes in High (>23Litres (L)) vs Low (<23 L) convection volume (CV) Hemodiafiltration (HDF) and to understand the effect of dialysate fluid sodium concentration (137 vs 140 mmol/L) on overhydration volume in patients on HD and HDF.
Read the detailed description
Background and Rationale The concept of normalised urea clearance (Kt/V) to determine the efficiency of dialysis emerged over four decades ago. This is based on evidence that Kt/V below a certain threshold is associated with poor outcomes , although the survival benefit appears to be capped beyond a threshold of around 1.2 . Dialysis techniques have evolved significantly since this evidence emerged. Routine use of high-flux membranes and convective treatments/Haemodiafiltration (HDF), increase removal of toxins of larger molecular weight such as middle molecules. Some of these have direct toxic potential unlike urea. Nevertheless, the metric of dialysis efficiency is still based on conventional small molecule clearance which doesn't correlate with removal of more clinically relevant middle molecules removed during HDF. Moreover, the relationship of small molecules clearance with patient reported symptoms and their nutritional status remains inconsistent. Most recent dialysis prescription guidelines highlight the limitations of Kt/V and suggest using this parameter as only one aspect of dialysis efficiency amongst others including nutrition, bone and mineral metabolism, salt and fluid homeostasis and anaemia management. Updating measure of dialysis quality to align more with current dialysis practice (HDF) seems a logical step. There are multiple aspects of quality of dialysis including toxins clearance, dialysis related symptoms burden, quality of life, fluid status and nutrition. This study aims to develop a metric of HDF adequacy which encompass these aspects comprehensively.
1.1 Toxins clearance and dialysis symptoms burden
One of the recent advances in dialysis is increasing use of haemodiafiltration (HDF) which appears to improve survival when large convection volumes are delivered. There is no agreed definition for high-volume HDF but it is generally accepted that ≥23 liters convection volume per session is high volume HDF since this volume has been associated with a beneficial survival outcome in most recent HDF trial (CONVINCE Trial). It is unclear though, what drives the benefit of high volume HDF. Convective treatment removes more middle molecules (such as β2-Microglobulin (β2M)) compared to conventional diffusive treatments, and enhanced middle molecules clearance is considered a plausible mechanism of survival benefit . Direct evidence for this though, is lacking. In the absence of an instrument to measure dialysis efficiency in HDF, currently the HDF prescription relies on achieving the same small molecule clearance as conventional HD and additionally achieving a certain convection volume. Interestingly by achieving the desirable convection volume, the delivered small molecules clearance exceeds the threshold at which survival benefit was reported to be capped in HEMO study. This method of HDF prescription needs to be rationalised. Measuring middle molecules clearance - as β2M clearance - could reflect the convection volume as well as small molecules clearance. Such a strategy may have a role in assessment of HDF adequacy. However, given the strong correlation between serum β2M and RKF, the impacts of RKF on β2M clearance need to be taken into consideration before using this tool to assess the HDF adequacy. This study intends to explore the relationship between HDF convection volume and β2M clearance and the change in this relationship with declining kidney function.
Whilst survival is considered the outcome of primary importance in clinical trials, there are other outcomes which may be of similar or greater importance to patients and carers. The Standardised outcomes in Nephrology (SONG) is a global initiative to establish set of core outcomes for research across the spectrum of kidney disease. These outcomes are developed based on the shared priorities of all relevant stakeholders. While high volume HDF has been shown to be related to better survival, there is little data on the relationship between HDF convection volume and important patient reported outcomes such a Fatigue, Recovery time after dialysis and cognitive function. It is important to understand the impact of HDF volume or its potential surrogate middle molecules clearance on these important outcomes. Similarly, it is unclear if HDF volume or Middle molecules clearance is related to other important aspects of dialysis efficiency such as bone and mineral metabolism, cumulative phosphate binder use and nutritional status. Many of these patient reported outcomes and biochemical and nutritional markers are important components of SONG-HD outcomes. Understanding these relationships could lead to development of more comprehensive and clinically relevant dialysis efficiency marker in HDF.
1.2 Dialysate sodium and fluid status
Sodium and fluid handling are the fundamental aspects of dialysis in end stage kidney disease (ESKD). There is wealth of evidence to relate fluid and sodium dysregulation with poor outcomes in dialysis patients. Despite this the optimal dialysate sodium concentration remains controversial. Different dialysis units use different standard dialysate sodium concentration. Fluid and sodium handling could potentially be more important in HDF compared to HD due to exposure to large convection volume and sodium retention due to Gibbs-Donnan effect in HDF. In-fact one plausible mechanism of benefit in HDF is better haemodynamic stability possibly as a result of fluid and salt retention. Although there is no evidence of bioimpedance measured fluid retention in high volume HDF compared to HD, the fluid status in HDF has not been assessed with varying dialysate sodium and with varying delivered convection volume. Optimum dialysate sodium or Dialysate - plasma sodium gradient in HDF remains an important but uncertain aspect of HDF prescription. This study aims to explore the effect of different dialysate sodium levels on patients' volume status in HD and HDF and also with varying HDF convection volume.
- Conditions
- Haemodiafiltration, Haemodialysis, Patient Reported Outcome Measurements, Nutrition, Malnutrition (Calorie), Fluid Balance Outcomes
- Keywords
- Middle molecules clearance in haemodiafiltraion, Effect of dialysis clearance on nutritional status, Effect of dialysis clearance on patient reported outcome measure, Effect of dialysate sodium on fluid status
- Medical subject headings
- Malnutrition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| HDF group | Particiapants receiving hemodiafiltration | |
| HD group | Participants receiving high flux hemodialysis | |
| Low dialysate sodium group | Participants dialysing with dialysate sodium concentration 137 mmol/L | |
| High dialysate sodium group | Participants dialysing with dialysate sodium concentration 137 mmol/L |
What is being measured
The primary outcome is the main question the study is designed to answer.
Effect of high (≥23L) versus low volume HDF (<23L) on middle molecules clearance and on clinical and patients reported outcomes.
- Effect of high (≥23L) versus low volume HDF (<23L) on β2M clearance.
- Effect of high (≥23L) versus low volume HDF (<23L) on dialysis related symptom score (measured using IPOS-Renal questionnaire).
- Effect of high (≥23L) versus low volume HDF (<23L) on cognitive function (Assessed using PROMIS cognitive function short form).
- Effect of high (≥23L) versus low volume HDF (<23L) on malnutrition score (Measured using modified subjective global assessment tool).
- Effect of high (≥23L) versus low volume HDF (<23L) on serum phosphate level (mmol/L).
- Effect of high (≥23L) versus low volume HDF (<23L) on phosphate binder dose (mg/day).
This will be measured cross-sectionally at 0,6 and 12 month time points and longitudinally over time correcting for variables including residual renal function.
Measured: 12 months
Effect of dialysis fluid sodium concentration of (137 vs 140 mmol/L) on overhydration volume in patients on HD and HDF.
Effect of dialysis fluid sodium concentration of (137 vs 140 mmol/L) on overhydration volume (measured with Bioimpedance) in patients on HD and HDF. This will be assessed cross-sectionally at 0,6 and 12 months and also longitudinally over time correcting for confounding variables such as RKF.
Measured: 12 months
Secondary outcomes (1)
Correlation between middle molecule clearance (β2M clearance) with rate of major adverse cardiovascular events (non-fatal MI, Non-fatal stroke, cardiovascular death) and all cause hospitalizations.
Correlation between middle molecule clearance (β2M clearance) with rate of major adverse cardiovascular events (non-fatal MI, Non-fatal stroke, cardiovascular death) and all cause hospitalizations.
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jul 2026
- Study start9 Jan 2025
- Primary completion1 Nov 2030 (estimated)
- Study completion1 Nov 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HaemodiafiltrationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 300 participants (estimated)
Sponsor and investigators
- Lead sponsor
- East and North Hertfordshire NHS Trust
- Sponsor type
- Other government
- Responsible party
- Sponsor
- Investigators
- Usama Afzal Butt, MBBS, MRCP, Principal investigator, East and North Hertfordshire NHS Trust
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07717255
- Sponsor's protocol ID
- RD2024-52
- Other IDs
- IRAS, REC
- Status last verified
- Jul 2026
- First submitted
- 2 Jul 2026
- Last updated
- 21 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 21 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Adequacy of Haemodiafiltration: Middle Molecules Clearance, Patients Reported Outcomes and Sodium Balance
- ClinicalTrials.gov ID
- NCT07717255
- Acronym / sponsor ID
- RD2024-52
- Conditions
- Haemodiafiltration, Haemodialysis, Patient Reported Outcome Measurements, Nutrition, Malnutrition (Calorie), Fluid Balance Outcomes
- Keywords
- Middle molecules clearance in haemodiafiltraion, Effect of dialysis clearance on nutritional status, Effect of dialysis clearance on patient reported outcome measure, Effect of dialysate sodium on fluid status
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- East and North Hertfordshire NHS TrustOther government
- Study start
- 9 Jan 2025 (actual)
- Primary completion
- 1 Nov 2030 (estimated)
- Study completion
- 1 Nov 2030 (estimated)
- First posted
- 21 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational study is to understand the differences in terms of middle molecules clearance and patient outcomes in High (>23Litres (L)) vs Low (<23 L) convection volume (CV) Hemodiafiltration (HDF) and to understand the effect of dialysate fluid sodium concentration (137 vs 140 mmol/L) on overhydration volume in patients on HD and HDF.
Detailed description
Background and Rationale The concept of normalised urea clearance (Kt/V) to determine the efficiency of dialysis emerged over four decades ago. This is based on evidence that Kt/V below a certain threshold is associated with poor outcomes , although the survival benefit appears to be capped beyond a threshold of around 1.2 . Dialysis techniques have evolved significantly since this evidence emerged. Routine use of high-flux membranes and convective treatments/Haemodiafiltration (HDF), increase removal of toxins of larger molecular weight such as middle molecules. Some of these have direct toxic potential unlike urea. Nevertheless, the metric of dialysis efficiency is still based on conventional small molecule clearance which doesn't correlate with removal of more clinically relevant middle molecules removed during HDF. Moreover, the relationship of small molecules clearance with patient reported symptoms and their nutritional status remains inconsistent. Most recent dialysis prescription guidelines highlight the limitations of Kt/V and suggest using this parameter as only one aspect of dialysis efficiency amongst others including nutrition, bone and mineral metabolism, salt and fluid homeostasis and anaemia management. Updating measure of dialysis quality to align more with current dialysis practice (HDF) seems a logical step. There are multiple aspects of quality of dialysis including toxins clearance, dialysis related symptoms burden, quality of life, fluid status and nutrition. This study aims to develop a metric of HDF adequacy which encompass these aspects comprehensively.
1.1 Toxins clearance and dialysis symptoms burden
One of the recent advances in dialysis is increasing use of haemodiafiltration (HDF) which appears to improve survival when large convection volumes are delivered. There is no agreed definition for high-volume HDF but it is generally accepted that ≥23 liters convection volume per session is high volume HDF since this volume has been associated with a beneficial survival outcome in most recent HDF trial (CONVINCE Trial). It is unclear though, what drives the benefit of high volume HDF. Convective treatment removes more middle molecules (such as β2-Microglobulin (β2M)) compared to conventional diffusive treatments, and enhanced middle molecules clearance is considered a plausible mechanism of survival benefit . Direct evidence for this though, is lacking. In the absence of an instrument to measure dialysis efficiency in HDF, currently the HDF prescription relies on achieving the same small molecule clearance as conventional HD and additionally achieving a certain convection volume. Interestingly by achieving the desirable convection volume, the delivered small molecules clearance exceeds the threshold at which survival benefit was reported to be capped in HEMO study. This method of HDF prescription needs to be rationalised. Measuring middle molecules clearance - as β2M clearance - could reflect the convection volume as well as small molecules clearance. Such a strategy may have a role in assessment of HDF adequacy. However, given the strong correlation between serum β2M and RKF, the impacts of RKF on β2M clearance need to be taken into consideration before using this tool to assess the HDF adequacy. This study intends to explore the relationship between HDF convection volume and β2M clearance and the change in this relationship with declining kidney function.
Whilst survival is considered the outcome of primary importance in clinical trials, there are other outcomes which may be of similar or greater importance to patients and carers. The Standardised outcomes in Nephrology (SONG) is a global initiative to establish set of core outcomes for research across the spectrum of kidney disease. These outcomes are developed based on the shared priorities of all relevant stakeholders. While high volume HDF has been shown to be related to better survival, there is little data on the relationship between HDF convection volume and important patient reported outcomes such a Fatigue, Recovery time after dialysis and cognitive function. It is important to understand the impact of HDF volume or its potential surrogate middle molecules clearance on these important outcomes. Similarly, it is unclear if HDF volume or Middle molecules clearance is related to other important aspects of dialysis efficiency such as bone and mineral metabolism, cumulative phosphate binder use and nutritional status. Many of these patient reported outcomes and biochemical and nutritional markers are important components of SONG-HD outcomes. Understanding these relationships could lead to development of more comprehensive and clinically relevant dialysis efficiency marker in HDF.
1.2 Dialysate sodium and fluid status
Sodium and fluid handling are the fundamental aspects of dialysis in end stage kidney disease (ESKD). There is wealth of evidence to relate fluid and sodium dysregulation with poor outcomes in dialysis patients. Despite this the optimal dialysate sodium concentration remains controversial. Different dialysis units use different standard dialysate sodium concentration. Fluid and sodium handling could potentially be more important in HDF compared to HD due to exposure to large convection volume and sodium retention due to Gibbs-Donnan effect in HDF. In-fact one plausible mechanism of benefit in HDF is better haemodynamic stability possibly as a result of fluid and salt retention. Although there is no evidence of bioimpedance measured fluid retention in high volume HDF compared to HD, the fluid status in HDF has not been assessed with varying dialysate sodium and with varying delivered convection volume. Optimum dialysate sodium or Dialysate - plasma sodium gradient in HDF remains an important but uncertain aspect of HDF prescription. This study aims to explore the effect of different dialysate sodium levels on patients' volume status in HD and HDF and also with varying HDF convection volume.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| HDF group | – | –Particiapants receiving hemodiafiltration |
| HD group | – | –Participants receiving high flux hemodialysis |
| Low dialysate sodium group | – | –Participants dialysing with dialysate sodium concentration 137 mmol/L |
| High dialysate sodium group | – | –Participants dialysing with dialysate sodium concentration 137 mmol/L |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients with ESKD receiving hemodialysis accross 5 dialysis units in East and North Hertfordshire NHS Trust , UK.
Key inclusion criteria (4 listed)
- Age 18 years or above.
- Ability to give informed consent.
- End stage kidney disease (ESKD) treated by haemodialysis for at least 3 months.
- Prognosis > 6 months as assessed by principal investigator (PI)
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Effect of high (≥23L) versus low volume HDF (<23L) on middle molecules clearance and on clinical and patients reported outcomes.
Time frame: 12 months
1. Effect of high (≥23L) versus low volume HDF (<23L) on β2M clearance. 2. Effect of high (≥23L) versus low volume HDF (<23L) on dialysis related symptom score (measured using IPOS-Renal questionnaire). 3. Effect of high (≥23L) versus low volume HDF (<23L) on cognitive function (Assessed using PROMIS cognitive function short form). 4. Effect of high (≥23L) versus low volume HDF (<23L) on malnutrition score (Measured using modified subjective global assessment tool). 5. Effect of high (≥23L) versus low volume HDF (<23L) on serum phosphate level (mmol/L). 6. Effect of high (≥23L) versus low volume HDF (<23L) on phosphate binder dose (mg/day). This will be measured cross-sectionally at 0,6 and 12 month time points and longitudinally over time correcting for variables including residual renal function.
Effect of dialysis fluid sodium concentration of (137 vs 140 mmol/L) on overhydration volume in patients on HD and HDF.
Time frame: 12 months
Effect of dialysis fluid sodium concentration of (137 vs 140 mmol/L) on overhydration volume (measured with Bioimpedance) in patients on HD and HDF. This will be assessed cross-sectionally at 0,6 and 12 months and also longitudinally over time correcting for confounding variables such as RKF.
1 secondary outcome
Correlation between middle molecule clearance (β2M clearance) with rate of major adverse cardiovascular events (non-fatal MI, Non-fatal stroke, cardiovascular death) and all cause hospitalizations.
Time frame: 5 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Jul 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Usama Afzal Butt, MBBS, MRCP principal investigator
East and North Hertfordshire NHS Trust
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Haemodiafiltration and Haemodialysis, run by East and North Hertfordshire NHS Trust at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 21 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Usama Afzal Butt, MBBS, MRCP (UK) (+441438284340, usama.butt1@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Effect of high (≥23L) versus low volume HDF (<23L) on middle molecules clearance and on clinical and patients reported outcomes. (time frame: 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2026.