此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Adequacy of Haemodiafiltration: Middle Molecules Clearance, Patients Reported Outcomes and Sodium Balance

2026年7月16日 更新者:East and North Hertfordshire NHS Trust
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.

研究概览

详细说明

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.

研究类型

观察性的

注册 (估计的)

300

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Usama Afzal Butt, MBBS, MRCP (UK)
  • 电话号码:+441438284340
  • 邮箱:usama.butt1@nhs.net

学习地点

    • Hertfordshire
      • Stevenage、Hertfordshire、英国、SG1 4AB
        • 招聘中
        • Lister Hospital, East and North Hertfordshire NHS Trust
        • 接触:
        • 首席研究员:
          • Enric Vilar, MBChB, MRCP, PhD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

Adult patients with ESKD receiving hemodialysis accross 5 dialysis units in East and North Hertfordshire NHS Trust , UK.

描述

Inclusion Criteria:

  • 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)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
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

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Effect of high (≥23L) versus low volume HDF (<23L) on middle molecules clearance and on clinical and patients reported outcomes.
大体时间: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.

12 months
Effect of dialysis fluid sodium concentration of (137 vs 140 mmol/L) on overhydration volume in patients on HD and HDF.
大体时间: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.
12 months

次要结果测量

结果测量
措施说明
大体时间
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.
大体时间:5 years
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.
5 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Usama Afzal Butt, MBBS, MRCP、East and North Hertfordshire NHS Trust

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年1月9日

初级完成 (估计的)

2030年11月1日

研究完成 (估计的)

2030年11月1日

研究注册日期

首次提交

2026年7月2日

首先提交符合 QC 标准的

2026年7月16日

首次发布 (实际的)

2026年7月21日

研究记录更新

最后更新发布 (实际的)

2026年7月21日

上次提交的符合 QC 标准的更新

2026年7月16日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅