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Does Incremental Initiation of Haemodialysis Preserve Native Kidney Function?

Does Incremental Initiation of Haemodialysis Preserve Native Kidney Function? A Multicentre Feasibility Randomised Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03418181
Acronym
IncrementalHD
Enrollment
44
Registered
2018-02-01
Start date
2018-01-08
Completion date
2020-05-31
Last updated
2026-07-15

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

Conditions

Dialysis, Kidney Failure

Keywords

Residual Kidney Function, Haemodialysis, Preserve Residual Kidney Function

Brief summary

Patients who start haemodialysis usually retain some natural kidney function for months or years after starting dialysis. Even a small amount of this natural kidney function can be helpful in reducing the need for dietary and fluid restriction. There is also good evidence that retaining a small amount of natural kidney function may provide a survival benefit for patients on dialysis. Most patients who commence haemodialysis start three times per week for 3.5-4 hours per session, irrespective of the amount of natural kidney function they may have. An alternative approach used in some kidney units is to take account of the natural kidney function in prescribing the amount of dialysis. This may allow patients to start treatment needing to spend less time on dialysis or even to start just twice weekly. The amount of dialysis can be adjusted over time as natural kidney function declines. This is called "incremental haemodialysis". Both of these approaches are considered to be standard care although it is not known which approach is more beneficial to patients. There are some suggestions that the frequency of dialysis may influence the rate of decline of natural kidney function but this need to be tested in a large randomised study. To inform the design of such a study, a smaller scale feasibility study is required. We intend to randomise fifty new starters on haemodialysis with adequate natural kidney function into two groups - a group who will have dialysis prescribed in the standard fashion - three times weekly for 3.5-4 hours per session or a group who will have an incremental start beginning with twice weekly treatment. We will investigate how many patients have sufficient natural kidney function to be eligible, whether patients are willing to participate and continue in the study, compare the rate of loss of kidney function between groups, and ascertain whether this individualised dialysis approach is less intrusive to patients. The results will be used to design a larger definitive study.

Detailed description

This study is feasibility randomised controlled trial. 54 patients who have newly started on haemodialysis will be recruited into the study from 4 UK centres. Eligible patients will be approached prior to initiation of dialysis or after starting dialysis. The details of the study will be explained to them and a Patient Information sheet will be provided. Interested participants will be invited to the study and a written consent will be obtained. The participants will be randomly allocated to 2 groups. 1. Thrice weekly dialysis (control arm) 2. Incremental dialysis - Twice weekly dialysis to start with and slowly increasing the duration and frequency of dialysis to thrice weekly depending on their native kidney function. All participants will be monitored at least once monthly by performing dialysis related blood tests, urine tests, clinical evaluation, medications, weight, dialysis adequacy, adverse events. Questionnaire involving quality of life, mood, illness intrusiveness, functional status, cognitive function will also be performed. Participants will be recruited in the first year and all participants will be followed up for 12 months. All participants may withdraw at any time without any change in their dialysis care. To ensure independence, the University of Hertfordshire will perform randomisation, and assist with data monitoring and data analysis. A 6 month rate of loss of native kidney function between the 2 groups will be analysed.

Interventions

PROCEDUREStandard Haemodialysis

Thrice weekly dialysis.

PROCEDUREIncremental dialysis

Individualised dialysis dose according to native kidney function.

Sponsors

East and North Hertfordshire NHS Trust
Lead SponsorOTHER_GOV
University of Hertfordshire
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The participants will be randomly allocated to 2 groups: 1. Thrice weekly dialysis (control arm) 2. Incremental dialysis - Twice weekly dialysis to start with and slowly increasing the duration and frequency of dialysis to thrice weekly depending on their native kidney function.

Eligibility

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

Inclusion criteria

* Age ≥ 18 years * Advanced renal failure due to underlying primary kidney disease and established as a new starter on haemodialysis within the previous 3 months * Residual Kidney Function likely to permit twice weekly dialysis as defined by interdialytic urea clearance ≥3ml/min/1.73m2 BSA measured routinely as part of standard care * Sufficient understanding of the study procedures and requirements including capacity for explicit agreement to be randomised to standard or incremental HD regimens

Exclusion criteria

* Planned organ transplantation and already on another interventional trial within 3 months from study screening * Anticipated requirement for high-volume ultrafiltration on dialysis (e.g. subjects with daily enteral or parenteral nutrition) * Blood-borne virus positivity * Subjects unable to comply with requirement for monthly interdialytic urine collection. * Pregnancy * Prognosis \<12 months as judged by PI

Design outcomes

Primary

MeasureTime frameDescription
Recruitability12 monthsNumber of patients potentially eligible for screening during the study period
Recruitability - study criteria met12 monthsProportion of screened patients who fulfil study criteria.
Recruitability - partcipation in the study12 monthsProportion of patients approached who agree to participate in the study.
Retainability12 monthsProportion of patients randomised who withdraw from the study and the reasons for their withdrawal.
Protocol Adherence12 monthsProportion of patients who adhere to protocol dialysis frequency.
Incidence of hospital admissions due to hyperkalemia, fluid overload, lower respiratory tract infection [Safety of the study]12 monthsFrequency of hospital admission due to hyperkalemia and fluid overload, and lower respiratory tract infection (LRTI).
Effect size6 months after randomisationRate of change (mean) of RKF in the first 6 months after randomisation.
Dialysis dose6 months after randomisationDialysis dose measured by eKT/V
Residual kidney function6 months after randomisationResidual kidney function measured by eKT/V

Secondary

MeasureTime frameDescription
Quality of life12 monthsAssessed using EQ-5D-5L questionnaire.
Depression12 monthsAssessed using PHQ-9 questionnaire.
Illness intrusiveness12 monthsAssessed using Illness intrusiveness rating scale.
Changes in cognitive function12 monthsAssessed by MOCA tool.
Functional status12 monthsAssessed by Clinical Frailty Score (CFS).
Incidence of vascular access failures [Safety]12 monthsFrequency of vascular access failures and interventions.
Major Adverse Cardiac Events12 monthsAssessed by recording of the frequency of the events.
Survival12 monthsMeasured by all-cause mortality

Countries

United Kingdom

Contacts

PRINCIPAL_INVESTIGATORDr Enric Vilar

East and North Hertfordshire NHS Trust

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 16, 2026