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SASH: Sodium Accumulation Study In Haemodialysis

Sodium Accumulation Study In Haemodialysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05128188
Acronym
SASH
Enrollment
10
Registered
2021-11-19
Start date
2022-03-01
Completion date
2023-09-02
Last updated
2024-08-09

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

Conditions

End Stage Renal Disease on Dialysis, Haemodialysis

Brief summary

Haemodialysis (HD) sustains life in patients with end-stage kidney disease (ESKD) but is associated with a marked increase in incidence of cardiovascular disease (CVD) and high annual mortality rates. The pathogenesis of CVD in patients on HD is multifactorial and complex but hypertension is thought to be a major contributing factor. Sodium balance is normally regulated by the kidneys in health but has to be achieved by sodium removal during HD for those with ESKD. Recent evidence suggests that accumulation of sodium in the skin and / or muscle may be a critical factor impacting the development of hypertension and CVD in patients with ESKD and non-invasive methods are therefore required to study tissue sodium accumulation in this context. This study aims to determine the change in skin and muscle sodium content in patients undergoing haemodialysis. Participants will have a single haemodialysis session, and undergo two MRI scans (one prior to and one following dialysis).

Detailed description

It has been proposed that tissue sodium accumulation in skin and/or muscle is a key factor in hypertension. 23Na MRI allows the assessment of skin and muscle sodium storage and will therefore be a valuable tool in elucidating the role of tissue sodium accumulation in the pathogenesis of salt-sensitive hypertension and cardiovascular morbidity and mortality. Moreover, if haemodialysis in patients with end-stage kidney disease (ESKD) results in changes in tissue sodium, the development of 23Na skin and muscle measures would allow for a method to correlate skin tissue sodium content with detailed cardiovascular and functional assessments. Participants will have a single haemodialysis session, and undergo two MRI scans (one prior to and one following dialysis), in conjunction with clinical data collection (eg. blood samples, bioimpedance analysis, skin autoflorescence).

Interventions

OTHERNo intervention will be given in this study

No intervention will be given in this study

Sponsors

University Hospitals of Derby and Burton NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
50 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 50-75 years inclusive * Male patients with CKD stage 5 receiving chronic haemodialysis * Patient has been dialysis dependent for at least 3 months * Must be able to follow simple instruction in English (on safety ground for MRI scans) and be able to understand the nature and requirements of the study

Exclusion criteria

* Active infection or malignancy * Amputee * Pregnancy * Contraindication to MRI scanning including claustrophobia, pacemaker, metallic implants etc * Unable or unwilling to provide informed consent * Medical conditions or overall physical frailty precludes scan session in opinion of investigator * Any condition which could interfere with the patient's ability to comply with the study

Design outcomes

Primary

MeasureTime frameDescription
Ascertainment of MRI measures of muscle sodium content in 100% of patients studied6 monthsSodium imaging of the skin and muscle of the upper calf will be performed using a range of sequences to quantify sodium in the skin and muscle using both fast-field-echo (FFE) and ultrashort TE (UTE) imaging techniques.
Ascertainment of MRI measures of skin sodium content in 100% of patients studied6 monthsSodium imaging of the skin and muscle of the upper calf will be performed using a range of sequences to quantify sodium in the skin and muscle using both fast-field-echo (FFE) and ultrashort TE (UTE) imaging techniques.

Secondary

MeasureTime frameDescription
To study skin sodium in haemodialysis patients and compare with previously reported healthy normal values6 monthsSodium imaging of the skin and muscle of the upper calf will be performed using a range of sequences to quantify sodium in the skin and muscle using both fast-field-echo (FFE) and ultrashort TE (UTE) imaging techniques
To study muscle sodium in haemodialysis patients and compare with previously reported healthy normal values6 monthsSodium imaging of the skin and muscle of the upper calf will be performed using a range of sequences to quantify sodium in the skin and muscle using both fast-field-echo (FFE) and ultrashort TE (UTE) imaging techniques
To measure degree of change in skin sodium content in relation to a single haemodialysis treatment6 monthsQuantification of sodium in skin and muscle and compare finding before and after dialysis
To measure degree of change in muscle sodium content in relation to a single haemodialysis treatment6 monthsQuantification of sodium in skin and muscle and compare finding before and after dialysis

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026