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Recruiting NCT06561191

NCT06561191 Functionality of Albumin in the Context of Hemodialysis

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Clinical Trial Summary
NCT ID NCT06561191
Status Recruiting
Phase
Sponsor Universität Duisburg-Essen
Condition Albumin
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2024-08-01
Primary Completion 2025-12

Trial Parameters

Condition Albumin
Sponsor Universität Duisburg-Essen
Study Type INTERVENTIONAL
Phase N/A
Enrollment 50
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-08-01
Completion 2025-12
Interventions
Hemodialysis mode, dialyzer type

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Brief Summary

Hemodialysis treatment enables patients with end-stage chronic kidney disease to survive. At the same time, however, this treatment also increases cardiovascular mortality, in particular due to a chronically increased level of inflammation and usually incomplete removal of uraemic toxins. Both of these are closely linked with the functional properties of albumin. The aim of this study is to investigate the effects of various parameters of dialysis, in particular dialyzer properties and dialysis mode on the functional properties of albumin and to what extent these parameters can be used therapeutically, to improve the treatment quality of hemodialysis treatment in the long term by modifying albumin functional properties. Our own preliminary work in this field and the current state of research indicate that, for example, the use of high-flux dialyzers can contribute to a reduction of the oxidative stress level. It also appears possible that treatment mode (haemodiafiltration instead of haemodialysis) may also have an effect on the binding and detoxification efficiency of albumin and thus on the removal of uraemic toxins. Previous results have mostly been collected in observational studies. As a proof-of-concept study, this study will further investigate the concrete therapeutic applicability in an interventional study design.

Eligibility Criteria

Inclusion Criteria: * 18 years or older at least 3 month of hemodialysis treatment (3x/week) with constant dialysis treatment regimen Exclusion Criteria: * Age ≤ 18 years * Less than three months of regular (3x/week) hemodialysis treatments or less than 3 treatments/week * Acute or chronic liver disease (Child stage A or higher or fulfillment of the of the Kings College criteria) * Infusion of commercial human albumin (e.g. in the context of ascites drainage) in the last three months prior to study inclusion * Acute or severe chronic infections * Acute tumor disease

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