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Randomized Cross-Over Comparison of Medium Cut-Off and High-Flux Hemodialysis Membranes (MCO-HD)

8 september 2026 bijgewerkt door: Veysel Baran TOMAR, Gazi University

Randomized Cross-Over Evaluation of Medium Cut-Off and High-Flux Hemodialysis Membranes on Inflammation and Cardiovascular Function in Maintenance Hemodialysis Patients

Patients receiving maintenance hemodialysis are at increased risk of cardiovascular disease, chronic inflammation, endothelial dysfunction, and impaired quality of life. Medium cut-Off (MCO) hemodialysis membranes have been developed to enhance the removal of middle-molecular-weight uremic toxins compared with conventional high-flux membranes, which may improve inflammatory status and cardiovascular health.

The aim of this study is to compare the effects of MCO and high-flux hemodialysis membranes on inflammatory biomarkers and cardiovascular function in adult patients receiving maintenance hemodialysis. The primary outcomes are changes in serum interleukin-6 (IL-6) and vascular cell adhesion molecule-1 (VCAM-1) levels. Secondary outcomes include arterial stiffness assessed by pulse wave velocity (PWV), body composition assessed by Body Composition Monitor (BCM), handgrip strength, and patient-reported outcomes including quality of life, pruritus, and pain scores.

This is a prospective, randomized, open-label, two-sequence, two-period crossover study conducted at Gazi University Faculty of Medicine. Thirty adult hemodialysis patients will be randomized to one of two treatment sequences. Participants in Sequence A will receive MCO dialysis membranes for the first 3 months followed by high-flux membranes for the next 3 months. Participants in Sequence B will receive high-flux membranes for the first 3 months followed by MCO membranes for the next 3 months. Blood samples and clinical assessments will be performed at baseline, month 3, and month 6.

The study is expected to provide evidence regarding the effects of different dialysis membrane technologies on inflammation and cardiovascular health and may contribute to optimizing membrane selection in routine hemodialysis practice.

Studie Overzicht

Gedetailleerde beschrijving

Cardiovascular disease remains the leading cause of morbidity and mortality in patients receiving maintenance hemodialysis. Chronic inflammation, endothelial dysfunction, vascular stiffness, and the accumulation of middle-molecular-weight uremic toxins are considered important contributors to adverse cardiovascular outcomes in this population. Conventional high-flux hemodialysis membranes provide effective small-solute clearance but have limited capacity for removing larger middle molecules involved in inflammation and vascular injury.

Medium cut-off (MCO) membranes have been developed to enhance the clearance of larger middle molecules while maintaining albumin retention within acceptable limits. Previous studies have suggested that MCO membranes may improve inflammatory profiles and patient-centered outcomes; however, data regarding their effects on endothelial dysfunction, arterial stiffness, body composition, and patient-reported outcomes remain limited.

This study is designed as a prospective, randomized, open-label, two-sequence, two-period crossover clinical investigation comparing MCO and high-flux hemodialysis membranes in maintenance hemodialysis patients. Participants will be randomized in a 1:1 ratio to one of two treatment sequences. Sequence A will receive MCO membranes during Period 1 (Months 0-3) followed by high-flux membranes during Period 2 (Months 3-6). Sequence B will receive high-flux membranes during Period 1 followed by MCO membranes during Period 2. This crossover design allows each participant to serve as his or her own control, thereby reducing inter-individual variability.

Study assessments will be performed at baseline, Month 3, and Month 6. In addition to routine laboratory testing performed during standard hemodialysis follow-up, blood samples will be obtained at baseline, Month 3, and Month 6 for the measurement of serum interleukin-6 (IL-6) and vascular cell adhesion molecule-1 (VCAM-1). Cardiovascular assessment will include pulse wave velocity (PWV) measurement. Nutritional and body composition status will be evaluated using Body Composition Monitor (BCM) parameters, including overhydration, ECW/TBW ratio, intracellular water, lean tissue index, body cell mass, and phase angle. Functional status will be assessed by handgrip strength measurement. Patient-reported outcomes will be evaluated using the Kidney Disease Quality of Life-36 (KDQOL-36), UP-Dial pruritus questionnaire, and Short-Form McGill Pain Questionnaire (SF-MPQ).

The primary objective is to compare the effects of MCO and high-flux membranes on IL-6 and VCAM-1 levels. Secondary objectives include evaluation of arterial stiffness, body composition, physical function, and patient-reported outcomes. The findings may provide clinically relevant evidence regarding membrane selection strategies in routine hemodialysis practice.

Studietype

Ingrijpend

Inschrijving (Geschat)

30

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Ankara
      • Ankara, Ankara, Turkije (Türkiye), 06500
        • Gazi University Faculty of Medicine, Department of Nephrology, Hemodialysis Unit

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Age 18 to 80 years.
  • Receiving maintenance hemodialysis for at least 6 months.
  • Clinically stable and receiving thrice-weekly hemodialysis.
  • Able to comply with study procedures, questionnaires, and scheduled assessments.
  • Able and willing to provide written informed consent.

Exclusion Criteria:

  • Acute infection at screening or enrollment.
  • Major surgery within the previous 3 months.
  • Active malignancy requiring ongoing treatment.
  • Terminal illness with limited life expectancy.
  • Physical or cognitive impairment preventing completion of study procedures or questionnaires.
  • Inability or unwillingness to provide written informed consent.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Sequence A (MCO to High-Flux)
Participants randomized to Sequence A will receive medium cut-off (MCO) hemodialysis membranes during Period 1 (Months 0-3), followed by high-flux hemodialysis membranes during Period 2 (Months 3-6). Hemodialysis will be performed three times weekly according to standard clinical practice. Clinical, laboratory, and patient-reported outcome assessments will be performed at baseline, Month 3, and Month 6.
Medium cut-off (MCO) hemodialysis membrane used as part of routine maintenance hemodialysis treatment. MCO membranes are designed to enhance the clearance of larger middle-molecular-weight uremic toxins while maintaining clinically acceptable albumin retention. Participants assigned to MCO treatment periods will receive thrice-weekly hemodialysis according to standard clinical practice. In this study, MCO treatment will be delivered using the ELISIO™ MCO series (Nipro).
High-flux hemodialysis membrane used as part of routine maintenance hemodialysis treatment. High-flux membranes represent the current standard dialysis technology and provide effective clearance of small solutes and selected middle molecules. Participants assigned to high-flux treatment periods will receive thrice-weekly hemodialysis according to standard clinical practice. In this study, high-flux treatment will be delivered using the ELISIO™ HF series (Nipro).
Experimenteel: Sequence B (High-Flux to MCO)
Participants randomized to Sequence B will receive high-flux hemodialysis membranes during Period 1 (Months 0-3), followed by medium cut-off (MCO) hemodialysis membranes during Period 2 (Months 3-6). Hemodialysis will be performed three times weekly according to standard clinical practice. Clinical, laboratory, and patient-reported outcome assessments will be performed at baseline, Month 3, and Month 6.
Medium cut-off (MCO) hemodialysis membrane used as part of routine maintenance hemodialysis treatment. MCO membranes are designed to enhance the clearance of larger middle-molecular-weight uremic toxins while maintaining clinically acceptable albumin retention. Participants assigned to MCO treatment periods will receive thrice-weekly hemodialysis according to standard clinical practice. In this study, MCO treatment will be delivered using the ELISIO™ MCO series (Nipro).
High-flux hemodialysis membrane used as part of routine maintenance hemodialysis treatment. High-flux membranes represent the current standard dialysis technology and provide effective clearance of small solutes and selected middle molecules. Participants assigned to high-flux treatment periods will receive thrice-weekly hemodialysis according to standard clinical practice. In this study, high-flux treatment will be delivered using the ELISIO™ HF series (Nipro).

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Serum Interleukin-6 (IL-6)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Comparison of serum interleukin-6 (IL-6) concentrations during treatment with medium cut-off and high-flux hemodialysis membranes.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Serum Vascular Cell Adhesion Molecule-1 (VCAM-1)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Comparison of serum vascular cell adhesion molecule-1 (VCAM-1) concentrations during treatment with medium cut-off and high-flux hemodialysis membranes.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Pulse Wave Velocity (PWV)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of arterial stiffness by pulse wave velocity measurements.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Handgrip Strength
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of physical function using handgrip strength measurement.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Kidney Disease Quality of Life-36 (KDQOL-36) Score
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Evaluation of patient-reported quality of life using the KDQOL-36 questionnaire.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in UP-Dial Pruritus Score
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Evaluation of pruritus severity using the Uraemic Pruritus in Dialysis Patients (UP-Dial) scale. The UP-Dial total score ranges from 0 to 56, with higher scores indicating more severe pruritus and a worse outcome.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Short-Form McGill Pain Questionnaire (SF-MPQ) Score
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Evaluation of pain using the Short-Form McGill Pain Questionnaire (SF-MPQ) total Pain Rating Index score. The SF-MPQ total Pain Rating Index score is calculated from 15 pain descriptors, each scored from 0 to 3, resulting in a total score range of 0 to 45. Higher scores indicate greater pain severity and a worse outcome.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Overhydration (OH)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of overhydration (OH, L) measured using the Body Composition Monitor (BCM).
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Extracellular Water to Total Body Water Ratio (ECW/TBW)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of the extracellular water to total body water ratio (ECW/TBW) using the Body Composition Monitor (BCM).
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Intracellular Water (ICW)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of intracellular water (ICW, L) using the Body Composition Monitor (BCM).
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Lean Tissue Index (LTI)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of lean tissue index (LTI, kg/m²) using the Body Composition Monitor (BCM).
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Change in Body Cell Mass (BCM)
Tijdsspanne: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)
Assessment of body cell mass (BCM, kg) using the Body Composition Monitor.
At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 juli 2026

Primaire voltooiing (Geschat)

1 januari 2027

Studie voltooiing (Geschat)

1 januari 2027

Studieregistratiedata

Eerst ingediend

24 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

30 juni 2026

Eerst geplaatst (Werkelijk)

1 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

9 september 2026

Laatste update ingediend die voldeed aan QC-criteria

8 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual participant data (IPD) are not planned to be shared publicly. The study involves a limited number of participants from a single center, and data will be retained and managed in accordance with institutional policies, ethical requirements, and applicable data protection regulations.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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