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NCT Number: NCT07685223

Medium Cut-Off and High-Flux Membranes on Mineral and Bone Metabolism in Hemodialysis Patients

This study aims to compare the effects of medium cut-off (MCO) and high-flux hemodialysis membranes on mineral and bone metabolism biomarkers in patients receiving maintenance hemodialysis. Chronic kidney disease-mineral and bone disorder (CKD-MBD) is characterized by disturbances in biomarkers such as fibroblast growth factor-23 (FGF-23) and sclerostin, which are associated with bone turnover, vascular calcification, and adverse clinical outcomes.

This is a single-center, prospective, randomized, open-label, two-sequence, two-period crossover clinical study. Thirty adult patients receiving maintenance hemodialysis will be randomized to receive either MCO membrane treatment followed by high-flux membrane treatment or the reverse sequence, with each treatment period lasting three months.

Serum FGF-23 and sclerostin levels will be measured at baseline, Month 3, and Month 6. Additional assessments will include pulse wave velocity (PWV), body composition monitoring (BCM), handgrip strength, health-related quality of life (KDQOL-36), pruritus severity (UP-Dial), and pain assessment (SF-MPQ). The study will evaluate whether MCO membranes provide additional benefits compared with conventional high-flux membranes regarding CKD-MBD-related biomarkers and patient-centered outcomes.

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Key information

About this study

Chronic kidney disease-mineral and bone disorder (CKD-MBD) is a common complication in patients receiving maintenance hemodialysis and is associated with abnormalities in mineral metabolism, bone turnover, vascular calcification, and increased cardiovascular risk. Biomarkers such as fibroblast growth factor-23 (FGF-23) and sclerostin play important roles in the pathophysiology of CKD-MBD and have been associated with adverse clinical outcomes in patients with end-stage kidney disease.

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. Because FGF-23 and sclerostin are relatively large circulating molecules, MCO membranes may provide improved clearance and potentially influence CKD-MBD-related biological pathways.

This study is a single-center, prospective, randomized, open-label, two-sequence, two-period crossover clinical investigation conducted in maintenance hemodialysis patients. Eligible participants will be randomized in a 1:1 ratio to one of two treatment sequences. Sequence A will receive MCO hemodialysis for three months followed by high-flux hemodialysis for three months. Sequence B will receive high-flux hemodialysis for three months followed by MCO hemodialysis for three months.

Assessments will be performed at baseline, Month 3, and Month 6. Primary outcome measures include changes in serum FGF-23 and sclerostin concentrations. Secondary outcome measures include changes in pulse wave velocity (PWV), body composition parameters measured by BCM, handgrip strength, health-related quality of life (KDQOL-36), pruritus severity (UP-Dial), and pain characteristics (SF-MPQ).

Routine laboratory evaluations will be performed according to standard clinical practice. In addition, blood samples will be collected for FGF-23 and sclerostin measurements at each study visit. Safety assessments will include monitoring of adverse events, dialysis-related intolerance, and clinically significant medical events throughout the study period.

The results of this study are expected to provide evidence regarding the effects of MCO membranes on CKD-MBD-related biomarkers and patient-centered outcomes and may contribute to optimizing membrane selection strategies in maintenance hemodialysis practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Medium Cut-Off Hemodialysis Membrane

Device

A medium cut-off (MCO) hemodialysis membrane used during maintenance hemodialysis treatment. Participants assigned to MCO treatment will receive thrice-weekly hemodialysis according to standard clinical practice. The intervention is intended to enhance the removal of middle-molecular-weight solutes and to evaluate its effects on mineral and bone metabolism biomarkers, including fibroblast growth factor-23 (FGF-23) and sclerostin, as well as body composition, vascular stiffness, and patient-reported outcomes.

High-Flux Hemodialysis Membrane

Device

A conventional high-flux hemodialysis membrane used during maintenance hemodialysis treatment. Participants assigned to high-flux treatment will receive thrice-weekly hemodialysis according to standard clinical practice. This intervention serves as the comparator for evaluating the effects of medium cut-off membranes on mineral and bone metabolism biomarkers, including fibroblast growth factor-23 (FGF-23) and sclerostin, as well as body composition, vascular stiffness, and patient-reported outcomes.

Primary outcomes

  1. Change in Serum Fibroblast Growth Factor-23 (FGF-23)

    Time frame: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)

    Change in serum fibroblast growth factor-23 (FGF-23) concentrations during treatment with medium cut-off and high-flux hemodialysis membranes. Serum FGF-23 levels will be measured using ELISA and compared between treatment periods.

  2. Change in Serum Sclerostin

    Time frame: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)

    Change in serum sclerostin concentrations during treatment with medium cut-off and high-flux hemodialysis membranes. Serum sclerostin levels will be measured using ELISA and compared between treatment periods.

Secondary outcomes

  1. Change in Pulse Wave Velocity (PWV) Measured in m/s

    Time frame: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)

    Pulse wave velocity (PWV) will be measured in meters per second (m/s) as a single parameter of arterial stiffness. Change in PWV from baseline to Month 3 and Month 6 will be compared between medium cut-off and high-flux hemodialysis membrane treatment periods.

  2. Change in Handgrip Strength Measured by Hand Dynamometer

    Time frame: At baseline (July 2026), Month 3 (October 2026), and Month 6 (January 2027)

    Handgrip strength will be measured in kilograms (kg) using a hand dynamometer. The same prespecified measurement method will be used at each study visit. Change in handgrip strength from baseline to Month 3 and Month 6 will be compared between medium cut-off and high-flux hemodialysis membrane treatment periods.

  3. Change in Kidney Disease Quality of Life-36 (KDQOL-36) Score

    Time frame: 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.

  4. Change in UP-Dial Pruritus Score

    Time frame: 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.

  5. Change in Short-Form McGill Pain Questionnaire (SF-MPQ) Score

    Time frame: 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.

  6. Change in Overhydration (OH)

    Time frame: 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).

  7. Change in Extracellular Water to Total Body Water Ratio (ECW/TBW)

    Time frame: 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).

  8. Change in Intracellular Water (ICW)

    Time frame: 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).

  9. Change in Lean Tissue Index (LTI)

    Time frame: 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).

  10. Change in Body Cell Mass (BCM)

    Time frame: 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Veysel Baran Tomar, M.D.

CONTACT

[email protected]

+905334133253

Sponsors and collaborators

Lead sponsor

Gazi University

Other

Collaborators

  • Nipro Medical Corporation

Registry information

Official study title

Prospective Comparative Evaluation of the Effects of Medium Cut-Off and High-Flux Hemodialysis Membranes on Mineral and Bone Metabolism Biomarkers and Body Composition in Maintenance Hemodialysis Patients

Acronym: MBD-HD

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 6, 2026
Registry last updated
Jul 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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