- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07679763
Randomized Cross-Over Comparison of Medium Cut-Off and High-Flux Hemodialysis Membranes (MCO-HD)
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.
Přehled studie
Postavení
Detailní popis
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.
Typ studie
Zápis (Odhadovaný)
Fáze
- Nelze použít
Kontakty a umístění
Studijní kontakt
- Jméno: Veysel Baran Tomar, M.D.
- Telefonní číslo: +905334133253
- E-mail: veyselbarantomar@gazi.edu.tr
Studijní místa
-
-
Ankara
-
Ankara, Ankara, Turecko (Türkiye), 06500
- Gazi University Faculty of Medicine, Department of Nephrology, Hemodialysis Unit
-
Kontakt:
- Veysel Baran Tomar, M.D.
- Telefonní číslo: +905334133253
- E-mail: veyselbarantomar@gazi.edu.tr
-
Kontakt:
- Omer Faruk Akcay, Associate Professor
- Telefonní číslo: +905546992867
- E-mail: omerfarukakcay@gazi.edu.tr
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Crossover Assignment
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: 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).
|
|
Experimentální: 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).
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Change in Serum Interleukin-6 (IL-6)
Časové okno: 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)
Časové okno: 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)
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Change in Pulse Wave Velocity (PWV)
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Publikace a užitečné odkazy
Obecné publikace
- Zickler D, Schindler R, Willy K, Martus P, Pawlak M, Storr M, Hulko M, Boehler T, Glomb MA, Liehr K, Henning C, Templin M, Trojanowicz B, Ulrich C, Werner K, Fiedler R, Girndt M. Medium Cut-Off (MCO) Membranes Reduce Inflammation in Chronic Dialysis Patients-A Randomized Controlled Clinical Trial. PLoS One. 2017 Jan 13;12(1):e0169024. doi: 10.1371/journal.pone.0169024. eCollection 2017.
- Yang J, Ke G, Liao Y, Guo Y, Gao X. Efficacy of medium cut-off dialyzers and comparison with high-flux dialyzers in patients on maintenance hemodialysis: A systematic review and meta-analysis. Ther Apher Dial. 2022 Aug;26(4):756-768. doi: 10.1111/1744-9987.13755. Epub 2021 Dec 4.
- Kirsch AH, Lyko R, Nilsson LG, Beck W, Amdahl M, Lechner P, Schneider A, Wanner C, Rosenkranz AR, Krieter DH. Performance of hemodialysis with novel medium cut-off dialyzers. Nephrol Dial Transplant. 2017 Jan 1;32(1):165-172. doi: 10.1093/ndt/gfw310.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Urogenitální onemocnění
- Patologické procesy
- Mužská urogenitální onemocnění
- Onemocnění ledvin
- Urologická onemocnění
- Ženské urogenitální onemocnění
- Ženské urogenitální onemocnění a těhotenské komplikace
- Chronické onemocnění
- Atributy nemoci
- Renální insuficience
- Renální insuficience, chronická
- Patologické stavy, příznaky a symptomy
- Kardiovaskulární choroby
- Zánět
- Selhání ledvin, chronické
Další identifikační čísla studie
- GAZI-HD-MCO-HF-2026
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Popis plánu IPD
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na Medium Cut-Off Hemodialysis Membrane
-
Charite University, Berlin, GermanyDokončenoCévní kalcifikaceNěmecko
-
Manchester University NHS Foundation TrustBaxter Healthcare Corporation; Manchester Metropolitan UniversityDokončenoKardiovaskulární choroby | Zánět | Konečné stadium onemocnění ledvinSpojené království
-
Vantive Health LLCBaxter Healthcare CorporationDokončenoKonečné stadium onemocnění ledvinŠpanělsko
-
Carlo Maria GuastoniNeznámý
-
Sisli Hamidiye Etfal Training and Research HospitalDokončenoRenální insuficience, chronická | Selhání ledvin | Komplikace související s dialýzouKrocan
-
Marc RighiniUniversity Hospital, Angers; University Hospital, Brest; Academisch Medisch Centrum...DokončenoPlicní embolieŠvýcarsko, Francie, Holandsko
-
Hacettepe UniversityNeznámýBolesti v kříži | Zůstatek; Zkreslený
-
Gangnam Severance HospitalDokončenoChronické onemocnění ledvin vyžadující chronickou dialýzuKorejská republika
-
Fundación SenefroNeznámýChronické onemocnění ledvin vyžadující chronickou dialýzuŠpanělsko
-
Vantive Health LLCBaxter Healthcare CorporationDokončenoAkutní selhání ledvin | Chronické selhání ledvinČína