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A randomized controlled study on the effect of different blood purification modes on the elimination of protein-bound uraemic toxin in dialysis patients

A randomized controlled study on the effect of different blood purification modes on the elimination of protein-bound uraemic toxin in dialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085603
Enrollment
Unknown
Registered
2024-06-13
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

hemodialysis

Interventions

Experimental Group 1:HD 3 times/2 weeks, HDF 1 time/2 weeks, HD+pHA130 1 time/week
Experimental Group 2:HD 5 times/2 weeks, HD+pHA130 1 time/2 weeks
control group:HD 5 times/2 weeks, HDF 1 time/2 weeks

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients with end-stage renal disease undergoing maintenance hemodialysis treatment; (2) Age between 18 and 75 years old, no gender limitation; (3) Regular hemodialysis, 3 times per week, 4 hours per session, treatment duration = 3 months; (4) Using autologous arteriovenous fistula or transplanted intravascular fistula as vascular acces and have a blood flow = 200ml/min. (5) Willing and able to receive treatment according to the requirements of the program, and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients treated with a combination of hemodialysis and peritoneal dialysis; (2) Patients who have undergone hemoperfusion therapy for more than one month in the past three months. (3) Patients who are known to have allergic reactions, contraindications, or intolerance to dialyzer materials; (4) Patients with acute severe infection, severe cardiopulmonary insufficiency, severe cerebrovascular disease, severe bleeding tendency or active bleeding, malignant tumors, etc.; (5) Patients with a platelet count less than 60×109/L; (6) Patients with a life expectancy of less than 2 years; (7) Patients currently or recently (within 30 days) participating in other clinical trials; (8) Patients who refuse to sign the informed consent form; (9) Other situations where researchers deem it inappropriate to participate in this study

Design outcomes

Primary

MeasureTime frame
Clearance rate of protein-bound toxin of indoxyl sulfate (IS);

Secondary

MeasureTime frame
Clearance rate of YKL-40;Clearance rate of PCS;Decline rate of ß2-microglobulin;hemodialysis-related complications;routine blood test;blood chemistry;serum lipid parameter;blood pressure;quality of life;Pruritus;Pittsburgh sleep quality index,PSQI;

Countries

China

Contacts

Public ContactShaobin Yu

West China Hospital, Sichuan University

407577669@qq.com+86 159 2854 2141

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026