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A pilot study on the elimination of uremic toxin by hemoperfusion in maintenance hemodialysis patients

A pilot study on the elimination of uremic toxin by hemoperfusion in maintenance hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102415
Enrollment
Unknown
Registered
2025-05-14
Start date
2024-10-10
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Chronic kidney disease Stage 5

Interventions

Experimental group:Hemoperfusion
Control group:None

Sponsors

Renji Hospital affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.18-75 years old, regardless of gender; 2.Maintenance hemodialysis (>=3 months) and blood purification treatment 3 times a week; 3.The vascular access was autologous arteriovenous fistula or artificial vessels, and the blood flow was =200mL/min; 4.spKT/V>=1.2; 5.Voluntarily sign informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients who have participated in other clinical studies within 1 month; 2.Pregnant or lactating women; 3.Patients with a New York College of Cardiology (NYHA) grade 4 or who had acute coronary syndrome or myocardial infarction within 3 months prior to study start; 4.Patients with active bleeding within 2 weeks (such as cerebral hemorrhage, digestive tract hemorrhage, fundus hemorrhage, etc.); 5.Patients with low blood pressure (pre-dialysis blood pressure =140g/L); 6.Patients with severe infections (hypersensitive C-reactive protein levels 10 times higher than the upper limit of normal); 7.Platelet count < 60×109/L or white blood cell count < 4×109/ L; 8.Patients with a history of drug addiction or serious mental disorders; 9.Other investigators considered that they could not participate in the study;

Design outcomes

Primary

MeasureTime frame
? free light chain;Tumor necrosis factor-a;Fibroblast growth factor23;Interleukin-6;YKL-40;

Secondary

MeasureTime frame
P-Cresol;YKL-40;Tumor necrosis factor-a;Interleukin-6;Fibroblast growth factor23;Indoxyl sulfate;? free light chain;

Countries

China

Contacts

Public ContactRenhua Lu

Renji Hospital affiliated to Shanghai Jiaotong University School of Medicine

lurenhua1977@hotmail.com+86 21 58752345

Outcome results

None listed

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