Effects of Hemodialysis Plus Hemoperfusion in Maintenance Hemodialysis Patients: A Clinical Study

NCT ID: NCT05639010

Last Updated: 2025-09-29

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 410 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-01-01
• Study Completion Date: 2025-12-31

Brief Summary

This multi-center, open-label, randomized, parallel controlled trial aims to investigate the efficacy of hemoperfusion (HP) in combination with hemodialysis (HD) by assessing blood β2-microglobulin (β2-MG), parathyroid hormone (PTH) and C reactive protein (CRP) clearance in maintenance hemodialysis patients.

Detailed Description

In this HD/HP vs HD trial, the investigators plan to enroll 410 maintenance hemodialysis patients. Twelve medical centers in the Shanghai metropolitan area have expressed interest in participating. Participants will be randomized into 2 groups after a 1-month washout period. The control group (205 patients) will be treated with hemodialysis or hemofiltration with a frequency of 3 times/week; the experimental group (205 patients) will be treated with Jafron KHA80 hemoperfusion apparatus in addition to hemodialysis or hemofiltration with a frequency of 1 time/week. Follow-up data before the last dialysis at 4, 12, 24, 36 and 52 weeks of treatment were collected from both groups, including the following: routine physical examination, laboratory tests (blood routine, blood biochemistry, β2-MG, PTH, CRP, liver/kidney function, coagulation system tests, etc.), chest X-ray, electrocardiogram and cardiac ultrasound. Dialysis adequacy as defined by standard Kt/V will be calculated. Comorbidities, combined medications and adverse events will also be captured. The primary outcomes will include change in blood β2-MG, PTH and CRP values. Secondary outcomes will include change values for serum protein-bound toxins (e.g., p-Cresol sulfate, indophenol sulphate), improvement in patient quality of life (Kidney Disease Quality of Life Short Form), sleep disturbance (Pittsburgh Sleep Quality Index) and pruritus (Duo's pruritus score).

Conditions

End Stage Renal Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

regular hemodialysis

Routine blood purification therapy (including hemodialysis, hemofiltration) 3 times a week

Group Type: ACTIVE_COMPARATOR

regular hemodialysis

Intervention Type: DEVICE

Routine blood purification therapy (including hemodialysis, hemofiltration) 3 times a week

hemoperfusion combined with hemodialysis

Routine blood purification therapy 3 times a week + Combination of hemodialysis and hemoperfusion treatment once a week

Group Type: EXPERIMENTAL

regular hemodialysis

Intervention Type: DEVICE

Routine blood purification therapy (including hemodialysis, hemofiltration) 3 times a week

hemoperfusion combined with hemodialysis

Intervention Type: DEVICE

Hemoperfusion combined with hemodialysis treatment will perform once a week. The hemoperfusion apparatus will use type KHA80 hemoperfusion apparatus (Zhuhai Jafron Biomedical Co., Ltd, China)

Interventions

regular hemodialysis

Routine blood purification therapy (including hemodialysis, hemofiltration) 3 times a week

Intervention Type: DEVICE

hemoperfusion combined with hemodialysis

Hemoperfusion combined with hemodialysis treatment will perform once a week. The hemoperfusion apparatus will use type KHA80 hemoperfusion apparatus (Zhuhai Jafron Biomedical Co., Ltd, China)

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age 18-80 years, regardless of gender

2. Stable maintenance hemodialysis for ≥ 3 months with relatively fixed dialysis pattern

3. Hemodialysis treatment 3 times per week, total treatment duration ≥ 10 hours per week, vascular access unlimited

4. Blood β2-MG > 30 mg/L and/or 300 pg/ml < immunoreactive parathyroid hormone (iPTH) < 800 pg/ml and/or CRP ≥ 16.2 pg/ml

5. Kt/V ≥ 1.2 eight weeks prior to enrollment

6. Signed informed consent form

Exclusion Criteria

1. Known allergic reaction, contraindication or intolerance to the material of the dialyzer or perfusion apparatus

2. Test indicators meeting one or more of the following: white blood cell <4 x 10^9/L, platelet count <60 x 10^9/L, serum albumin <30 g/L

3. Blood flow <200 ml/min

4. Regular hemoperfusion treatment for more than 3 months and at least once every 2 weeks

5. Active bleeding or chronic gastrointestinal bleeding, or other severe bleeding tendencies or coagulation disorders

6. History of unstable angina pectoris, myocardial infarction, severe arrhythmia, pericarditis, myocarditis, cardiac surgery or peripheral vascular surgery in the last 8 weeks

7. Cerebral hemorrhage in the last 12 weeks

8. Severe heart failure (New York Heart Association class IV)

9. Acute infection, acute or critical illnesses such as severe cardiac, pulmonary, hepatic or neurological disease and malignancy

10. Pregnancy or breastfeeding

11. Participation in a clinical trial or ongoing clinical trial within 3 months

12. Expected survival of less than 1 year

13. Not considered suitable for participation in this trial by the investigator

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Changhai Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Zhiyong Guo, professor

Role: STUDY_DIRECTOR

Changhai Hospital

Locations

Changhai Hospital

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Zhiyong Guo, professor

Role: CONTACT

drguozhiyong@163.com

18368328998

Facility Contacts

Zhiyong Guo, professor

Role: primary

drguozhiyong@163.com

18368328998

Other Identifiers

CHEC2022-207

Identifier Type: -

Identifier Source: org_study_id