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The application of Protein A Immunoadsorption Technology in Autoantibody-Mediated Rapidly Progressive Glomerulonephritis

The application of Protein A Immunoadsorption Technology in Autoantibody-Mediated Rapidly Progressive Glomerulonephritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095886
Enrollment
Unknown
Registered
2025-01-15
Start date
2023-05-08
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Rapidly Progressive Glomerulonephritis

Interventions

Control Group:sing conventional drug immunosuppressive therapy (glucocorticoids +/- immunosuppressants), and not using extracorporeal blood purification treatment to clear pathogenic antibodies (inclu
Intervention Group:On the basis of conventional drug treatment, protein A immunoadsorption therapy is used.

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 70 years old; 2. No gender restrictions; 3. Positive for serum anti-glomerular basement membrane antibodies (GBM+) or positive for anti-neutrophil cytoplasmic antibodies (ANCA+); 4. Clinical diagnosis of rapidly progressive nephritis; 5. The patient or legal representative agrees and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant women; 2. Individuals with consciousness disturbances who are unable to communicate; 3. Individuals with psychiatric disorders who are non-compliant with treatment; 4. Patients currently receiving angiotensin-converting enzyme inhibitor (ACEI) therapy and cannot discontinue it; 5. Patients with relative contraindications to extracorporeal circulation therapy (such as shock, hypercoagulable state, severe bleeding or bleeding tendency, etc.); 6. Individuals with a history of intolerance to plasma exchange and allergies to other extracorporeal circulation therapies; 7. Individuals with multiple organ dysfunction; 8. Other situations deemed unsuitable for participation in the study by the investigator.

Design outcomes

Primary

MeasureTime frame
The change in titer of autoantibodies (GBM or ANCA);

Secondary

MeasureTime frame
the change of IgG;The rate of renal function recovery;

Countries

China

Contacts

Public ContactYingying Yang

Department of Nephrology, West China Hospital, Sichuan University

yingyingyangsf@163.com+86 136 8839 8045

Outcome results

None listed

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