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A prospective clinical observational study protocol for patients with membranous nephropathy

A prospective clinical observational study protocol for patients with membranous nephropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103206
Enrollment
Unknown
Registered
2025-05-27
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Membranous nephropathy

Interventions

Supportive treatment group:None
Glucocorticoid + cyclophosphamide group:None
Glucocorticoid + calcineurin inhibitor (CNI) group:None
The rituximab group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with membranous nephropathy (MN) diagnosed by renal biopsy in the Department of Nephrology, West China Hospital, Sichuan University from October 1, 2024 were enrolled. 2. Over 18 years old, no gender, race, etc.; 3. Patients with regular follow-up, i.e., at least every 3 months for 1 year after diagnosis until completion of 1 year of follow-up (prospective cohort). Demographic, clinical, and laboratory data will be collected at baseline, and relevant laboratory data will be collected every 3-6 months thereafter until study completion.

Exclusion criteria

Exclusion criteria: 1. Patients with membranous nephropathy due to secondary causes, including: known infection with hepatitis B or C virus or HIV; known malignant disease; positive double-stranded DNA antibody; currently treated with penicillamine, non-steroidal anti-inflammatory drugs, cytotoxic drugs or cyclosporine; treated with corticosteroids for more than 3 months in the previous two years; pregnant or contraceptive; or previous adverse reactions to prednisolone, methylprednisolone, chlorambucil or cyclosporine; 2. Patients who cannot be followed regularly.

Design outcomes

Primary

MeasureTime frame
Creatinine;Urine protein creatinine ratio;24-hour urinary protein quantity;The eGFR;Urinalysis;

Secondary

MeasureTime frame
Urea;Uric Acid;ENA antibody profile;Blood routine examination;Complement factor 3;Complement factor 4;PLA2R;

Countries

China

Contacts

Public ContactQin Wei

West China Hospital of Sichuan University

qinweihx@scu.edu.cn+86 189 8060 2119

Outcome results

None listed

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