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Prospective cohort study of membranous nephropathy

Prospective cohort study of membranous nephropathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094033
Enrollment
Unknown
Registered
2024-12-16
Start date
2024-10-22
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

membranous nephropathy

Interventions

Grouping according to different treatment plans:None

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Primary MN confirmed by renal biopsy; 18-80 years old; 2.eGFR > 30ml/min/1.73m2; 3.fully understood this study and voluntarily signed the informed consent;

Exclusion criteria

Exclusion criteria: 1.Secondary MN, such as systemic autoimmune diseases, solid tumors or hematological malignancies, infections, or long-term ingestion of drugs (e.g., gold salts, NSAID, penicillamine); 2.Concomitant with other glomerular diseases, such as diabetic nephropathy, renal significance monoclonal immunoglobulin syndrome (MGRS), small vasculitis renal damage, anti-glomerular basement membrane nephritis, IgA nephropathy, micropathological nephropathy, focal segmental glomerulosclerosis, etc; 3.Malignant tumors (other than local basal cell carcinoma of the skin or cervical cancer in situ) within 5 years, regardless of treatment and with or without signs of local recurrence or metastasis; 4.Hepatitis B surface antigen (HBsAg) or HBV-DNA exceeds the normal range; Hepatitis C virus (HCV) antibody positive; Human immunodeficiency virus (HIV) seropositive; 5.Participate in other clinical trials currently or within the last month; 6.Severe other poorly controlled diseases, including cardiovascular and cerebrovascular diseases requiring hospitalization, cirrhosis, etc., with a life expectancy of < 1 year; 7.Compliance with the study protocol was considered difficult by the treating physician;

Design outcomes

Primary

MeasureTime frame
Urinary protein;serum creatinine;serum albumin;

Secondary

MeasureTime frame
Serum anti- PLA2R antibody;

Countries

China

Contacts

Public ContactMinghui Zhao

Peking University First Hospital

mhzhao@bjmu.edu.cn+86 10 83572388

Outcome results

None listed

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