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A multicenter prospective cohort study of membranous nephropathy patients based on systems biology informatics

A multicenter prospective cohort study of membranous nephropathy patients based on systems biology informatics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101140
Enrollment
Unknown
Registered
2025-04-21
Start date
2024-05-12
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Membranous Nephropathy

Interventions

Complete remission:None
Partial remission:None
Ineffective group:None

Sponsors

Wuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age range: 18-80 years (including both 18 and 80), gender, and ethnicity are not restricted. 2.Patients diagnosed with primary membranous nephropathy (PMN) according to the KDIGO 2021 diagnostic criteria, regardless of whether they have received immunosuppressive treatment. 3.Individuals with the capacity for autonomous decision-making who can independently decide whether to participate in this study.

Exclusion criteria

Exclusion criteria: 1.Onset of nephrotic syndrome in infants and children. 2.Secondary membranous nephropathy (e.g., associated with systemic autoimmune diseases, solid or hematologic malignancies, chronic hepatitis B virus infection, and other infections) or prolonged use of certain medications (e.g., gold salts, nonsteroidal anti-inflammatory drugs [NSAIDs], penicillamine). 3.History of malignant tumors. 4.Currently undergoing kidney dialysis or expected to require dialysis during the study. 5.Abnormal liver function, with alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels exceeding three times the upper limit of normal. 6.Inability to cooperate with researchers in basic information collection due to various reasons (e.g., hearing impairment, language barriers). 7.Other reasons that the researcher deems unsuitable for participation in the study (e.g., low willingness to cooperate, difficulties in long-term follow-up).

Design outcomes

Primary

MeasureTime frame
24-hour urine protein quantification;Anti-phospholipase A2 receptor antibody IgG;Anti-phospholipase A2 receptor antibody domain- IgG/IgG4 antibodies;Serum creatinine;Serum Albumin;Urine Protein-to-Creatinine Ratio ;Urine Protein;Estimated glomerular filtration rate;

Secondary

MeasureTime frame
Anti-Phospholipase A2 Receptor Antibody Gene Polymorphism;Alanine Aminotransferase;Aspartate Aminotransferase;Fasting Blood Glucose;Serum Potassium;Total Cholesterol;Triglycerides;Cluster of Differentiation 20 Count;Tacrolimus concentration;Hemoglobin;Platelet count;Microscopic hematuria;Human Leukocyte Antigen gene polymorphism;

Countries

China

Contacts

Public ContactWang Liang

Wuxi People's Hospital

wangliang@medmail.com.cn+86 137 7101 9880

Outcome results

None listed

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