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Prospective clinical observational study of patients with minimal change nephropathy/focal segmental glomerulosclerosis

Prospective clinical observational study of patients with minimal change nephropathy/focal segmental glomerulosclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104136
Enrollment
Unknown
Registered
2025-06-11
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Minimal change nephropathy/focal segmental glomerulosclerosis

Interventions

rituximab group:None

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who were diagnosed with MCD/FSGS (MN) by renal biopsy in the outpatient/inpatient department of nephrology of West China Hospital of Sichuan University from May 1, 2025 were included; 2. Patients over 18 years old, regardless of gender or race; 3. Patients with regular follow-up.

Exclusion criteria

Exclusion criteria: 1.Patients with MCD/FSGS caused by secondary causes; 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 and methylprednisolone; 2. patients who cannot be followed up regularly.

Design outcomes

Primary

MeasureTime frame
creatinine;Estimate glomerular filtration rate;urea;Uric Acid;urinalysis;Urine protein-creatinine ratio;

Secondary

MeasureTime frame
.Blood routine examination;ANA and antinuclear antibody profile;Complement C3;Complement C4;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