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A retrospective control study of low concentration of tacrolimus combined with prednisone in the treatment of idiopathic focal segmental glomerulosclerosis

A retrospective control study of low concentration of tacrolimus combined with prednisone in the treatment of idiopathic focal segmental glomerulosclerosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014719
Enrollment
Unknown
Registered
2018-01-31
Start date
2018-02-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

idiopathic focal segmental glomerulosclerosis

Interventions

tacrolimus group:nothing
prednisone group:nothing

Sponsors

the First Affiliated Hospital of Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. All patients were diagnosed with idiopathic focal segmental glomerulosclerosis by clinical and renal biopsy before treatment; 2. proteinuria is greater than 1g/24h; 3. Immunosuppressants were not used within 1 month before starting treatment; 4. All patients were given Angiotensin converting enzyme inhibitors or Angiotensin II receptor 1 blockers; 5. Aged between 12-54 years and sex is not limited.

Exclusion criteria

Exclusion criteria: 1) Hepatitis B, Henoch-Schonlein purpura, systemic lupus erythematosus secondary focal segmental gl omerulosclerosis; 2) Family history of kidney disease and other hereditary nephropathy; 3) Immunosuppressants such as azathioprine, mycophenolate mofetil, cyclosporine A, and leflunomide were taken within 1 month or at the beginning of the study; 4) Contraindications to tacrolimus or high-dose hormones (hepatitis virus carriers, chronic viral hepatitis, any active or serious infection); 5) Medication is not standardized or the treatment time is less than 6 months; 6) Tumor or other serious cases of patients.

Design outcomes

Primary

MeasureTime frame
Proteinuria of 24 hour;

Secondary

MeasureTime frame
concentration of tacrolimus;remission rate;Recurrence rate;

Countries

China

Contacts

Public ContactHongwen Zhao
358984844@qq.com+86 13983360655

Outcome results

None listed

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