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Clinical assessment of tacrolimus in treating patients with membranous nephropathy: A protocol for systematic review and meta-analysis

Clinical assessment of tacrolimus in treating patients with membranous nephropathy: A protocol for systematic review and meta-analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200058661
Enrollment
Unknown
Registered
2022-04-13
Start date
2022-04-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

Membranous nephropathy

Interventions

Control group:Other treatment

Sponsors

People’s Hospital of Songzi
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Membranous nephropathy proven by renal biopsy; 2. Nephrotic syndrome, defined as the presence of nephrotic-range proteinuria > 3.5 g/d, serum albumin 60 ml/min per 1.73 m2; 4. No immunosuppressive agents used in the previous 6 months; 5. Follow-up time of at least 24 months; 6. Agree to accept the random assignment, understand and be willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Serious complications such as thrombosis, renal failure and infection; 2. Serious diseases such as HIV, cardiac dysfunction, hepatitis B, hepatitis C or serum amino-transferase exceeding twofold the normal upper limit; 3. Other contraindications to immunosuppressants; 4. Hypersensitivity to macrolide medication; 5. Diabetes mellitus or the coexistence of other severe kidney diseases; 6. Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Complete remission;Partial response;

Secondary

MeasureTime frame
Renal survival;

Countries

China

Contacts

Public ContactZhou Yuan

People’s Hospital of Songzi

zhouyuansz6222278@hotmail.com+86 0716-6222278

Outcome results

None listed

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