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Clinical study for tacrolimus monotherapy in nephrotic idiopathic membranous nephropathy.

The efficiency and side effects of tacrolimus monotherapy in the treatment of nephrotic idiopathic membranous nephropathy.

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021314
Enrollment
Unknown
Registered
2019-02-13
Start date
2013-01-01
Completion date
Unknown
Last updated
2019-02-18

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

Conditions

idiopathic membranous nephropathy

Interventions

Case series:TAC monotherapy

Sponsors

Tianjin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 72 Years

Inclusion criteria

Inclusion criteria: (1) aged between 18 and 75 years; (2) a biopsy proven IMN (stage I–IV); (3) meet one of the following conditions: urinary protein excretion of =3.5 g/24 h with hypoalbuminemia, or serum albumin of =30 g/L with urinary protein of >2.0 g/24 h. All the above abnormalities lasted at least 3 months without spontaneous remission; (4) initial serum creatinine level of <133µmol/L; (5) no immunosuppressive agents used in the previous 6 months.

Exclusion criteria

Exclusion criteria: (1) secondary membranous nephropathy, such as systemic lupus erythematosus; (2) malignant tumor; (3) infection, such as hepatitis B or C virus infection and tuberculosis; (4) pregnancy or lactating; (5) received corticosteroid and/or immunosuppressive agents in the previous 6 months; (6) coexistence of life-threatening complications, such as heart failure, severe infection or active gastrointestinal bleeding; (7) poor compliance.

Design outcomes

Primary

MeasureTime frame
remission rate;

Secondary

MeasureTime frame
changes in proteinuria;changes in serum albumin;changes in serum creatinine;changes in serum uric acid;side effects;

Countries

China

Contacts

Public ContactYang Dingwei

Tianjin Hospital

dwyang2016@126.com+86 022 60910675

Outcome results

None listed

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