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The prospective multi-center study on the efficacy and safety of mizoribine for the treatment of aged nephrotic patients with primary membranous nephropathy.

The prospective multi-center study on the efficacy and safety of mizoribine for the treatment of aged nephrotic patients with primary membranous nephropathy. - The study on efficacy and safety of mizoribine for the aged patients with membranous nephropathy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008919
Enrollment
200
Registered
2012-09-14
Start date
2012-09-15
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

The patients with nephrotic syndrome due to primary membranous nephropathy.

Interventions

Treatment with a combination of mizoribine plus steroid therapy Treatment with steroid monotherapy

Sponsors

The study group of treatment for aged patients with nephrotic syndrome.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient whose age is more than 65 years old, and who clears all of the following entry-criterion can enroll in this study. 1) The patient is established the diagnosis of nephrotic syndrome. 2) The diagnosis of membranous nephropathy is also histologically established. 3)The eGFR is more than 45ml/min.

Exclusion criteria

Exclusion criteria: Case that showed at least one of the following terms should be excluded. 1) Patient who have the allergy for mizoribine. 2) Data of WBC count before entry showed less than 3000/microL. 3) Patient who has the severe disease, such as heart and liver diseases. 4) Patient who has the severe bacterial, fungal or viral infection. 5) Patient who has the relapsed nephrotic syndrome. 6) Patient who experienced kidney transplantation. 7) The doctor decides that the patient is inappropriate to enroll in this study.

Design outcomes

Secondary

MeasureTime frame
1.Rate of continuity of the selected treatment. 2. The reduction of the degree of proteinuria. 3.Frequency of adverse complication derived from drug use. 4.Total dose of corticosteroid for treatment of nephrotic syndrome. 5. Changes in the renal function.

Primary

MeasureTime frame
Rate of remission from nephrotic syndrome

Countries

Japan

Contacts

Public ContactHajime Hasegawa

The study group of treatment for aged patients with nephrotic syndrome. Affair

hase2126@saitama-med.ac.jp049-228-3604

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026