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Optimal use of ciclosporin in idiopathic membranous nephropathy associated with nephrotic syndrome

Optimal use of ciclosporin in idiopathic membranous nephropathy associated with nephrotic syndrome - Optimal use of ciclosporin in membranous nephropathy (OCIM-NS study)

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001099
Enrollment
50
Registered
2008-03-31
Start date
2007-10-01
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

idiopathic membranous nephropathy associated with nephrotic syndrome

Interventions

Steroid group: Immunosuppressive therapy is started by predonisolone 0.8mg/kg/day (max 60mg/day). The dose is decreased by 5mg/day in 2 to 4 weeks after remission. The cases who do not reach remission

Sponsors

Division of Kidney and Dialysis, Department of Internal Medicine,Hyogo College of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The cases of idiopathic membranous nephropathy associated with nephrotic syndrome are included in this study. (Diagnosis is done under the criteria of research group of Ministry of Health, Labour and Welfare.) Written informed concent is needed.

Exclusion criteria

Exclusion criteria: The cases who are considered inappropriate under "Guideline of ciclosporin therapy in nephrotic syndrome" or each doctor's decisions.

Design outcomes

Primary

MeasureTime frame
quantity of urinary protein, frequency of relapse, renal function (serum Cr, estimated GFR),time to remission, total dose of steroid (until remission)

Secondary

MeasureTime frame
adverse effects of steroid and ciclosporin, total dose of steroid (in all treatment period), duration of hospitalization, serum albumin, serum total protein, serum total cholesterol, degree of edema

Countries

Japan

Contacts

Public ContactMasaaki Izumi

Hyogo College of Medicine Division of Kidney and Dialysis, Department of Internal Medicine

izumi@hyo-med.ac.jp0798-45-6521

Outcome results

None listed

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