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A Controlled Study of Steroids Plus Cyclosporin Therapy for Patients of Idiopathic Membranous Nephropathy

Opportunity, Validity and Security of Steroids Plus Cyclosporin Therapy for Patients of Idiopathic Membranous Nephropathy : A Prospective, Randomized, Controlled, Multi-Center Clinical Trial

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02173106
Enrollment
180
Registered
2014-06-24
Start date
2014-06-30
Completion date
2016-12-31
Last updated
2014-07-01

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

Conditions

Cyclosporin Overdose, Idiopathic Membranous Nephropathy, Proteinuria, Spontaneous Remission, Steroid Nephropathy

Brief summary

This prospective, randomized, controlled, multicenter clinical trial will evaluate Opportunity, Validity and Security of Steroids Plus Cyclosporin therapy for patients of Idiopathic Membranous Nephropathy.

Detailed description

Idiopathic membranous nephropathy is a main reason for nephropathy. Since it can get spontaneous remission, in KDIGO, it is recommend that initial therapy should be started only in patients with nephrotic syndrome and when at least the following condition is met:urinary protein excretion persistently exceeds 4g/d and remains at over 50% of the baseline value,and does not show progressive and antiproteinuric therapy during an observation period of at least 6 months. But many retrospective researches reported that using steroids and immunosuppressive agents were better than waiting for spontaneous remission. There were few prospective, randomized, controlled research on whether it is better that begin to use steroids and immunosuppressive agent early without waiting for 6 months. In our study,we evaluate the validity and security of steroids plus cyclosporin therapy in idiopathic membranous nephropathy. This will be a prospective, randomized, controlled, multicenter study. Patients in treatment group will receive oral methylprednisolone 0.4mg/kg/d and 3.5\ 5mg/kg/d cyclosporin for 6 months. Patients in control group will waiting for spontaneous remission for 6 months,if there were no spontaneous remissions, patients in control group will receive oral methylprednisolone 0.4mg/kg/d and 3.5\ 5mg/kg/d cyclosporin for 6 months. After followed-up for 6 months the curative and side effect of steroid plus cyclosporin therapy in the early stage of idiopathic membranous nephropathy will be evaluated.

Interventions

DRUGsteroid & Cyclosporin

oral methylprednisolone 0.4mg/kg/d and Cyclosporin for 6 months

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 14\ 75 years, regardless of gender without secondary reason, idiopathic membranous nephropathy by renal biopsy * Average urinary protein excretion of at least3.5g/24h on two successive examinations,or plasma albumin \<30g/l * eGFR≥40ml/min/1.73m2 * Willingness to sign an informed consent

Exclusion criteria

* Secondary membranous nephropathy such as systemic lupus erythematosus, hepatitis B -associated nephritis * Current or recent (within 30 days) exposure to high-dose of steroids or immunosuppressive therapy (CTX、MMF、CsA、FK506). * Cirrhosis, chronic active liver disease * History of significant gastrointestinal disorders (e.g. severe chronic diarrhea or active peptic ulcer disease) * Any Active systemic infection or history of serious infection within one month. * Other major organ system disease (e.g. serious cardiovascular diseases including congestive heart failure, chronic obstructive pulmonary disease, asthma requiring oral steroid treatment or central nervous system diseases) * Active tuberculosis * Known allergy, contraindication or intolerance to the steroids * Pregnancy or breast feeding at the time of entry or unwillingness to comply with measures for contraception * Malignant tumors * Excessive drinking or drug abuse * Mental aberrations * Current or recent (within 30 days) exposure to any other investigational drugs

Design outcomes

Primary

MeasureTime frame
Remission of proteinuria (complete or partial)up to 6 months

Secondary

MeasureTime frame
Deterioration of renal function (evidenced by a 50% rise from baseline serum creatinine (SCr) levels, or a 25% decline from baseline eGFR levels, or onset of end-stage renal disease or dialysis treatment, or kidney transplantation).up to 6 months

Countries

China

Contacts

Primary ContactZongpei Jiang, MD&Ph D
jx.home@medmail.com.cn8620-38379727

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026