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Combination therapy of tacrolimus and intravenous cyclophosphamide for remission induction of lupus nephritis

Not Applicable
Conditions
lupus nephritis
Registration Number
JPRN-UMIN000004893
Lead Sponsor
Department of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
16
Inclusion Criteria

Not provided

Exclusion Criteria

Patients are excluded if they meet any one of the following criteria. 1)Patients whose serum creatinine is 2 mg/dL or more; or creatinine clearance is 30 mL/min/1.73m2 or less. 2)Patients needing steroid pulse therapy. 3)Patients having received intravenous cyclophosphamide or steroid pulse therapy within 6 months of the start of the study. 4)Patients having suffered from hypersensitivity against the ingredients of tacrolimus capsules. 5)Patients administered with cyclosporine or bosentan. 6)Patients administered with potassium sparing diuretics. 7)Patients pregnant or suspected to be pregnant; or breast-feeding; or expecting to be pregnant during the study period. 8)Patients administered with pentostatin. 9)Patients having suffered from hypersensitivity against the ingredients of injectable cyclophosphamide. 10)Patients having a serious infectious disease. 11)Patients considered ineligible by a doctor in charge for other reason.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete remission rate at 6 months after the start of protocol treatment
Secondary Outcome Measures
NameTimeMethod
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