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

Primary Purpose

Idiopathic Membranous Nephropathy, Proteinuria, Spontaneous Remission

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
steroid & Cyclosporin
Sponsored by
Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Membranous Nephropathy

Eligibility Criteria

14 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Department of Nephrology,Dongguan People's HospitalRecruiting
  • Department of Nephrology, 2nd Affiliated Hospital,Guangzhou Medical UniversityRecruiting
  • Department of Nephrology, 6th Affiliated Hospital, Sun Yat-Sen UniversityRecruiting
  • Department of Nephrology,Huizhou Municipal Central HospitalRecruiting
  • Department of Nephrology,1st Affiliated Hospital,Shenzhen UniversityRecruiting
  • Department of Nephrology,1st People's Hospital of ZhaoqingRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Group A: steroid & Cyclosporin

Group B: no steroid & Cyclosporin

Arm Description

oral methylprednisolone 0.4mg/kg/d and 3.5~5mg/kg/d cyclosporin for 6 months.

no steroid and cyclosporin and waiting for spontaneous remission for 6 months

Outcomes

Primary Outcome Measures

Remission of proteinuria (complete or partial)

Secondary Outcome Measures

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).

Full Information

First Posted
June 23, 2014
Last Updated
June 30, 2014
Sponsor
Sun Yat-sen University
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1. Study Identification

Unique Protocol Identification Number
NCT02173106
Brief Title
A Controlled Study of Steroids Plus Cyclosporin Therapy for Patients of Idiopathic Membranous Nephropathy
Official Title
Opportunity, Validity and Security of Steroids Plus Cyclosporin Therapy for Patients of Idiopathic Membranous Nephropathy : A Prospective, Randomized, Controlled, Multi-Center Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2014
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Membranous Nephropathy, Proteinuria, Spontaneous Remission, Steroid Nephropathy, Cyclosporin Overdose

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A: steroid & Cyclosporin
Arm Type
Experimental
Arm Description
oral methylprednisolone 0.4mg/kg/d and 3.5~5mg/kg/d cyclosporin for 6 months.
Arm Title
Group B: no steroid & Cyclosporin
Arm Type
No Intervention
Arm Description
no steroid and cyclosporin and waiting for spontaneous remission for 6 months
Intervention Type
Drug
Intervention Name(s)
steroid & Cyclosporin
Intervention Description
oral methylprednisolone 0.4mg/kg/d and Cyclosporin for 6 months
Primary Outcome Measure Information:
Title
Remission of proteinuria (complete or partial)
Time Frame
up to 6 months
Secondary Outcome Measure Information:
Title
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).
Time Frame
up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zongpei Jiang, MD&Ph D
Phone
8620-38379727
Email
jx.home@medmail.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zongpei Jiang, MD &Ph.D
Organizational Affiliation
The Sixth Affiliated Hospital,Sun Yat-Sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Nephrology,Dongguan People's Hospital
City
Dongguan
State/Province
Guangdong
ZIP/Postal Code
523059
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guohui Liu, MD
Phone
86769-28637333
Email
liuguohui5@126.com
First Name & Middle Initial & Last Name & Degree
Guohui Liu, MD
Facility Name
Department of Nephrology, 2nd Affiliated Hospital,Guangzhou Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510260
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jianbo Liang, MD.
Phone
8620-34152282
Email
boliangjian@tom.com
First Name & Middle Initial & Last Name & Degree
Jianbo Liang, MD
Facility Name
Department of Nephrology, 6th Affiliated Hospital, Sun Yat-Sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510655
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zongpei Jiang, MD & Ph. D
Phone
8620-38379727
Email
jx.home@medmail.com.cn
First Name & Middle Initial & Last Name & Degree
Zongpei Jiang, MD & Ph.D
Facility Name
Department of Nephrology,Huizhou Municipal Central Hospital
City
Huizhou
State/Province
Guangdong
ZIP/Postal Code
516001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Weiqiang Zhong, MD
Phone
86752-2288288
Email
13809669766@126.com
First Name & Middle Initial & Last Name & Degree
Weiqiang Zhong, MD
Facility Name
Department of Nephrology,1st Affiliated Hospital,Shenzhen University
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yongcheng He, MD
Phone
86755-83366388
Email
heyongcheng@medmail.com.cn
First Name & Middle Initial & Last Name & Degree
Yongcheng He, MD
Facility Name
Department of Nephrology,1st People's Hospital of Zhaoqing
City
Zhaoqing
State/Province
Guangdong
ZIP/Postal Code
526020
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jinquan Wu, MD
Phone
86758-2832139
Email
zqwujq@163.com
First Name & Middle Initial & Last Name & Degree
Jinquan Wu, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
34778952
Citation
von Groote TC, Williams G, Au EH, Chen Y, Mathew AT, Hodson EM, Tunnicliffe DJ. Immunosuppressive treatment for primary membranous nephropathy in adults with nephrotic syndrome. Cochrane Database Syst Rev. 2021 Nov 15;11(11):CD004293. doi: 10.1002/14651858.CD004293.pub4.
Results Reference
derived

Learn more about this trial

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

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