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临床试验/NCT03170323
NCT03170323Unknown4 期

A Prospective Randomized, Controlled Trial of Mycophenolate Mofetil Plus Steroid in the Treatment Of Patients With Progressive Idiopathic Membranous Nephropathy

Guangdong Provincial People's Hospital1 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2018年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
128
试验地点
1
主要终点
Complete Remission

研究概览

简要总结

Idiopathic membranous nephropathy (IMN) remains a common cause of the nephrotic syndrome in adults. There are few randomized clinical trials regarding the therapeutic effect of mycophenolate mofetil in patients with Idiopathic membranous nephropathy. This study aims to evaluate whether treatment with mycophenolate mofetil is non-inferior to cyclosporins in inducing long-term remission (complete or partial) of proteinuria in patients with idiopathic membranous nephropathy.

详细描述

Idiopathic membranous nephropathy is the most common cause of nephrotic syndrome in adults. In recent year, IMN remains one of the most common glomerular diseases. Long-term remission and stable renal function can prevent idiopathic membranous nephropathy from progressing to end-stage renal disease. Cyclosporine and cyclophosphamide are recommended to be first-line treatment regimen. Corticosteroid is the basic combined drug in the treatment of idiopathic membranous nephropathy. Mycophenolate mofetil is a recently developed immunosuppressive agent with fewer renal toxicity than cyclosporin.Besides, high dose prednisone may be effective for patients in Asia according to literatures from Asia. In our study, patients with idiopathic membranous nephropathy would be treated with mycophenolate mofetil and high dose prednisone,whose outcome will be compared with cyclosporin and low dose prednisone. We aims to evaluate whether treatment with mycophenolate mofetil is non-inferior to cyclosporins in inducing long-term remission of proteinuria in patients with idiopathic membranous nephropathy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 1.Patients who provided informed consent
  • 2.Patients who are diagnosed as membranous nephropathy by renal biopsy,and other secondary factors are excluded
  • 3.18 years of age or older, male or female
  • 4.24 hours urine protein or spot urine protein/creatinine ratio > 8.0 g/day at least for twice confirmed
  • 5.The patients that satisfy more than three of following items are included even if proteinuria is less than 8 grams per day:
  • estimated glomerular filtration rate(eGFR) < 60 ml/min/1.73m2
  • Hypertension (BP above 140/90millimetre of mercury or BP above 120/80millimetre of mercury in patients taking anti-hypertensive agents)
  • 24 hours urine protein or spot urine protein/creatinine ratio > 5.0 g/day
  • Serum albumin (g/dL) < 3.0

排除标准

  • 1.Severe infective disease
  • 2.Allergy history to clinical trial medication and acute or chronic allergy for 4 weeks recently.
  • 3.Clinical history of treatment with other immunosuppressive medication
  • 4.Probability of pregnancy, breast feeding woman
  • 5.Uncontrolled hypertension (more than 160/100 millimetre of mercury )
  • 6.estimated glomerular filtration rate(eGFR)<30 ml/min/1.73m2。
  • 7.Abnormal liver function test (more than 3 times above compared with normal value)
  • 8.Absolute neutrophil count <1,500/mm3 or leukocyte <2,500/mm3 or platelets <100,000/mm3
  • 9.Secondary membranous nephropathy
  • 10.Expected life expectancy is less than 1 year
  • 11.The researchers evaluated that the patient's compliance was not appropriate for the trial
  • 12.Previous or present history of cancer and have risk of recurrence or metastasis

研究组 & 干预措施

Mycophenolate mofetil

Experimental

Drug: Mycophenolate mofetil, high dose steroid Duration: 1 year

干预措施: Mycophenolate Mofetil (Drug)

Cyclosporin

Active Comparator

Drug: Cyclosporin, low dose steroid Duration: 1 year

干预措施: Cyclosporins (Drug)

结局指标

主要结局

Complete Remission

时间窗: after treatment for 1 year.

Urinary protein excretion\<0.3 g/d (uPCR\<300 mg/g or \<30 mg/mmol), confirmed by two values at least 1 week apart, accompanied by a normal serum albumin concentration, and a normal serum creatinine.

Partial Remission

时间窗: after treatment for 1 year.

Urinary protein excretion \<3.5 g/d (uPCR \<3500 mg/g or \<350 mg/mmol) and a 50% or greater reduction from peak values;confirmed by two values at least 1 week apart, accompanied by an improvement or normalization of the serum albumin concentration and stable serum creatinine.

次要结局

  • estimated Glomerular Filtration Rate(after treatment for 1 year)
  • serum creatinine(after treatment for 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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