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临床试验/ISRCTN17242711
ISRCTN17242711已完成未知

INdian COntrolled trial of RITuximab vs Modified Ponticelli regimen for treatment of primary membranous nephropathy

Muljibhai Patel Urological Hospital0 个研究点目标入组 68 人开始时间: 2022年4月15日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
68

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Patients older than 18 years who provide written informed consent.
  • 2. Biopsy-proven primary MN within 2 years of enrolment with nephrotic range proteinuria denoted by 24-hour urine protein =3.5 g or UPCR (urine protein:creatinine ratio) =3500 mg/g as well as the following:
  • 2.1. Serology or biopsy positive for AntiPLA2R
  • 2.2. Serology or biopsy negative for AntiPLA2R and secondary causes ruled out
  • 2.3. Evaluation for secondary causes was done in all patients, even in patients who were positive for Anti-PLA2R antibodies on serology or PLA2R antigen on biopsy because these have also been found in some cases of secondary MN
  • 3. Estimated GFR =30 ml/min/1.73m². The CKD-EPI creatinine equation was used for the calculation of the eGFR
  • 4. Treatment with an ACEI or ARB for at least 3 months before enrolment

排除标准

  • 1. Secondary MN
  • 2. Active serious infections
  • 3. Pregnant women
  • 4. Suspected or known hypersensitivity to either interventional drug
  • 5. Patients with persistently low estimated GFR <30 ml/min/1.73m² in the absence of acute causes such as acute tubular injury, renal vein thrombosis and others

研究者

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