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临床试验/CTRI/2020/12/029849
CTRI/2020/12/029849尚未招募未知

Efficacy and Safety of B Cell Targeted Low Dose Rituximab in Primary Membranous Nephropathy: Prospective Single Arm Interventional Study (A Pilot Study)

il0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

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

入选标准

  • •Patients aged 18 years and older.
  • •Patients with diagnosis of Membranous nephropathy proven with renal biopsy (light microscopy and immunofluorescence microscopy) who are not responsive to conservative therapy after 3 months24 or who develop complications related to nephrotic syndrom.11
  • •Newly diagnosed patients or previously treated patients of membranous nephropathy presenting with relapse.
  • •Estimated GFR >=30 mL/min/1.73 m2 (CKD-EPI formula).

排除标准

  • •Patients with underlying disorder (e.g. Hepatitis B and C, HIV, Systemic Lupus Erythematosus, medications causing membranous nephropathy, malignancies).
  • •History of hypersensitivity or allergic reaction to rituximab.
  • •Patients with life threatening complications of nephrotic syndrome like pulmonary embolism.
  • •Patients with rapid deterioration of renal function, not explained otherwise.
  • •Active infection/sepsis.
  • •Pregnancy or breast feeding.

研究者

发起方
il

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