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临床试验/CTRI/2018/04/013278
CTRI/2018/04/013278已完成未知

Comparative study of efficacy of Plasma Exchange and Intra Venous Immunoglobulin(IVIG)in patients of Guillain Barre Syndrome

Department of Transfusion Medicine PGIMER0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
40

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

  • GBS patient chosen for the study purpose within four weeks of onset of weakness following Ausbury criteria and ranging from 13 to 60 years of age.

排除标准

  • 1. Duration of illness more than 30 days before entry in study.
  • 2. Children less than or equal to 12 year of age.
  • 3. Any contraindication for IVIG or TPE.
  • 4. Patient with hypokalemia and porphyria.
  • 5. Specific exclusions with atypical features such as--
  • a.Purely sensory symptoms.
  • b.Cranial nerve palsies without significant limb weakness.
  • c.Previous acute polyneuropathy.
  • d.Improvement of one or more disability grades before inclusion
  • e.Pregnancy.
  • f. Previous therapy with immunosuppressive drugs other than steroids.
  • g. Previous plasmapheresis / IVIG therapy.
  • h. Patient not willing to participate in the study

研究者

发起方
Department of Transfusion Medicine PGIMER

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