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临床试验/SLCTR/2009/001
SLCTR/2009/001已完成2 期

se of intravenous acetylsalicylic acid (‘Aspirin’) as a novel antidote for human paraquat poisoning- can it reduce the 70% mortality rate and oxidative stress?

Welcome Trust and NHMRC through SACTRC0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
20

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

  • Paraquat self poisoning presenting within 24 hours and a positive urine dithionite test

排除标准

  • Age under 14 years pregnanacy presenting after 24 hours known aspirin allergy

研究者

发起方
Welcome Trust and NHMRC through SACTRC

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se of intravenous acetylsalicylic acid (‘Aspirin’)... | 临床试验