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临床试验/CTRI/2022/04/042091
CTRI/2022/04/042091进行中(未招募)1 期

An open label safety and efficacy study of a polyherbal local anaesthetic parenteral formulation by estimating pharmacokinetic parameters in healthy adults

Pankajakasthuri Herbals India Pvt Ltd0 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
1 期
状态
进行中(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

  • Healthy volunteers
  • Has a legally acceptable representative capable of under standing the informed consent documents and providing consent on the participants behalf
  • Normal laboratory values in CBC, LFT and RFT
  • Non smokers, non substance abusers, non alcoholic

排除标准

  • 1.Pregnant or breastfeeding women.
  • 2.Body mass index superior to 35ââ?¬â?°kg/m2.
  • 3.Allergy to any one of the ingredients in the formulation.
  • 4.Uncontrolled hypertension/congenital heart problems.
  • 5.Life-threatening comorbidities.
  • 6.Adults legally protected (under judicial protection, guardianship or supervision) and persons deprived of their liberty.
  • 7.Those who are taking regular medication
  • 8.Any other chronic illness

研究者

发起方
Pankajakasthuri Herbals India Pvt Ltd

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Clinical study to find out the safety and efficacy... | 临床试验