跳至主要内容
临床试验/CTRI/2008/091/000060
CTRI/2008/091/000060招募中3 期

â??An Open Labelled, Double Arm, Randomized, Multicentric, Prospective And Comparative, Phase-III Trial To Evaluate The Safety And Efficacy Of Fixed Dose Combination Of Ceftriaxone And Vancomycin Injection Vs. Vancomycin Injection In Subjects With Various Bacterial Infections.â??

Venus Remedies Limited0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
200

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

  • All subjects aged between 18 and 70 years.
  • Diagnosed subjects of infectious disease (on clinical evaluation).
  • Subjects willing to give informed consent.
  • Subject suffering from any of the following infections- Lower respiratory tract infections, skin and skin structure infections, endocarditic, bacterial meningitis and bone infection.

排除标准

  • History of hypersensitivity reaction or any specific contraindication to penicillin group of drugs or Ceftriaxone or Vancomycin.
  • Presence of hepatic or renal disorder
  • Pregnancy&/or lactation

研究者

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