跳至主要内容
临床试验/CTRI/2012/08/002850
CTRI/2012/08/002850已完成3 期

Evaluation of hepatoprotective effect of Picroliv in patients receiving multi drug therapy for Tuberculosis.

CSIR Central Drug research Institute0 个研究点目标入组 260 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
260

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

  • 1 Patients over the age of 16 years.
  • 2 Willing to give informed consent and comply with protocol requirements and follow up.
  • 3 Diagnosed as Category I, II or III tuberculosis of the RNTCP (Revised National Tuberculosis Control Program).
  • 4 Receiving treatment with at least 3 anti tubercular drugs or as per the RNTCP guidelines.

排除标准

  • 1 Unwilling to comply with protocol requirements and duration of follow up.
  • 2 History of jaundice in the past 6 months.
  • 3 History of having received any drug from the non allopathic systems of medicine in the past 3 months.
  • 4 Pregnancy.
  • 5 Severe hepatic, renal or cardiac disease.
  • 6 H/o consuming alcohol daily.

研究者

发起方
CSIR Central Drug research Institute

相似试验