CTRI/2015/01/005395已完成未知
A PROSPECTIVE, RANDOMIZED, DOUBLE BLIND, PARALLEL GROUP, PLACEBO CONTROLLED CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF Oâ??LIVER -T IN PATIENTS WITH HEPATITIS A VIRUS.
SBL PVT LTD0 个研究点目标入组 100 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
- 100
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
- •Male and female subjects18- 40 years of age
- •Patients having acute virus A hepatitis in the serum.
- •Willing to provide written informed consent along with audio video visual
- •Subjects willing to comply with all the study procedure and requirements
排除标准
- •Who had HBsAg in the serum
- •Patients who had history of ingesting hepatotoxic drugs prior to the onset of symptoms.
- •Women with childbearing Potential and insufficient contraception.
- •Female who is pregnant, planning a Pregnancy (during the course of the study) or
- •nursing a child.
- •Any contraindication to blood sampling.
- •History of HIV Positive serology.
研究者
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