CTRI/2014/02/004410已完成2 期
A Randomized, Active Controlled, Multicentre, Prospective, Clinical Study to Compare the Efficacy and Safety of Dabur Hepano Tablet with a Marketed Liver Formulation in Liver Disorder Patients with Abnormal Liver Function Test (LFT)
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 180
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
- •Willing to provide informed consent to participate in the study
- •Males or females 18-65 years of age.
- •Diagnosis of hepatic disorder with abnormal LFT and clinical icterus
- •Serum total bilirubin level more than equal to 2 mg/dL, AST or ALT >2 times ULN
- •The subject is able and willing to undertake all study-required procedures and has the ability to take oral medications
排除标准
- •Pregnant or lactating mother
- •Suspected hypersensitivity to contents of investigational product liver formulation
- •Known case of hepatitis-B or hepatitis-C
- •Obstructive Jaundice and Advanced liver diseases
- •Subjects with serious illness,
- •Current use of other herbal medicines for liver disorders or recent use within past two weeks
- •Other conditions, which in the opinion of the investigators, makes the patient unsuitable for enrollment or could interfere with his/her participation in, and completion of the protocol
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