To Evaluate The Efficacy Of Ayurvedic Compound In Hepatobilliary Lithiasis With Special Reference To The Histological Changes & The Biochemical Analysis Of Bile

IMS BHU1 个研究点分布在 1 个国家目标入组 20 人开始时间: 2016年12月30日最近更新: 2018年1月3日

试验速览

阶段: 2 期
状态: 进行中（未招募）
发起方
入组人数: 20
试验地点: 1
主要终点: LFT, Histopathological changes, Bile analysi

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The studt is non randomised, open label, placebo control, single centre trial to evaluate the efficacy of an ayurvedic compound in hepatobiliary lithiasis w.s.r to histopathologigal changes and biochemical analysis of bile.

研究设计

研究类型: Observational

入排标准

年龄范围: 30.00 Year(s) 至 60.00 Year(s)（—）
性别: All

入选标准

•Patients presenting with symptoms like 1.pain in right upper quadrant of abdomen, 2.referring pain to the inferior angle of scapula,
•vomiting,
•flatulent dyspepsia, 6.recurrent indigestion and
•also asymptomatic patients who are diagnosed to have gallstones, accidentally by USG.

排除标准

•1.Patients with gallstones associated with complication such as carcinoma of gallbladder, liver failure, acute pancreatitis.
•2.Uncontrolled other systemic disorders.
•3.Child age group 4.Pregnant lady 5.Immunocompromised patients.
•6.HIV & HbsAg +ve patients.

结局指标

主要结局

LFT, Histopathological changes, Bile analysi

时间窗: 0ne month

次要结局

未报告次要终点

研究者

发起方

IMS BHU

申办方类型

Research institution and hospital

研究点 (1)

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