CTRI/2020/07/026362尚未招募不适用
CLINICAL EVALUATION OF THE THERAPEUTIC EFFICACY OF SARVAKALPA-GHAN-VATI IN NON-ALCOHOLIC LIVER DISORDER.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- normalisation of LFT values
研究概览
简要总结
TRIAL NOT YET STARTED
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients between the age group of 18-65 years will be selected.
- •Patients irrespective of sex, religion, occupation and chronicity will be selected for the study.
- •Both fresh and treated cases would be taken for the study.
- •Patients with higher LFT levels than the upper limit of normal value will be selected.
- •Patients with GRADE 1 and GRADE 2 fatty liver will be selected for the study.
- •Patient with controlled Diabetes mellitus having GRADE 1 and GRADE 2 fatty liver will be selected for the study.
排除标准
- •Patients aged <18 years or >65 years will be excluded.
- •Pregnant or lactating women will be excluded.
- •Patients who had hepatitis B, C or other hepatic viral infection, autoimmune hepatitis and drug-induced hepatitis or alcoholic hepatitis will be excluded.
- •Patients with severe complications of the cardiovascular, renal or hematopoietic systems and mental diseases will be excluded.
- •Patients will be excluded having decompensated liver disease.
- •Patients with prolonged or a history of ascites, developed hepato-cellular carcinoma, hepatic encephalopathy, variceal bleeding will be excluded.
结局指标
主要结局
normalisation of LFT values
时间窗: 30 days
次要结局
- Exacerbation in Signs & Symptoms.(30 days)
研究者
研究点 (1)
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