A clinical trial to study the effects of two drugs, Shigru kwatha and Livogrit in patients with Non Alcoholic Fatty Liver Disease
- Conditions
- Health Condition 1: K759- Inflammatory liver disease, unspecified
- Registration Number
- CTRI/2023/10/058382
- Lead Sponsor
- Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patient between the age group of 18 to 65 years will be selected.
2. Patient irrespective of gender, religion, occupation and chronicity will be selected for the study.
3. Both fresh and treated cases would be taken for the study.
4. Patient with Grade 1 and Grade 2 fatty liver only will be selected for the study.
5. Individual with controlled Diabetes Mellitus having Grade 1 and Grade 2 fatty liver will be selected for the study.
1.Pregnant or lactating women will be excluded.
2. Patient who have had Hepatitis B,C or other hepatic viral infection , autoimmune hepatitis and drug induced hepatitis or alcoholic hepatitis will be excluded.
3. Patient with severe complication of the cardiovascular, renal or hematopoietic systems and mental disease will be excluded.
4. Patient will be excluded having decompensated liver disease.
5. Patient with prolonged or a history of ascites , developed Hepatocellular carcinoma Hepatic Encephalopathy , Variceal bleeding will be excluded.
6. Patient with a history of using IFN or antiviral agents or Corticosteroids or Immunosuppresive drugs will also be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Subjective criteria <br/ ><br>1. Anorexia <br/ ><br>2. Fatigue <br/ ><br>3. Abdominal pain <br/ ><br>4. Malaise <br/ ><br>5. Indigestion(avipaka) <br/ ><br>6. Polydipsia (pipasa) <br/ ><br>7. Constipation <br/ ><br>8. Vomiting (chhardi) <br/ ><br>9. Fever (mridu jwara) <br/ ><br>10. Flatulence (aanaha) <br/ ><br>11. TastelessnessTimepoint: 0th day 30th day 60th day
- Secondary Outcome Measures
Name Time Method Objective Criteria <br/ ><br>1. Ultrasonography whole abdomen <br/ ><br>Timepoint: 0th day 60th day