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A clinical trial to study the effects of two drugs, Shigru kwatha and Livogrit in patients with Non Alcoholic Fatty Liver Disease

Phase 2
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
Objective Criteria <br/ ><br>1. Ultrasonography whole abdomen <br/ ><br>Timepoint: 0th day 60th day
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