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Study to evaluate the efficacy of Parikara Yoga (An Ayurvedic polyherbal formulation) and Dietary regimen in the Management of Non-Alcoholic Fatty Liver Disease (NAFLD)

Phase 2
Conditions
Health Condition 1: K760- Fatty (change of) liver, not elsewhere classifiedHealth Condition 2: K760- Fatty (change of) liver, not elsewhere classifiedHealth Condition 3: K77- Liver disorders in diseases classified elsewhere
Registration Number
CTRI/2023/08/055977
Lead Sponsor
ational Institute of Ayurveda Deemed to be University, Jaipur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients of either sex of age group >18years and <60 years with USG

finding suggestive of fatty liver grade 1,2 and 3.

2.Non-Alcoholic or patients with history of alcohol addiction less than 20gm

per day in men and 10 gm per day in women.

3. Clinical sign and symptoms suggesting of Yakrita Roga/NAFLD that is,

pain in right upper quadrant/ epigastric region of abdomen, feeling of nausea,

heaviness in abdomen, flatulence ,loss of appetite and burning sensation in

abdomen if any.

4. Patients with normal serum bilirubin level and ALT/AST level less than 1.5

times of normal limit.

5. Patients with/without raised lipid profile.

Exclusion Criteria

1. Pregnant and lactating women.

2. Patients with history of diabetes mellitus, autoimmune hepatitis, drug

abuse, chronic Hepatitis, raised ALT/AST level more than 1.5 times of

normal limit.

3. Patients with complications of metabolic syndrome such as

cerebrovascular accident, myocardial infarction, chronic kidney diseases,

suffering from cirrhosis, ascites, variceal haemorrhage, coagulopathy,

hepatorenal syndrome

4. Patient have any kind of malignancy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in USG findings and grading at the end of 56 daysTimepoint: Changes in USG findings and grading at the end of 56 days
Secondary Outcome Measures
NameTimeMethod
1.Changes in liver function test, lipid profile at the and of 56 days <br/ ><br>2. Changes in clinical sign and symptoms if any at the end of 60 daysTimepoint: At the end of 56 days
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