CTRI/2022/11/047684
Not yet recruiting
未知
Efficacy of Intermittent fasting in patients with non-alcoholic fatty liver disease.
Dr Deepankshi Aggarwal0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: K760- Fatty (change of) liver, not elsewhere classified
- Sponsor
- Dr Deepankshi Aggarwal
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) NAFLD patients will be defined by the evidence of hepatic steatosis, either by ultrasound or Fibroscan with no significant alcohol consumption (less than 20g/day) and after excluding alternate causes of steatosis and/or raised hepatic transaminases (including but not limited to drug intake, chronic Hepatitis B and C, autoimmune hepatitis, hemochromatosis, Wilsonâ??s disease, celiac disease).
- •2\) Overweight and Class I Obese patients as per Asia\-Pacific criteria (BMI greater than or equal to 23 ,and less than 30 Kg/m2\).
- •3\) Consent to participate in study.
Exclusion Criteria
- •1\) Patients who are not willing to give consent for the study.
- •2\) Patients having Type 2 Diabetes mellitus.
- •3\) Patients who have evidence of cirrhosis liver on ultrasound or Fibroscan (LSM greater than or equal to 12\.5 kPa).
- •3\) Patients with history of hepatic decompensation.
- •4\) Patients with class II obesity as per Asia\-Pacific criteria (BMI greater than or equal to 30 Kg/m2\).
- •5\) Patients taking weight loss drugs.
- •6\) Patients taking pharmacotherapy for NASH (e.g. Pioglitazone, Vit E and Saroglitazar).
- •7\) Patients with post bariatric surgery status.
- •8\) Pregnant / lactating females. Those non pregnant female patients recruited in the study who will conceive during the study period will be excluded from the study.
Outcomes
Primary Outcomes
Not specified
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