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Clinical Trials/CTRI/2022/11/047684
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
Dr Deepankshi Aggarwal

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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