Skip to main content
Clinical Trials/IRCT20100524004010N39
IRCT20100524004010N39
Recruiting
Phase 2

The effect of co-administration of Dietary Approaches To Stop Hypertension (DASH) and Intermittent Fasting (IF) diets on hepatic parameters, glucose homeostasis, lipid profile and inflammatory biomarkers in patients with Non-Alcoholic Fatty Liver Disease (NAFLD): a Randomized Control Trial

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
on-alcoholic fatty liver.
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
50
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age over 18 years
  • Having evidence of non\-alcoholic fatty liver in fibroscan (CAP score\>260\)
  • Not having a history of alcohol consumption or alcohol consumption less than 10 grams per day in women and less than 20 grams per day in men.
  • Not taking drugs that affect blood lipids, metformin, vitamin E and ursodeoxycholic acid (UDCA) and hepatotoxic drugs such as phenytoin, amoxifen and lithium.
  • Not having chronic and acute liver diseases (hepatitis B, C, etc.), biliary disease, known autoimmune diseases, cancer and hereditary disorders affecting the liver (iron, copper storage disease)
  • No history of weight loss surgery, weight loss program in the last 3 months
  • Non\-adherence to special diets such as vegetarianism
  • No history of uncontrolled thyroid disease
  • Willingness to participate in the studuy
  • Not having uncontrolled celiac disease, diabetes, cardiovascular disease, lung disease and kidney disease

Exclusion Criteria

  • History of weight loss surgery and weight loss program during the last 3 months
  • Failure to accept study conditions
  • Taking medicine or supplements that can affect the results
  • Following special diets and vegetarianism during the last 3 months
  • Pregnancy or breastfeeding in women or Using birth control pills

Outcomes

Primary Outcomes

Not specified

Similar Trials