Clinical Trials Directory

Trials / Completed

CompletedNCT02983669

The Effects of Zataria Multiflora Boiss (Shirazi's Thyme) on Nonalcoholic Fatty Liver Disease

The Effects of Zataria Multiflora Boiss (Shirazi's Thyme) on Biochemical Markers and Imaging Studies of Patients With Nonalcoholic Fatty Liver Disease (NAFLD)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
86 (actual)
Sponsor
Shiraz University of Medical Sciences · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to evaluate the effects and safety of a dietary supplement, Zataria multiflora Boiss (Shirazi's Thyme) in the treatment of non alcoholic fatty liver disease (NAFLD).

Detailed description

In a randomized double-blind placebo-controlled clinical trial Shirazi's Thyme is compared with placebo. Investigators select randomly 90 patients with NAFLD by inclusion criteria. Investigators measure anthropometric and laboratory parameters including fasting blood sugar, insulin, liver enzymes, lipid profile, and grade in sonography before intervention and 90 days later. Patients are divided into two equal groups. Intervention group in addition to diet and exercise recommendations receive capsules containing 700 mg of Shirazi thyme powder daily for 90 days. Placebo group in addition to the same recommendations for diet and exercise, receives placebo capsules twice daily.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTThymeThyme capsule 350 mg twice daily
OTHERPlaceboPlacebo capsule 350 mg twice daily

Timeline

Start date
2017-01-01
Primary completion
2017-04-20
Completion
2017-05-10
First posted
2016-12-06
Last updated
2017-10-04

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT02983669. Inclusion in this directory is not an endorsement.