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The effect of Shirazi thyme in the treatment of fatty liver

The effect of Zataria multiflora Boiss in the treatment of non alcoholic fatty liver disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120925447N1
Enrollment
90
Registered
2016-10-16
Start date
2016-05-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non alcoholic fatty liver. Non alcoholic fatty liver disease

Interventions

Intervention 1: Intervention group : 700 mg (two 350 mg cap ) Shirazi thyme powder bid for 90 days. Intervention 2: Control group : 700 mg (two cap 350 mg ) wheat powder bid for 90 days.
Treatment - Drugs
Placebo
Intervention group : 700 mg (two 350 mg cap ) Shirazi thyme powder bid for 90 days
Control group : 700 mg (two cap 350 mg ) wheat powder bid for 90 days

Sponsors

Vice chancellor for research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: signed informed consent; age between 20 to 65 years old; BMI : 18 - 35; evidence of fatty liver in sonography; ALT equal or more than 45 in male and equal or more than 29 in female. Exclusion criteria: pregnancy; lactation; alcohol consumption; diabetes mellitus; history of allergic reaction to Thyme; acute or chronic hepatic disease; treated or untreated malignancy; consumption of hepatotoxic drugs during six months ago or less; consumption of drugs with effect on the biochemical markers of this study during three months ago or less; hyper or hypothyroidism; renal insufficiency (Cr > 1.5 ).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Alaninaminotransferase. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Grade of fatty liver. Timepoint: Before intervention and three months after intervention. Method of measurement: Ultrasonography.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Before intervention and three months after intervention. Method of measurement: By manometer according to mmHg.;Fasting blood sugar. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Aspartateaminotransferase. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Body mass index. Timepoint: Before intervention and three months after intervention. Method of measurement: Scale and measuring tape.;Waist circumference. Timepoint: Before intervention and three months after intervention. Method of measurement: By measuring tape.;Hip circumference. Timepoint: Before intervention and three months after intervention. Method of measurement: By measuring tape.;Insulin. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Lipid profile. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Dokht Zamani

Faculty of Traditional Medicine, Shiraz University of Medical Sciences

nzamani117@yahoo.com+98 71 3635 8186

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026