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Effect of the Root Extract of Cichorium Intybus Formula on Fatty liver disease

Effect of the Root Extract of Cichorium Intybus Formula on Reducing Alanine Aminotransferase (ALT) in Non-alcoholic Fatty Liver Disease: A Randomized Double-blind Clinical Trial Including Placebo

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013121615825N1
Enrollment
60
Registered
2014-06-09
Start date
2014-02-20
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

Fatty liver disease. Diseases of liver

Interventions

Intervention 1: Intervention 1: A capsule containing 500 mg of Cichorium intybus root extract is given to the patients group in the morning before breakfast. Intervention 2: Intervention 2: Two capsul
Treatment - Drugs
Intervention 1: A capsule containing 500 mg of Cichorium intybus root extract is given to the patients group in the morning before breakfast.
Intervention 2: Two capsules containing corn starch are given to the control group.

Sponsors

School of Traditional Medicine, Traditional Medicine and Materia Medica Research Center Shahid Behes
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion / Exclusion : Inclusion Criteria: Patient age of 18 to 70 years; fatty liver disease grade 1, 2 or 3 diagnosed by ultrasound; No current use of another drug for fatty liver treatment which has not been taken before. Exclusion Criteria :Advanced cardiovascular diseases, pulmonary or renal diseases; Pregnancy; Breast feeding; Allergy to Cichorium intybus; Non-compliance with medication; Psychiatric diseases complicating the results evaluation or causing patient’s lack of cooperation; Advanced cirrhosis; Hepatitis and other liver diseases except non-alcoholic fatty liver; alcohol consumption by patients; Fatty acid oxidation disorder ( congenital ); Patients with diabetes who are treated with insulin.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Alanine Aminotransferase. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.

Secondary

MeasureTime frame
Aaspartat Aminotransferase. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Fasting blood sugar. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Total Cholesterol. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Triglycerides. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;High-density lipoprotein. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Low-density lipoprotein. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Platelets. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Albumin. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Glucose tolerance test. Timepoint: Before intervention and two months after intervention. Method of measurement: Spectrophotometer.;Body Mass Index. Timepoint: Before intervention and two months after intervention. Method of measurement: Scale and Meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Nikkhajooei

School of Traditional Medicine, Traditional Medicine and Materia Medica Research Center Shahid Behes

m_niknik@yahoo.com+218 8773522

Outcome results

None listed

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