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The effect of Sitaglyptin and placebeo in the treatment of non-alcoholic fatty liver disease

A comparison between Sitaglyptin and placebeo in the treatment of non-alcoholic fatty liver disease : A tripple blind randomized clinical trials

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140430017505N2
Enrollment
120
Registered
2020-07-20
Start date
2019-02-24
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Non-alcoholic fatty liver. Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: Intervention group: In addition to lifestyle recommendations, they will receive a daily dose of 50 mg of Sitagliptin manufactured by Tehran Daroo Company for one year. Intervention 2:

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: People over the age of 18 who are diagnosed with grade 2 or 3 fatty liver on primary ultrasound for patients. People with liver enzymes with ALT above 30 in women and above 40 in men.

Exclusion criteria

Exclusion criteria: Evidence of viral hepatitis (such as hepatitis B surface antigen positive and RNA positive for hepatitis C) Medicinal hepatitis and autoimmune hepatitis HbA1C hemoglobin level higher or equal to 5.6% History of diabetes Wilson's Disease A history of diabetes (fasting blood sugar high or equal to 126 mg / dL) Hemochromatosis Regular consumption of alcohol Evidence of untreated liver cirrhosis and severe liver disease APRI above or equal to 2 Patients who were already treated with sitagliptin or vitamin E

Design outcomes

Primary

MeasureTime frame
Biochemical tests (ALT, AST, ALKP, GGT, Bili total, Bili Direct, FBS, Insulin, Ferritin, HDL, LDL, TG, Chol). Timepoint: Before and after treatment. Method of measurement: Test.;Hematological tests. Timepoint: Before and after treatment. Method of measurement: Test.;Demographic characteristics. Timepoint: Before and after treatment. Method of measurement: Questionnaire.;Fatty liver grade. Timepoint: Before and after treatment. Method of measurement: Device Fibrous Scan.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Nejadisalami

Iran University of Medical Sciences

a.nezhadisalami@gmail.com+98 21 8214 1711

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 11, 2026