Skip to content

Novel Antidiabetic Medications and Their Effect on Liver Steatosis (NAMELS-18)

Effect of Dulaglutide vs Empagliflozin on Non-alcoholic Fatty Liver Disease of Patients With Type 2 Diabetes Mellitus

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05946148
Acronym
NAMELS-18
Enrollment
78
Registered
2023-07-14
Start date
2018-06-01
Completion date
2021-05-31
Last updated
2023-07-14

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

Conditions

Non-Alcoholic Fatty Liver Disease, Liver Steatosis

Keywords

Empagliflozin, Dulaglutide, Liver Steatosis

Brief summary

The goal of this clinical study is to compare the therapeutic effect of Dulaglutide and Empagliflozin in patients with Diabetes Mellitus type 2 and Non-Alcoholic Fatty Liver Disease. The main question it aims to answer is: Is there a beneficial effect regarding liver steatosis in patients receiving either of these 2 medications and which is more effective? Patients will undergo shearwave elastography, magnetic resonance imaging, and ultrasound. Furthermore, calculation of the Fatty Liver Index (FLI), the Fibrosis-4 Index (FIB-4), as well as the Aspartate Aminotransferase to Platelet ratio Index (APRI) and the NAFLD Fibrosis Score (NFS) will be performed. Researchers will compare 3 groups: Group 1 will receive oral Empagliflozin, as add-on to their previous treatment regimen, for 52 weeks. Group 2 will receive subcutaneous Dulaglutide, as add-on to their previous treatment regimen, for 52 weeks. Group 3 will receive other optimal antidiabetic treatment (apart from agents of the GLP1-ras or SGLT2-is families) for 52 weeks.

Detailed description

Rationale: NAFLD is the most common chronic liver disease worldwide. Presently, relative clinical guidelines focus on weight loss through apporopriate diet and lifestyle. The Glucagon-Like Peptide 1 receptor agonists and the Sodium-Glucose Co-transporter 2 inhibitors constitute novel agents that seem to exert beneficial effects beyond glycemic control. Dulaglutide will be used from the GLP1-ras family and Empagliflozin from the SGLT2-is family. Research question: Is the use of Empagliflozin or Dulaglutide effective in improving liver fat fraction in patients with type 2 diabetes mellitus and NAFLD? Which is more beneficial? Hypothesis: The investigators hypothesize that both Dulaglutide and Empagliflozin have a role in treating patients with DM2 and NAFLD. Aim of the study: To compare the effect of Dulaglutide and Empagliflozin in liver fat fraction of diabetic patients after a year of treatment. Objectives: Assess liver steatosis change in patients. Determine percentage of those with \>30% liver fat concentration reduction. Compare Empagliflozin group with Dulaglutide group and Control group. Evaluate the impact of the medications used on glycemic control, weight loss, liver enzymes, lipids and the Fatty Liver Index (FLI), the Fibrosis-4 Index (FIB-4), as well as the Aspartate Aminotransferase to Platelet ratio Index (APRI) and the NAFLD Fibrosis Score (NFS). Material and methods: Site of study: This study will be conducted in the 2nd Department of Internal Medicine of Hippocration General Hospital, and the Therapeutic Department of General Hospital Alexandra, Athens, Greece. Type of study: This is a prospective open-label observational study. Subjects allocation: Group 1: patients will receive oral Empagliflozin, as add-on to their previous treatment regimen, for 52 weeks. Group 2: patients will receive subcutaneous Dulaglutide, as add-on to their previous treatment regimen, for 52 weeks. Group 3: patients will receive other optimal antidiabetic treatment (apart from agents of the GLP1-ras or SGLT2-is families) for 52 weeks. Patients receiving Pioglitazone were not included in the study. Steps of performance and techniques: Medical history and complete physical examination. Informed consent. Calculation of BMI, measurement of waist and hip circumference. Blood tests including: Liver function tests, Complete blood count, Urea and Creatinine, Lipid profile (total cholesterol, triglycerides, LDL, HDL), fasting plasma glucose and HbA1c. Abdominal ultrasound, Magnetic Resonance Imaging-Proton Density Fat Fraction, Shearwave Elastography. Calculation of the Fatty Liver Index (FLI), the Fibrosis-4 Index (FIB-4), as well as the Aspartate Aminotransferase to Platelet ratio Index (APRI) and the NAFLD Fibrosis Score (NFS). Assessment of changes between date of entry in the study and 52 weeks of treatment.

Interventions

DRUGEmpagliflozin

Empagliflozin 10mg daily, as add-on to previous treatment regimen.

DRUGDulaglutide

Dulaglutide 1.5mg weekly, as add-on to previous treatment regimen

Optimal anti-diabetic treatment excluding agents of the GLP1-ras or SGLT2-is families.

Sponsors

Alexandra Hospital, Athens, Greece
CollaboratorOTHER
Hippocration General Hospital
CollaboratorOTHER
National and Kapodistrian University of Athens
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
25 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Presence of diabetes mellitus type 2 and non-alcoholic fatty liver Stable anti-diabetic treatment regimen for the past 6 months

Exclusion criteria

Recent (last 5 years) medical history of cancer, pancreatitis, viral hepatitis or any other cause of liver disease (alcohol abuse, autoimmune hepatitis, hemochromatosis, heart failure etc.) Recent alteration (\<6 months) of anti-diabetic regimen. Already established treatment with GLP1-ras or SGLT2-is prior to screening. Treatment with Pioglitazone. Corticotherapy administration. Pregnant or planning for pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Liver Fat Fraction reduction52 weeksChange of Liver Fat Fraction as calculated by MRI-PDFF
>30% Liver Fat Fraction reduction52 weeksPercentage of each group's participants that achieves \>30% Liver Fat Fraction reduction

Secondary

MeasureTime frameDescription
Fatty Liver Index (FLI)52 weeksEvaluation of FLI change in each group.
Fibrosis-4 Index (FIB-4)52 weeksEvaluation of FIB-4 change in each group.
HbA1c change52 weeksEvaluation of HbA1c change in each group
NAFLD Fibrosis Score (NFS)52 weeksEvaluation of NFS change in each group.
Shearwave Elastography (SWE)52 weeksEvaluation of SWE change in each group.
Aspartate Aminotransferase to Platelet ratio Index (APRI)52 weeksEvaluation of APRI change in each group.
Body Mass Index change52 weeksEvaluation of Body Mass Index change in each group

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026