Central Military Hospital
Prague, 16902, Czechia
NCT Number: NCT06519448
The goal of this clinical trial is to learn if empagliflozin works to treat non-alcoholic steatohepatitis in adults. The objectives are:
Primary Objective To evaluate the change in histological grading and staging of NASH in patients with confirmed non-alcoholic steatohepatitis (NASH) treated with empagliflozin for a duration of 48 weeks.
Secondary Objective To evaluate the change in findings from non-invasive liver elasticity measurements, laboratory tests, and anthropometric assessments after 48 weeks of empagliflozin administration.
Participants will:
Take empagliflozin every day for 12 months. Visit the clinic according to a protocol at weeks: 1, 2, 4, 12, 24, 36, 48 Visits includes checkups and tests (blood count, basic biochemistry, glycosylated hemoglobin, anthropometry, non-invasive liver stiffness measurement).
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Not applicable
Prague, 16902, Czechia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Use of empagliflozin 10 mg daily for 12 months.
Time frame: 12 months
Non-alcoholic Fatty Liver Disease Activity Score (NAS) change after intervention. The NAS can range from 0 to 8 and is calculated by the sum of scores of steatosis (0-3), lobular inflammation (0-3) and hepatocyte ballooning (0-2). In patients with NAFLD, NAS score of ≥ 5 strongly correlated with a diagnosis of "definite NASH" whereas NAS ≤ 3 correlated with a diagnosis of "not NASH".
Time frame: 12 months
Liver stiffness measured in kilopascals (kPa) by transient elastography at baseline and after intervention.
Time frame: 12 months
Continuous attenuation parameter measured in decibels per meter (dB/m) at baseline and after intervention.
Time frame: 12 months
Measurement of body weight measured in kilograms (kg) and change from baseline.
Time frame: 12 months
Measurement of body height measured in metres (m) to calculate Body Mass Index (BMI).
Time frame: 12 months
Change in BMI from baseline (measured in kg/m^2).
Time frame: 12 months
Change in activity liver functional tests (LFT) all measured in microkatals per liter (ucat/L) from baseline.
These tests comprise:
Alanine transaminase (ALT) Aspartate transaminase (AST) Gamma-glutamyl transferase (GGT) Alkaline phosphatase (ALP)
Time frame: 12 months
Change in activity concentration of bilirubin measured in micromoles per liter (umol/L) from baseline.
Time frame: 12 months
Change in cholesterol, LDL cholesterol, HDL cholesterol, triglycerides (measured in mmol/L) from baseline.
Military University Hospital, Prague
Other
Reducing Non-Alcoholic Steatohepatitis Study
Acronym: RedNASH
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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