Effects of Testosterone Undecanoate vs Placebo on Intrahepatic Fat Content in Overweight/Obese Men With T2DM or Prediabetes and Hypogonadism

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexMale
Age18-75
SponsorAlexandra Kautzky-Willer

About this trial

The epidemics of obesity, MeTSy, T2DM and CVD are increasing worldwide. Non-alcoholic fatty liver disease (NAFLD) is becoming recognized as a condition possibly involved in the pathogenesis of these diseases. The prevailing hypothesis for NAFLD pathogenesis is the 'two-hit' model, with insulin resistance and hyperinsulinemia playing essential roles, which have a plethora of effects on hepatic lipid metabolism and can lead to accumulation of triglycerides in hepatocytes. Accepted treatment for NAFLD is lifestyle modifications. Sex hormones might be relevant in T2DM development and treatment. Low testosterone (T) has deteriorating effects on glucose levels, and aggravates in obesity as aromatization of T is enhanced. T deficiency is related to increases of visceral fat accumulation and associated with development of NAFLD. T replacement might be a successful way in hypogonadism to treat obesity and counteract progression of MEtSy,T2DM or CVD driven by visceral fat accumulation or NAFLD.

Primary Objective To investigate the effects on hepatic lipid content reduction of a therapy with Testosterone undecanoate 1000mg compared to placebo given for 52 weeks in patients with type 2 diabetes mellitus and hypogonadism.

Eligibility criteria

Qualifiers

prediabetes/T2DM

male sex

HbA1c >=5.7% -9.0% or fasting glucose >=100mg/dl or postprandial glucose>= 140mg/dl

Age >=18 -75 years

Disqualifiers

Current testosterone treatment or testosterone replacement within the last 12 month

Serum creatinine>1,5mg/dl

Liver enzymes above 3 fold normal range

PSA>4.0μg/l

Trial design

Treatments tested in this trial

  • Testosterone Undecanoate
  • Placebo

Treatment groups

32 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Alexandra Kautzky-Willer

Lead sponsor

Medical University of Vienna

Sponsor institution

Bayer

Collaborator