52 Week RCT to Investigate the Effect of Testosterone Undecanoate vs Placebo on Intrahepatic Fat Content in Obese/Overweight Men With T2DM/Prediabetes and Hypogonadism and Subsequent 108 Week Open Label Phase to Investigate Effects on Cardiometabolic Parameters

Who is this study for? Men with obesity or who are overweight with T2DM/prediabetes and hypogonadism
What treatments are being studied? Testosterone Undecanoate
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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
Participation Requirements
Sex: Male
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• prediabetes/T2DM

• male sex

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

• Age \>=18 -75 years

• BMI\>=25kg/m²

• Hypogonadism assessed by laboratory testing (testosterone \< 4,04ng/ml (=14nmol/l) Metformin 8 weeks stable dose, SGLT2 inhibitors 3 months stable dose, DPP4 inhibitors 3 months stable dose, GLP1 RA 3 months stable dose and long acting insulin (basal insulin) 8 weeks stable dose

• able and willing to not change diet and physical activity during enrollment in study

• consent and able to give informed consent.

Locations
Other Locations
Austria
Abt. für Endokrinologie & Stoffwechsel, Univ. Klin f. Innere Medizin III
RECRUITING
Wien
Contact Information
Primary
Jürgen Harreiter, PhD
juergen.harreiter@meduniwien.ac.at
+43 1 40400
Time Frame
Start Date: 2022-01-25
Estimated Completion Date: 2028-12
Participants
Target number of participants: 32
Treatments
Active_comparator: Testosterone undecanoate
intramuscular Testosterone undecanoate 1000mg/4ml
Placebo_comparator: Testosterone like Placebo
intramuscular Testosterone undecanoate like Placebo
Sponsors
Collaborators: Bayer
Leads: Alexandra Kautzky-Willer

This content was sourced from clinicaltrials.gov