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Effects of Testosterone and Fat Utilization

Testosterone Effects on Systemic Lipolysis and Whole Body Lipid Utilization

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03289559
Enrollment
13
Registered
2017-09-21
Start date
2006-01-01
Completion date
2014-01-01
Last updated
2017-09-21

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

Conditions

Healthy, Volunteers

Brief summary

Evidence is accumulating that there are sex differences in energy and substrate metabolism. The positive or negative consequences of such metabolic differences between men and women need to be evaluated with respect to health outcomes. The importance of aberrant lipid metabolism in metabolic diseases such as obesity, diabetes and cardiovascular disease, makes understanding the distinction between normal vs aberrant critical to future treatment and prevention strategies. Sex differences in the effects of catecholamines on lipid metabolism and substrate oxidation in non-obese, healthy individuals, have been consistently observed. In addition, distinct differences in men and women exist in the distribution of body fat, with men typically having greater central adiposity than women. Accumulation of fat in the abdomen is associated with an increased risk for metabolic abnormalities such as hyperlipidemia and insulin resistance. In the current study, therefore, the role of testosterone in determining the sex differences in catecholamine mediated substrate metabolism and deposition of dietary fat into upper versus lower body adipose tissue depots will be addressed.

Interventions

DRUGGnRH antagonist
DRUGTestosterone gel

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* normal weight (BMI of 23-29.9 kg/m2) * not be highly trained (\< 5hrs of moderate intensity, planned exercise per week).

Exclusion criteria

* Patients will be excluded if they have one or more of the following out-of-range values measured on a fasting blood sample: * glucose \<65 or \> 110 mg/dl, * insulin \> 20 uU/ml, * thyroid stimulating hormone \<0.5 or \>5.0 uU/ml, * growth hormone \>2.5 ng/ml. * Subjects who may be: * anemic (hemoglobin \< 14.5 g/dl men ), * have abnormal liver function tests: * alanine amino transferase \> 47 U/l, * aspartate aminotransferase, \> 47 U/l, * alkaline phosphatase \<39 or \>117 U/l) or * creatinine (\<0.6 or \>1.1 mg/dl).

Design outcomes

Primary

MeasureTime frameDescription
Dietary fat tracer for storage of meal derived fatty acids4 weeks50 uCi of \[1-14C\] oleic acid administered with an inpatient test meal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026