Phase 2
N=22
Effects of Testosterone Gel on Carbohydrate and Lipid Metabolism In Elderly Obese Men
Aging · Obesity · Insulin Resistance · Hypogonadism
Bottom Line
View on ClinicalTrials.gov: NCT00365794 ↗Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Aug 2019
Primary outcome: Primary: Change in Total Mass and Regional Adipose Adiposiy — 0.3; -1.4; -0.9; -0.7 kilograms — p=0.77
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Topical testosterone gel 10 g/day (Drug)
- Age
- Adult, Older Adult · 60+ yrs
- Sex
- Male
- Sponsor
- University of Southern California
- Primary completion
- Dec 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Total Mass and Regional Adipose Adiposiy |
0.3; -1.4; -0.9; -0.7 | 0.77 |
| PRIMARY Change in Hepatic Lipid |
-36 | 0.12 |
| PRIMARY Intramyocellular Lipid (IMCL) |
-30 | 0.008 sig |
| SECONDARY Change in Percentage of Total Body Fat |
-1.6 | 0.0002 sig |
| SECONDARY Change in Total and Regional Carbohydrate Metabolism During a 2-hr Hyperinsulinemic Euglycemic Clamp and [6,6-2H2] Glucose Studies (Peripheral Glucose Disposal [Rd],Hepatic Glucose Output [HGO]) |
1.05; -0.16; 1.16 | 0.04 sig |
| SECONDARY Change in Skeletal Muscle Mass by DEXA |
1.2 | 0.0006 sig |
| SECONDARY Plasma Lipids |
-0.33; -0.52; -0.23; -0.10 | 0.02 sig |
| SECONDARY Change in HOMA-IR |
-0.75 | 0.06 |
| SECONDARY Change in Basal FFAs in Plasma |
-0.1 | 0.97 |
| SECONDARY Change in Plasma Free Fatty Acids During Glucose Clamp |
-0.1 | 0.83 |
Summary
A. HYPOTHESES: In older men low testosterone levels, abdominal obesity and elevated fasting insulin who are at risk for the cardiovascular complications such as heart attack and stroke.
1. Supplemental testosterone will decrease abdominal adipose tissue and hepatic fat) and appendicular fat and intramyocellular lipid in peripheral muscles (IMCL).
2. Supplemental testosterone will improve insulin sensitivity by:
1. Decreasing hepatic glucose output (HGO), a measure of central insulin resistance
2. increasing peipheral glucose disposal (Rd), a measure of periperal insuln sensiivity
3. . Improving peripheral glucose disposal (Rd) by reducing IMCL
4. Increasing appendicular skeletal muscle mass
B. OBJECTIVES:
1. Primary Objective: To determine the effects of supplemental testosterone to achieve testosterone levels in the upper normal physiologic range on central adipose tissue (abdominal and hepatic fat) and peripheral skeletal muscle fat (appendicular fat and IMCL).
2. Secondary Objectives: To determine the effects of supplemental testosterone to achieve testosterone levels in the upper normal physiologic range:on central insulin sensitivity ( hepatic glucose output ([HGO]) and peripheral insulin sensitivity (glucose disposal (Rd)
Results of this study will provide greater understanding whether androgen therapy enhances insulin sensitivity by decreasing HGO, improving peripheral Rd and if these desired effects are achieved, whether they are due to reductions in abdominal fat or liver lipid, IMCL or effects of augmenting muscle mass per se.
Results will generate hypotheses to investigate cellular and molecular mechanisms of androgen effects in persons at risk for the Metabolic Syndrome.
Eligibility Criteria
Inclusion Criteria
- Entry Criteria:
- Men > 60 years of age
- Total testosterone 102 cm
- Fasting insulin level > 18 U/L
Exclusion Criteria
- PSA > 4.1, symptoms of obstructive uropathy (AUA score > 14), unexplained prostate nodule or gland firmness
- Hematocrit > 50%
- Malignancy other than cutaneous cancers
- Sleep apnea requiring CPAP
- History of myocardial infarction, angina or stroke within the previous 6 months
- Clinical diagnosis of diabetes or FPG > 126 mg/dL
- Hypothyroidism not controlled to euthyroid levels with medication for at least 3 months
- LDL-C >160 mg/dL
- Transaminases > 1.5X ULN
- Systemic anticoagulation with warfarin
- Active progressive resistance training
- Dieting for weight loss
- Active inflammatory condition (e.g. rheumatoid arthritis)
- Use of any anabolic agent (e.g. growth hormone, testosterone precursor, anabolic steroid)or cytokine therapy in the proceeding 12 months
Data sourced from ClinicalTrials.gov (NCT00365794). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.