Phase 2
N=35
Effects of Aromatase Inhibition Versus Testosterone in Older Men With Low Testosterone: Randomized-Controlled Trial.
Hypogonadism · Diabetes · Sarcopenia · Osteoporosis · Depression
Bottom Line
View on ClinicalTrials.gov: NCT00104572 ↗Enrolled (actual)
35
Serious AEs
27.3%
Results posted
Mar 2016
Primary outcome: Primary: Effect of Testosterone Gel vs. Anastrozole on Bone Mineral Density — 0.042; 0.008; 0.047 g/cm2
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Androgel (Testosterone Gel) (Drug); Anastrozole (Aromatase Inhibitor) (Drug); Placebo tablet (Drug); Placebo gel (Drug); Calcium Cardone 500mg with vitamin D 400 IU (Dietary_supplement)
- Age
- Older Adult · 65+ yrs
- Sex
- Male
- Sponsor
- National Institute on Aging (NIA)
- Primary completion
- Dec 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Effect of Testosterone Gel vs. Anastrozole on Bone Mineral Density |
0.042; 0.008; 0.047 | — |
| SECONDARY Effect of Testosterone Gel vs. Anastrozole on Pulsatile Growth Hormone Release |
5.8; 10; 7.7 | — |
| SECONDARY Effect of Testosterone Gel vs. Anastrozole on Glucose Tolerance/Lipid Metabolism |
-0.05; 0.15; -0.11 | — |
| SECONDARY Effect of Testosterone Gel vs. Anastrozole on Prostate Volume/Prostate Specific Antigen Levels/Urinary Function |
4.5; -1.66; -1.05 | — |
Summary
Background: Men≥65 years often produce lower levels of testosterone, meaning there is less testosterone circulating to the tissues of the body. This is associated with negative effects on muscle strength, bone density, sexual function, mood, and the ability to think to the best of one's ability. Testosterone replacement therapy often involves injections, patches, or gels that help to raise circulating testosterone levels, but these therapies often have side effects because they lead to imbalance of other hormones. Researchers have been studying the effectiveness of anastrozole, a drug that can lower estrogen levels while simultaneously increasing testosterone levels, as a treatment for the negative effects of decreased circulating testosterone levels that occur naturally with aging. Objectives: To evaluate whether anastrozole is as effective as testosterone gel in improving bone and muscle strength, hormone levels, and brain function in men over 65 years of age. Eligibility: Healthy men at least 65 years of age who have low levels of testosterone. Design: The study involves six study visits over a total of 12 months: screening, baseline, 6 weeks, 3 months, 6 months, and 12 months. All participants will receive calcium and vitamin D supplements to take daily, and will be randomized to one of three groups:Testosterone gel and placebo tablet, Anastrozole tablet and placebo gel, Placebo tablet and gel. Participants will have the following tests at each specified visit:Screening: Blood tests and rectal ultrasound to evaluate the prostate;Baseline: Blood and urine tests; growth hormone levels, muscle strength, bone density, and balance evaluation; imaging studies; cognitive testing; and questionnaires on quality of life, sexual function, depression, and urinary symptoms;Six weeks: Blood tests and dose adjustment of the gel or tablet;Three months: Blood and urine tests; growth hormone, muscle strength, bone density, and balance evaluation; and questionnaires on quality of life, sexual function, depression, and urinary symptoms;Six months: Blood and urine tests; muscle strength, bone density, and balance evaluation; cognitive testing; and questionnaires on quality of life, sexual function, depression, and urinary symptoms;Twelve months: Blood and urine tests; rectal ultrasound; muscle strength, bone density, and balance evaluation; imaging studies; cognitive testing; and questionnaires on quality of life, sexual function, depression, and urinary symptoms.
Eligibility Criteria
- INCLUSION CRITERIA:
- Men age 65 years or older
- Serum testosterone level less than or equal to 350 ng/dl
- Subject is able to complete an informed consent
EXCLUSION CRITERIA
- History of Stroke
- History of Dementia
- History of Diabetes
- Blood pressure at rest of > 155/90 mmHg. Elevated systolic or diastolic reading renders subject ineligible
- Chronic medical condition, i.e. congestive heart failure
- Arthritis, severe enough to prevent completion of the strength testing, history of joint replacement of knees or hip.
- Inability to walk 50 meters
- Known disease of the bone and/or taking medications to treat osteoporosis, i.e.
Fosamax, Evista, Miacalcin
- History of Gastric surgery
- History of prostate cancer or any other cancers, including blood dyscrasias
- History of severe benign prostatic hyperplasia (causing urinary problems)
- History of heart attack or open-heart surgery within the past 6 months
- Use of steroids within the past 3 months, including prednisone and/or cortisone injections, and inhaled steroids. Topical steroid cream is acceptable.
- If you do not agree to refrain from taking the drugs Viagra, Cialis or Levitra for the duration of the study
- Use of anabolic steroids, i.e. testosterone, (or any analog of testosterone) Dehydroepiandrosterone or any growth promoters i.e. growth hormone itself or analogs of growth hormone
- Use of anti-androgen medications, i.e. Aldactone, Tagamet, Proscar, estrogens
- Use of Dilantin or Phenobarbital
- Alcohol intake > 30 grams (drink more than 2 beers per day OR more than 1 glass of wine or cocktail daily)
- Currently smokes any tobacco product
- Having started a new medication during the past three months which may interfere with the outcome measures of the study
- Polycythemia
- Prostate specific antigen > 4.0 ng/dl
- Hematocrit < 36
- Liver function tests greater than 2 times upper normal limits or abnormal electrolytes, calcium or Parathyroid hormone , at the discretion of the investigator
- Mini Mental Status Exam score less than or equal to 24
Data sourced from ClinicalTrials.gov (NCT00104572). 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.