Effects of Aromatase Inhibition Versus Testosterone in Older Men With Low Testosterone: Randomized-Controlled Trial.
Hypogonadism, Diabetes, Sarcopenia
About this trial
This is an interventional treatment trial for Hypogonadism focused on measuring Estrogen, Glucose Tolerance, Bone Density, Quality-of-Life, Sarcopenia
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
Sites / Locations
- National Institute of Aging, Clinical Research Unit
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Placebo Comparator
(Androgel) testosterone gel
anastrozole (Aromatase inhibitor)
placebo
17 participants will receive testosterone gel (5 gm) plus placebo tablet daily for 12 months and 'Calcium Cardone 500mg with vitamin D 400 IU'
14 participants will receive anastrozole 1 mg tablet plus placebo gel daily for 12 months and 'Calcium Cardone 500mg with vitamin D 400 IU'
13 participants will receive a placebo tablet and placebo gel daily for 12 months and 'Calcium Cardone 500mg with vitamin D 400 IU'