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Effects of Aromatase Inhibition Versus Testosterone in Older Men With Low Testosterone: Randomized-Controlled Trial.

Primary Purpose

Hypogonadism, Diabetes, Sarcopenia

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Androgel (Testosterone Gel)
Anastrozole (Aromatase Inhibitor)
Placebo tablet
Placebo gel
Calcium Cardone 500mg with vitamin D 400 IU
Sponsored by
National Institute on Aging (NIA)
About
Eligibility
Locations
Arms
Outcomes
Full info

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

65 Years - undefined (Older Adult)MaleAccepts Healthy Volunteers

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

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

(Androgel) testosterone gel

anastrozole (Aromatase inhibitor)

placebo

Arm Description

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'

Outcomes

Primary Outcome Measures

Effect of Testosterone Gel vs. Anastrozole on Bone Mineral Density
bone mineral density lumbar spine for all arms testosterone gel, anastrozole and placebo

Secondary Outcome Measures

Effect of Testosterone Gel vs. Anastrozole on Pulsatile Growth Hormone Release
Overnight Growth hormone measures (total hormone secretion) for groups testosterone gel, anastrozole and placebo
Effect of Testosterone Gel vs. Anastrozole on Glucose Tolerance/Lipid Metabolism
Primary outcome HOMA-IR for all groups testosterone gel, anastrozole and placebo Insulin resistance measure by HOMA-IR is a score if a person is insulin resistance the score should be between minimum 0.7- maximum 2 or more. Absolute changes in HOMAIR in all treatment arms, calculation time frame 1 year minus baseline point.
Effect of Testosterone Gel vs. Anastrozole on Prostate Volume/Prostate Specific Antigen Levels/Urinary Function
rectal ultrasound prostate volume for all groups testosterone gel, anastrozole and placebo. Absolute changes in prostate volume in all treatment arms, calculation time frame 1 year minus baseline point.

Full Information

First Posted
March 1, 2005
Last Updated
October 11, 2018
Sponsor
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT00104572
Brief Title
Effects of Aromatase Inhibition Versus Testosterone in Older Men With Low Testosterone: Randomized-Controlled Trial.
Official Title
The Effects of Aromatase Inhibition and Testosterone Replacement in Sex Steroids, Pituitary Hormones, Markers of Bone Turnover, Muscle Strength, and Cognition in Older Men
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
January 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute on Aging (NIA)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
Approximately 20% of men over the age of 70 have low testosterone levels. In some studies, testosterone replacement has resulted in improvement in bone mass, muscle strength, quality of life and memory function. In the body, testosterone is converted into estrogen. Hence, it is unclear whether these beneficial effects are due to testosterone or estrogen. Research has shown that inhibition of estrogen production in men results in an increase in testosterone levels. In this study, patients will be assigned to one of three groups: one group will receive testosterone gel and a placebo tablet, one group will receive a 1mg Anastrozole tablet and a placebo gel, and one group will receive a placebo tablet and placebo gel. Each group will receive a daily dose of calcium with vitamin D. The study requires 6 visits over a 12-month period for testing and evaluation. Two of the 6 visits will require an overnight stay in the hospital so that an intravenous (IV) line can be placed in the arm to allow samples to be drawn throughout the night. Testing will include a cardiac stress test, a glucose tolerance test, bone and muscle tests, evaluation of memory function, etc. For the safety of the prostate, we will perform a prostate ultrasound at the start and end of the study and we will monitor urinary symptoms, prostate specific antigen (PSA) levels and the prostate exam throughout the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypogonadism, Diabetes, Sarcopenia, Osteoporosis, Depression
Keywords
Estrogen, Glucose Tolerance, Bone Density, Quality-of-Life, Sarcopenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
(Androgel) testosterone gel
Arm Type
Experimental
Arm Description
17 participants will receive testosterone gel (5 gm) plus placebo tablet daily for 12 months and 'Calcium Cardone 500mg with vitamin D 400 IU'
Arm Title
anastrozole (Aromatase inhibitor)
Arm Type
Experimental
Arm Description
14 participants will receive anastrozole 1 mg tablet plus placebo gel daily for 12 months and 'Calcium Cardone 500mg with vitamin D 400 IU'
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
13 participants will receive a placebo tablet and placebo gel daily for 12 months and 'Calcium Cardone 500mg with vitamin D 400 IU'
Intervention Type
Drug
Intervention Name(s)
Androgel (Testosterone Gel)
Intervention Description
1 mg tablet for 12 months
Intervention Type
Drug
Intervention Name(s)
Anastrozole (Aromatase Inhibitor)
Intervention Type
Drug
Intervention Name(s)
Placebo tablet
Intervention Description
Daily for 12 months
Intervention Type
Drug
Intervention Name(s)
Placebo gel
Intervention Description
Daily for 12 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Calcium Cardone 500mg with vitamin D 400 IU
Intervention Description
1 tablet three times a day
Primary Outcome Measure Information:
Title
Effect of Testosterone Gel vs. Anastrozole on Bone Mineral Density
Description
bone mineral density lumbar spine for all arms testosterone gel, anastrozole and placebo
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Effect of Testosterone Gel vs. Anastrozole on Pulsatile Growth Hormone Release
Description
Overnight Growth hormone measures (total hormone secretion) for groups testosterone gel, anastrozole and placebo
Time Frame
1 year
Title
Effect of Testosterone Gel vs. Anastrozole on Glucose Tolerance/Lipid Metabolism
Description
Primary outcome HOMA-IR for all groups testosterone gel, anastrozole and placebo Insulin resistance measure by HOMA-IR is a score if a person is insulin resistance the score should be between minimum 0.7- maximum 2 or more. Absolute changes in HOMAIR in all treatment arms, calculation time frame 1 year minus baseline point.
Time Frame
1 year
Title
Effect of Testosterone Gel vs. Anastrozole on Prostate Volume/Prostate Specific Antigen Levels/Urinary Function
Description
rectal ultrasound prostate volume for all groups testosterone gel, anastrozole and placebo. Absolute changes in prostate volume in all treatment arms, calculation time frame 1 year minus baseline point.
Time Frame
1 year

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Josephine M Egan, M.D.
Organizational Affiliation
National Institute on Aging (NIA)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institute of Aging, Clinical Research Unit
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
4290227
Citation
Jeffcoate SL, Brooks RV, Lim NY, London DR, Prunty FT, Spathis GS. Androgen production in hypogonadal men. J Endocrinol. 1967 Apr;37(4):401-11. doi: 10.1677/joe.0.0370401. No abstract available.
Results Reference
background
PubMed Identifier
7486793
Citation
Wheeler MJ. The determination of bio-available testosterone. Ann Clin Biochem. 1995 Jul;32 ( Pt 4):345-57. doi: 10.1177/000456329503200401. No abstract available.
Results Reference
background
PubMed Identifier
1719016
Citation
Gray A, Feldman HA, McKinlay JB, Longcope C. Age, disease, and changing sex hormone levels in middle-aged men: results of the Massachusetts Male Aging Study. J Clin Endocrinol Metab. 1991 Nov;73(5):1016-25. doi: 10.1210/jcem-73-5-1016.
Results Reference
background
PubMed Identifier
26950683
Citation
Dias JP, Melvin D, Shardell M, Ferrucci L, Chia CW, Gharib M, Egan JM, Basaria S. Effects of Transdermal Testosterone Gel or an Aromatase Inhibitor on Prostate Volume in Older Men. J Clin Endocrinol Metab. 2016 Apr;101(4):1865-71. doi: 10.1210/jc.2016-1111. Epub 2016 Mar 7.
Results Reference
derived

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Effects of Aromatase Inhibition Versus Testosterone in Older Men With Low Testosterone: Randomized-Controlled Trial.

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