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View Clinical Trial (Medical Research Study)
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Dose-Response of Gonadal Steroids and Bone Turnover in Men - NCT00114114-02114 (Clinical Trial 125106)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy125106.aspx
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| City: |
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Boston |
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State:
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MA |
| Zip Code: |
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02114 |
| Conditions: |
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Healthy Volunteers |
| Purpose: |
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The purpose of this study is to determine the levels of testosterone and/or estradiol at
which changes in bone turnover, body composition, strength, sexual function etc. begin to
occur. This information may help determine when to intervene with hormone replacement
therapy in aging men.
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| Study summary: |
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There are 3 arms to this protocol, each with 5 or 6 groups.
In Arm 1, 240 men age 20-50 will receive goserelin acetate (Zoladex) plus Androgel (or
placebo). (Note Arm 1 is closed to recruitment).
In Arm 2, 200 men age 20-50 will receive goserelin acetate (Zoladex) plus Androgel (or
placebo) plus anastrazole (Arimidex). (Arm 2 is recruiting).
In Arm 3, 240 men age 60 or greater will receive goserelin acetate (Zoladex) plus Androgel
(or placebo). (Arm 3 is recruiting).
For each arm, subjects will be screened on the MGH General Clinical Research Center (GCRC).
After obtaining informed consent for the screening procedures, subjects will undergo a
complete history and physical examination. If no exclusionary findings are noted during the
history and physical examination, blood will be drawn to measure hemoglobin, routine
chemistries (including serum calcium, liver function tests, and creatinine), and serum
levels of PTH, 25-OH vitamin D, TSH, T, and PSA.
Subjects who are successfully screened will be randomly assigned by a computer to one of 5
groups. All subjects will receive a GnRH agonist goserelin acetate (Zoladex; AstraZeneca,
Wilmington, DE) 3.6 mg sc every 4 weeks for 16 weeks. Subjects in Group 1 will receive
goserelin acetate and placebo for Androgel. Subjects in Groups 2-5 will receive varying
doses of Androgel. In Arms 1 and 3, a sixth group will receive double placebo (e.g. placebo
Zoladex and placebo Androgel). Subjects will be blinded with respect to group assignment.
Dietary calcium intake will be assessed by a research dietitian and adjustments made through
diet or supplements so that calcium intake is between 1000 and 1200 mg/day.
Subjects will be seen on the GCRC at 4 week intervals for 16 weeks (0, 4, 8, 12, and 16
weeks). At each visit, compliance with Androgel' will be assessed by reviewing a medication
diary. A standardized series of questions will be posed to each subject to assess potential
side effects of the study drugs. Subjects receiving Androgel' will be given a new 4 week
supply of medication (except at week 16). A fasting blood and second voided urine sample
will be collected. After the blood and urine samples have been obtained, subjects will be
given their goserelin injection. The blood and urine tests listed below as well as
anthropometric measures, and questionnaires will be performed at each visit. DXA, CT scans,
and strength assessments will be performed at 0 and 16 weeks only. Subjects who discontinue
participation at or after week 8 will be asked if they are willing to have an early
discontinuation visit in which all procedures normally done at week 16 will be performed.
The following measures will be assessed:
- Routine chemistries and PSA (for safety assessment)
- Bone turnover using blood and urine tests
- Hormones
- Lipids
- Body composition
- Strength
- Symptoms of hypogonadism |
| Criteria: |
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Inclusion Criteria:
- Healthy men age 20 to 50 years or 60 years and older
Exclusion Criteria:
- History of significant cardiac, renal, pulmonary, hepatic, benign prostatic
hyperplasia, or malignant disease, current alcohol or illicit drug abuse, or major
psychiatric disorders.
- Current diagnoses of disorders known to affect bone metabolism including
hyperthyroidism, hyperparathyroidism, osteomalacia, or Paget's disease.
- Current use of medications known to affect bone metabolism including estrogens,
androgens, anti-estrogens, bisphosphonates, calcitonin, fluoride, oral or inhaled
glucocorticoids, suppressive doses of thyroxine, lithium, pharmacological doses of
vitamin D (greater than 2000 IU/day), or anti-convulsants.
- Cognitive or intellectual impairment that precludes complete understanding of the
study protocol.
- History of deep vein thrombosis, pulmonary embolism, or clotting disorders.
- Serum 25-OH vitamin D < 15 ng/mL
- Serum PTH < 10 or > 65 pg/mL
- Serum TSH < 0.5 or > 5.0 U/L
- Serum calcium > 10.6 mg/dL
- Serum creatinine > 2 mg/dL
- Serum AST or ALT > 2x the upper limit of normal
- Serum bilirubin > 2 mg/dL
- Serum alkaline phosphatase > 150 U/L
- Plasma hemoglobin < 11 gm/dL.
- Fracture within the last 6 months.
- Serum testosterone level < 270 or > 1070 ng/dL
- Serum PSA level > 4 ug/L.
- International Prostate Symptom Score (IPSS) > 19 |
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| Study is available at: |
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Massachusetts General Hospital
Boston, MA 02114
United States
Primary Contact:
JOEL S. FINKELSTEIN, MD
Email: jfinkelstein@partners.org
Phone: 617-726-6723
Secondary Contact:
JOEL S. FINKELSTEIN, MD
Email: jfinkelstein@partners.org
Phone: 617-726-6723 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 15, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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