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Study to Determine the Effects of Testosterone Replacement Therapy in Aging Men with Androgen Deficiency - Article


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Testosterone Injection

Delatestryl; Depo-Testosterone



Clinical Trial: Study to Determine the Effects of Testosterone Replacement Therapy in Aging Men with Androgen Deficiency

This study has been completed.

Sponsors and Collaborators: Urological Sciences Research Foundation
Solvay Pharmaceuticals, Inc.
Watson Pharmaceuticals
Information provided by: Urological Sciences Research Foundation
ClinicalTrials.gov Identifier: NCT00161304

Purpose

The T-001 study is a placebo-controlled investigation of the effects of injectable testosterone replacement therapy on prostate tissues of aging men with low testosterone levels. The primary objectives of the study are to measure the changes in tissue hormones and other biomarkers in the prostate tissue specimens.
Condition Intervention Phase
Men with low testosterone levels
 Drug: Testosterone Enanthate
Phase II
Phase III

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: Effects of Testosterone Administration on Tissues of Men with A.D.A.M. (Androgen Deficiency of Aging Men)

Further Study Details: 

Expected Total Enrollment:  44

Study start: April 2003;  Study completion: November 2004
Last follow-up: November 2004;  Data entry closure: November 2004

Eligibility

Ages Eligible for Study:  50 Years and above,  Genders Eligible for Study:  Male

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:Inclusion Criteria

  1. Male aged 50-80 years of age, ambulatory, and in good general physical and mental health.
  2. Clinical diagnosis of hypogonadism defined as a serum testosterone level less than 300 ng/dl on a morning serum sample during the screening period.
  3. Answering yes to question 1 or 7 or to any three questions total on the Morley index at baseline.
  4. PSA <10 ng/ml
  5. Subject is able to give informed consent.

Exclusion Criteria

  1. Failure to meet the criteria for inclusion
  2. History of allergy to testosterone or any components of the delivery system.
  3. Significant abnormalities on pre-study clinical examination or laboratory measurements.
  4. Treatment with any investigational drug during the previous month.
  5. Drug or alcohol abuse or dependence.
  6. Concurrent use of testosterone and or any hormonal therapy, including health food supplements and herbal products, that could alter serum testosterone levels or affect the prostate (e.g. gonadotropic releasing hormone agonists, testosterone antagonists, anabolic steroids, DHEA, androstenedione, PC-SPES, chrysin and tribulus terrestris,). Use of alpha-reductase inhibitors or prostate phytotherapy within the past 3 months.
  7. Use of antidepressant medications, oral glucocorticoids, or opioids.
  8. PSA > 10 ng/ml and/or prostate biopsy positive for cancer at screening. Any patient in whom there is a suspicion of prostate cancer must undergo appropriate testing to rule out cancer prior to entry into the study.
  9. IPSS score  20.
  10. History of malignancy of any type (except basal cell carcinoma).
  11. Patients with uncontrolled diabetes.
  12. Patients with known or suspected bleeding disorder. Concurrent use of Coumadin and other anticoagulants at the time of biopsy or if discontinuation of such therapy prior to biopsy poses a risk to the patient.
  13. Inability of the patient to provide written informed consent for any reason, including legal incompetence, language or comprehension difficulty, and psychological, psychiatric or emotional factors.
  14. Inability of the patient to have transrectal ultrasonography with biopsy (for any reason).
  15. A history of any illness or condition that, in the opinion of the investigator, might confound the results of the study or pose additional risk to the patient.

Location Information


California
      Urological Sciences Research Foundation, Culver City,  California,  90232,  United States

Study chairs or principal investigators

Leonard S Marks, M.D.,  Principal Investigator,  Urological Sciences Research Foundation   

More Information

Study ID Numbers:  T-001
Last Updated:  September 11, 2005
Record first received:  September 8, 2005
ClinicalTrials.gov Identifier:  NCT00161304
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-13

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Page Updated: June 1, 2005
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