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Testosterone Effects on Men With the Metabolic Syndrome

Primary Purpose

Metabolic Syndrome

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Testosterone
Anastrozole
Goserelin
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome focused on measuring Testosterone, Insulin resistance, Insulin sensitivity, Metabolic disorders

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 50-75 yr
  2. Diagnosis of the metabolic syndrome defined by the American Heart Association/National Heart, Lung, and Blood Institute guidelines as the presence of three or more of the following:

    • Waist circumference > 102 cm
    • Serum triglycerides > 150 mg/dL
    • HDL cholesterol < 40 mg/dL
    • Blood pressure > 130 mm Hg systolic or 85 mm Hg diastolic, or treatment with anti-hypertensives
    • Fasting serum glucose > 100 mg/dL
  3. Plasma total testosterone level less than 300 ng/dL (1 SD below the mean for young healthy men)
  4. Stable weight for previous three months (no weight change greater than or equal to +/-10 lbs)
  5. Normal TSH, prolactin and prostate specific antigen (PSA) levels (<2.5 ng/mL)

Exclusion Criteria:

  1. New diagnosis of type 2 diabetes as defined by the ADA criteria: fasting glucose greater than 126 mg/dL or random blood glucose greater than 200 mg/dL on two occasions, or on oral hypoglycemic agents
  2. History of testicular disorders (i.e. cryptorchidism)
  3. History of bleeding disorders (i.e. thrombocytopenia) or baseline hemoglobin levels less than 12g/dL
  4. History of prostate cancer
  5. History of sleep apnea (subjects will also be excluded if at their baseline assessment they admit to heavy snoring, restless sleep, and/or excessive daytime somnolence)
  6. Symptoms of urinary outflow obstruction (i.e. benign prostatic hypertrophy)
  7. Illicit drug use or heavy alcohol use (>4 drinks/day)
  8. Allergic disorders
  9. Current medications (must exclude individuals taking the following medications: Testosterone, Cimetidine, Spironolactone, Ketoconazole, Finasteride, DHEA, Androstenedione, Oral steroids, GnRH analogs)

Sites / Locations

    Outcomes

    Primary Outcome Measures

    insulin sensitivity
    muscle and body fat distribution
    VO2 max
    resting metabolic rate
    muscle biopsy analysis

    Secondary Outcome Measures

    Full Information

    First Posted
    September 26, 2006
    Last Updated
    December 4, 2008
    Sponsor
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00382057
    Brief Title
    Testosterone Effects on Men With the Metabolic Syndrome
    Official Title
    Effect of Increasing Testosterone Levels on Insulin Sensitivity in Men With the Metabolic Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2008
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    May 2006 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    March 2011 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    4. Oversight

    5. Study Description

    Brief Summary
    The metabolic syndrome is a medical condition defined by high levels of cholesterol in the blood, high blood pressure, central obesity (gain in fat around the region of the stomach), and insulin resistance (body responds less well to insulin). This state of impaired insulin resistance can lead to type 2 diabetes mellitus, which is one of the most common metabolic disorders in the U.S. Numerous studies have shown an inverse relationship between insulin resistance and testosterone levels in men, however, causality has not been established. This protocol investigates the role of testosterone in modulating insulin sensitivity in insulin resistant states such as the metabolic syndrome. The hypothesis is that testosterone administration will improve insulin sensitivity.
    Detailed Description
    This protocol will address the impact of three months of testosterone (T) therapy on all components of the metabolic syndrome and the mechanism underlying changes in insulin sensitivity by analyzing changes in body composition, and detailed studies of fat metabolism and skeletal muscle. In addition, this protocol will address the role of estradiol (E2) in mediating the effect of testosterone on insulin sensitivity. Seventy-two subjects will undergo a screening visit to assess eligibility after which a baseline evaluation will be performed. The baseline metabolic assessment will consist of an intravenous glucose tolerance test (IVGTT) to measure insulin sensitivity, MRI and DEXA scan to assess muscle and body fat distribution, VO2 max test and resting metabolic rate, and a muscle biopsy to look at how the muscle is affected by insulin and testosterone. Subjects will then be randomized to one of three 12-week treatment arms, 1) Group 1 (Placebo); 2) Group 2 (Depot GnRH agonist (Zoladex) + T + placebo); or 3) Group 3 (Zoladex + T + aromatase inhibitor (anastrozole)). The rationale for this study design is as follows. Under normal physiological conditions, administration of T leads to a concomitant increase in E2 levels due to endogenous conversion by the aromatase enzyme system. Therefore, in order to dissect the relative roles of T and E2 on insulin sensitivity, one group of subjects will receive T in conjunction with the aromatase inhibitor, anastrozole. At 13 weeks, the entire baseline evaluation including IVGTT, resting metabolic rate and VO2 max, body composition assessment by DEXA and MRI, and muscle biopsy will be repeated. Subjects will return for a follow up visit four weeks later to measure CBC, T and PSA levels, to ensure levels are within the normal range.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Metabolic Syndrome
    Keywords
    Testosterone, Insulin resistance, Insulin sensitivity, Metabolic disorders

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    72 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Testosterone
    Intervention Type
    Drug
    Intervention Name(s)
    Anastrozole
    Intervention Type
    Drug
    Intervention Name(s)
    Goserelin
    Primary Outcome Measure Information:
    Title
    insulin sensitivity
    Title
    muscle and body fat distribution
    Title
    VO2 max
    Title
    resting metabolic rate
    Title
    muscle biopsy analysis

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    50 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 50-75 yr Diagnosis of the metabolic syndrome defined by the American Heart Association/National Heart, Lung, and Blood Institute guidelines as the presence of three or more of the following: Waist circumference > 102 cm Serum triglycerides > 150 mg/dL HDL cholesterol < 40 mg/dL Blood pressure > 130 mm Hg systolic or 85 mm Hg diastolic, or treatment with anti-hypertensives Fasting serum glucose > 100 mg/dL Plasma total testosterone level less than 300 ng/dL (1 SD below the mean for young healthy men) Stable weight for previous three months (no weight change greater than or equal to +/-10 lbs) Normal TSH, prolactin and prostate specific antigen (PSA) levels (<2.5 ng/mL) Exclusion Criteria: New diagnosis of type 2 diabetes as defined by the ADA criteria: fasting glucose greater than 126 mg/dL or random blood glucose greater than 200 mg/dL on two occasions, or on oral hypoglycemic agents History of testicular disorders (i.e. cryptorchidism) History of bleeding disorders (i.e. thrombocytopenia) or baseline hemoglobin levels less than 12g/dL History of prostate cancer History of sleep apnea (subjects will also be excluded if at their baseline assessment they admit to heavy snoring, restless sleep, and/or excessive daytime somnolence) Symptoms of urinary outflow obstruction (i.e. benign prostatic hypertrophy) Illicit drug use or heavy alcohol use (>4 drinks/day) Allergic disorders Current medications (must exclude individuals taking the following medications: Testosterone, Cimetidine, Spironolactone, Ketoconazole, Finasteride, DHEA, Androstenedione, Oral steroids, GnRH analogs)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    William F Crowley, MD
    Organizational Affiliation
    Massachusetts General Hospital
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Frances J Hayes, MD
    Organizational Affiliation
    Massachusetts General Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Testosterone Effects on Men With the Metabolic Syndrome

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