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Testosterone Therapy in Heart Failure

Primary Purpose

Heart Failure, Hypogonadism

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
testerone gel
Placebo
Sponsored by
Cedars-Sinai Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring heart failure, hypogonadism, testosterone

Eligibility Criteria

36 Years - 79 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • male
  • NYHA class II-IV Heart Failure
  • age > 35 < 80
  • total testosterone level of <5 ng/ml

Exclusion Criteria:

  • elevated prostate specific antigen
  • elevated total or free testosterone level
  • prostate cancer or evidence of symptomatic prostatism
  • untreated prolactinemia or history of breast cancer

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Active Comparator

    Arm Label

    Placebo

    Testosterone Supplementation

    Arm Description

    Placebo Gel

    Testosterone Gel

    Outcomes

    Primary Outcome Measures

    heart failure outcomes
    rehospitalization rates, mortality, New York Heart Association class and symptomatolgy
    depression and mood
    Beck Depression Inventory: a 21-question multiple-choice self-report inventory for measuring the severity of depression
    quality of life
    Minnesota Living with Heart Failure Questionnaire

    Secondary Outcome Measures

    overall satisfaction
    Minnesota Living with Heart Failure Questionnaire
    compliance
    documentation of study medication usage
    markers for heart failure
    natriuretic peptide, creatinine, and left ventricular ejection fraction.

    Full Information

    First Posted
    May 18, 2011
    Last Updated
    July 14, 2017
    Sponsor
    Cedars-Sinai Medical Center
    Collaborators
    Abbott
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01377103
    Brief Title
    Testosterone Therapy in Heart Failure
    Official Title
    Cardiovascular and Functional Effects of Testosterone Therapy for Hypogonadal Patients With Heart Failure
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2011
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    July 2011 (undefined)
    Primary Completion Date
    October 2012 (Anticipated)
    Study Completion Date
    December 2012 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cedars-Sinai Medical Center
    Collaborators
    Abbott

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to evaluate whether benefits of topical testosterone on symptoms and function of male HF patients, and its effects on rehospitalization rates and quality of life.
    Detailed Description
    Recent evidence has started to emerge regarding the benefits of testosterone in the heart failure (HF) population. Firstly, testosterone directly augments vascular resistance by causing vasodilation of peripheral vessels which can decrease afterload and improve cardiac output. In addition, testosterone causes coronary artery vasodilation and improves cardiac ischemic threshold based on subjective and objective measures. Clinically, several studies have pointed out the potential benefits patients with HF can derive from testosterone therapy. Measures of cardiopulmonary function tests, six minute walk test, incremental shuttle walk test and baroreflex sensitivity, all of which have prognostic implications for patients with HF, show improvement with the addition of testosterone therapy to traditional-medical management. In addition to these objective measurements, mood, NYHA functional class and muscle strength are all improved by treatment with testosterone supplementation. While past studies have used functional and prognostic measures as outcomes, other issues common in patients with HF, such as sexual dysfunction and repeat hospitalizations, have the potential for improvement with testosterone therapy The majority of studies performed in the past have utilized intramuscular or transdermal patch delivery systems of testosterone as a means for supplementation. These methods have inherent issues as a means of treatment as patients often times do not have the means to receive intramuscular injections and patches have a high level of skin reactions making compliance difficult. Topical administration of testosterone gel may prove to be a more efficacious method for testosterone supplementation with a lower side effect profile and adequate absorption. It has been used with success by the general public for treatment of hypogonadal symptoms, but has not been studied in the HF population. With the emergence of studies showing promising benefits of testosterone supplementation in the HF population, the ease of topical administration for this population would provide benefits to millions suffering from HF. The investigators study aims to find the benefits of topical testosterone on symptoms and function of HF patients, and its effects on rehospitalization rates and quality of life.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Heart Failure, Hypogonadism
    Keywords
    heart failure, hypogonadism, testosterone

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo Gel
    Arm Title
    Testosterone Supplementation
    Arm Type
    Active Comparator
    Arm Description
    Testosterone Gel
    Intervention Type
    Drug
    Intervention Name(s)
    testerone gel
    Other Intervention Name(s)
    AndroGel(R)
    Intervention Description
    5g daily for 4 weeks then 7.5 or 10g daily for 8 weeks; transdermal testosterone gel
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Primary Outcome Measure Information:
    Title
    heart failure outcomes
    Description
    rehospitalization rates, mortality, New York Heart Association class and symptomatolgy
    Time Frame
    16 months
    Title
    depression and mood
    Description
    Beck Depression Inventory: a 21-question multiple-choice self-report inventory for measuring the severity of depression
    Time Frame
    16 months
    Title
    quality of life
    Description
    Minnesota Living with Heart Failure Questionnaire
    Time Frame
    16 months
    Secondary Outcome Measure Information:
    Title
    overall satisfaction
    Description
    Minnesota Living with Heart Failure Questionnaire
    Time Frame
    16 months
    Title
    compliance
    Description
    documentation of study medication usage
    Time Frame
    16 months
    Title
    markers for heart failure
    Description
    natriuretic peptide, creatinine, and left ventricular ejection fraction.
    Time Frame
    16 months

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    36 Years
    Maximum Age & Unit of Time
    79 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: male NYHA class II-IV Heart Failure age > 35 < 80 total testosterone level of <5 ng/ml Exclusion Criteria: elevated prostate specific antigen elevated total or free testosterone level prostate cancer or evidence of symptomatic prostatism untreated prolactinemia or history of breast cancer
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ernst Schwarz, MD, PhD
    Organizational Affiliation
    Cedars-Sinai Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Testosterone Therapy in Heart Failure

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