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Withdrawn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
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring heart failure, hypogonadism, testosterone
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
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
NCT ID
NCT01377103
First Posted
May 18, 2011
Last Updated
July 14, 2017
Sponsor
Cedars-Sinai Medical Center
Collaborators
Abbott
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Withdrawn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
Learn more about this trial
Testosterone Therapy in Heart Failure
We'll reach out to this number within 24 hrs