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The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Levels With Coronary Artery Disease After Successful Intervention of the Blockage or Narrowed Heart Artery
This study is currently recruiting participants.
Verified by Mount Sinai School of Medicine, January 2007
Sponsors and Collaborators: Mount Sinai School of Medicine
Solvay Pharmaceuticals
Information provided by: Mount Sinai School of Medicine
ClinicalTrials.gov Identifier: NCT00413244
  Purpose

The purpose of the study is to find out if giving the study drug, Androgel (testosterone) as a testosterone replacement help bring the testosterone to an acceptable level and to find out if it will help improve heart condition in males with coronary artery disease (CAD) following successful percutaneous coronary intervention.


Condition Intervention Phase
Coronary Artery Disease
Drug: AndroGel 5 Grams
Phase III

MedlinePlus related topics: Coronary Artery Disease
Drug Information available for: Testosterone Methyltestosterone Oxymesterone Testosterone enanthate Testosterone Propionate Testosterone undecanoate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: The Cardiac Benefit of Androgen Replacement in Hypogonadal Males With Coronary Artery Disease Following Successful Percutaneous Coronary Intervention (PCI).

Further study details as provided by Mount Sinai School of Medicine:

Primary Outcome Measures:
  • objective markers of cardiac disease following successful percutaneous coronary intervention (3 months after the procedure) for coronary artery disease as measured by cardiac stress test (

Secondary Outcome Measures:
  • Improve Angina status as measured by Seattle Angina Questionnaire (SAQ)
  • Improve Endothelial function as measured PAT
  • Improve Cardiac inflammatory markers
  • Improve Metabolic syndrome-related parameters e)
  • Improve Quality of life parameters
  • Improve erectile function

Estimated Enrollment: 75
Study Start Date: January 2007
Estimated Study Completion Date: January 2008
Detailed Description:

Males with coronary heart disease have lower serum levels of bioavailable testosterone than men of a similar age with normal coronary angiograms (English, European Heart Journal, 2000). Low plasma testosterone has been associated with known risk factors for CHD, including age, obesity, hyperinsulinemia, diabetes, and adverse lipid profile.

Testosterone has also been shown in numerous studies to be a vasodilator. Recently, testosterone replacement compared with placebo, in hypogonadal men was shown to improve time to ischemic threshold, assessed by treadmill exercise testing at 4 and 12 weeks (Malkin, Heart, 2000). Prior studies had also shown a beneficial effect on exercise-induced ischemia in men with CAD, but not exclusively hypogonadal men (Jaffe,Br Heart J 1977; Rosano, Circulation, 1999; English, Circulation, 2000). In addition, this proposed study would be the first study to assess if the anti-anginal effects persists long term.

This is a randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of testosterone supplementation in hypogonadal men with coronary artery disease following successful revascularization with percutaneous coronary intervention (PCI). Only those men who had successful coronary artery revascularization, and on stable cardiac medical regimen for the prior 4 weeks will be included. Eligible patients will then be randomized on a 2:1 basis with 50 subjects receiving 5 grams of AndroGel and 25 subjects receiving placebo gel.

The men in this study who demonstrate hypogonadism represent a novel population to demonstrate the safety and efficacy of testosterone supplementation to improve cardiac function and outcomes. We hypothesize that treatment of hypogonadism in men with CAD, following successful PCI, will significantly improve cardiac ischemic threshold as assessed by cardiac stress testing. Furthermore, additional cardiac endpoints such as angina status, endothelial function and inflammatory serum markers will also demonstrate significant benefit in the testosterone treated group.

  Eligibility

Ages Eligible for Study:   40 Years to 75 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adult male patients with coronary artery disease (CAD) (one to three vessel diseased).
  • Stable cardiac status at least 3 months after percutaneous coronary intervention (PCI).
  • No change in cardiac medications for 4 weeks prior to enrollment.
  • Testosterone < 300 ng/dl
  • Sex Hormone Binding Globulin (SHBG) < 7nmol/liter and Free Testosterone < 50pg/dl
  • Prostate Specific Antigen (PSA) < 2.5 ng/mL or 2.6-3.7ng/mL with a negative prostate biopsy within the last 6 months and pathology report available for investigator’s review.
  • Subgroup of diabetics with well to moderately controlled diabetes (defined by a HgbA1c of < 9mg/dL.

Exclusion Criteria:

  • Hematocrit greater than 50%.
  • Severe hypertension (exhibit systolic blood pressure >180mmHg and diastolic blood pressure >110 mmHg at baseline visit or a have a history of malignant hypertension.
  • Significant cardiac arrhythmia (supraventricular tachycardia [SVT] or ventricular tachycardia with heart rate exceeding 110 beats per minute at Visit 1).
  • ECG abnormalities precluding ST segment analysis on treadmill, or inability to walk on treadmill.
  • Poorly controlled, symptomatic, active medical problems (HIV, hepatitis, cancer, benign prostatic hypertrophy, alcohol or drug abuse, major depressive disorder).
  • Neurological or psychiatric disorder that would compromise the patient’s ability to give informed consent or adhere to the requirements of the protocol.
  • History of prostate cancer
  • History of hypersensitivity to transdermal testosterone gel.
  • International Prostate Symptom Score (IPSS) >19 at Visit 1.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00413244

Contacts
Contact: Lourdes Campos-Grundvig, RN (212) 241-3141 Lourdes.Campos-Grundvig@msnyuhealth.org

Locations
United States, New York
Mount Sinai School of Medicine Recruiting
New York, New York, United States, 10029
Contact: Lourdes Campos-Grundvig, RN     212-241-3141     Lourdes.Campos-Grundvig@msnyuhealth.org    
Principal Investigator: Mary Ann McLaughlin, MD            
Sponsors and Collaborators
Mount Sinai School of Medicine
Solvay Pharmaceuticals
Investigators
Principal Investigator: Mary Ann McLaughlin, MD Mount Sinai School of Medcine
  More Information

Study ID Numbers: 06-1081
Study First Received: December 18, 2006
Last Updated: January 25, 2007
ClinicalTrials.gov Identifier: NCT00413244  
Health Authority: United States: Institutional Review Board

Keywords provided by Mount Sinai School of Medicine:
Hypogonadal men with coronary artery disease following successful percutaneous coronary intervention (PCI)

Study placed in the following topic categories:
Arterial Occlusive Diseases
Coronary Disease
Testosterone
Heart Diseases
Myocardial Ischemia
Vascular Diseases
Methyltestosterone
Arteriosclerosis
Ischemia
Coronary Artery Disease
Testosterone 17 beta-cypionate

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 14, 2009