H-36731: Finasteride in Management of Elevated Red Blood Cells

Withdrawn before enrolling · Phase 3

Conditions studied: ERYTHROCYTOSIS

In brief

Hypogonadism (low testosterone) is becoming an increasingly recognized problem that affects numerous men in the United States. Symptoms may be always feeling tired, lower sex drive, and loss of muscle mass. Treatment typically involves testosterone in either injections or a topical gel form. However, administration of testosterone is not without side effects of its own. Testosterone supplementation therapy is known to cause a variety of side effects including high blood pressure and high lipids (fats) and an increased proportion of red blood cells. Side effects of increased red blood cells can include an increased risk of developing a blood clot. The increase in the red blood cells is related to dihydrotestosterone (DHT - a male sex hormone) activity. It is normal for the testosterone to become DHT. DHT has various effects on the body including growth of the prostate gland, baldness, and others and DHT levels have been linked to elevated red blood cell counts in men on testosterone. Finasteride is an FDA approved medication used in the treatment of benign prostatic hypertrophy (BPH) in men with enlarged prostate to improve symptoms and to reduce the risk of the need for surgery. Finasteride may prevent elevations in or reduce elevated red blood cell levels in men on testosterone.

Key facts

Study ID

NCT02548117

Run by

Baylor College of Medicine

People needed

0

Starts

2016-02-01

Expected to finish

2016-02-01

Last updated by the study team

2019-12-16

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Adult males 18 years of age or older
• Currently is being treated for hypogonadism with testosterone therapy using injectable testosterone.
• Must not have erythrocytosis (defined as a hematocrit of 52% or higher) attributable to other medication or medical condition
• Agree not to initiate any other treatment for erectile dysfunction (ED), including herbal and over- the-counter (OTC) medications, for the duration of the study.
• Must not already be taking finasteride or other 5-alpha reductase inhibitor

You may not qualify if…

• Men not currently using testosterone supplementation therapy or men on non-injectable testosterone therapy
• Prior history of anabolic steroid use, but have not used for at least 6 months
• Prior history of testosterone use, but have not used for at least 6 months
• Men who are already taking finasteride
• Untreated or inadequately treated hypothyroidism
• Significant history of allergy and/or sensitivity to the drug products or excipients, including sensitivity to testosterone and/or finasteride
• Current use of any medications, herbal, and/or nutritional supplements that can interfere with testosterone level
• Currently receiving treatment with cancer chemotherapy or anti-androgens
• Any contraindication to testosterone therapy or finasteride
• History of luteinizing hormone-releasing hormone antagonist or agonist treatment
• History of clomiphene treatment in 6 months prior to Visit 1

Where it is running

• Baylor College of Medicine — Houston, Texas, United States

Full record on ClinicalTrials.gov

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