Effect of Testosterone Therapy in Men With Alzheimer's Disease and Low Testosterone

Completed · Not applicable

Conditions studied: Alzheimer's Disease, Hypogonadism

In brief

Treatment with testosterone can improve performance on tests of spatial ability in men with low testosterone levels and Alzheimer's disease. Improved performance on these tests may mean an improved ability to get around in one's environment without getting lost or injured. This could have a positive impact on both patients and those who care for them. We will investigate what areas of the brain are involved in these improvements in spatial ability. This will be done using a PET scan, which creates a 3-dimensional image of the brain that can allow us to see how the brain functions.

Key facts

Study ID

NCT00392912

Run by

Michael E. DeBakey VA Medical Center

People needed

10

Starts

2007-04-01

Expected to finish

2010-07-01

Last updated by the study team

2010-08-19

Who can join

Age: 55 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Alzheimer's disease diagnosis, based on Diagnostic and Statistical Manual of Mental Disorders (5th ed.; DSM-V)
• Total testosterone < 300 ng/dL and/or calculated free testosterone < 50 pg/ml
• Sufficient English to perform cognitive testing
• Stable on concomitant medications for 1 month prior to starting study

You may not qualify if…

• history of prostate cancer
• history of breast cancer
• gonadal endocrine disorders
• current major psychiatric illness (excluding depression)
• significant uncontrolled systemic illness
• recent myocardial infarction (within 6 months)
• renal or hepatic disease, sleep apnea
• history of alcoholism or substance abuse within the past year
• history of head injury with loss of consciousness greater than 1 hour
• testosterone or other androgen treatment within past 3 months
• history of taking other drugs that might interfere with the results of the study (ie, spironolactone, cimetidine, antiandrogens, estrogens, p450 enzyme inducers, barbiturates)
• symptomatic BPH: prostatic symptoms, prostatic masses or induration on rectal examination
• prostate specific antigen (PSA) >4.0 mg/mL
• hemoglobin > 17 mg/dL
• generalized skin disease that could affect the absorption of testosterone gel (ie, psoriasis).
• potentially agitated or uncooperative for procedures

Where it is running

• Michael E. DeBakey VA Medical Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.