Testosterone Replacement in Male Cancer Survivors With Fatigue and Low Testosterone (NCT04049331)
Improving Patient-Important Outcomes With Testosterone Replacement in Hypogonadal Men With a Prior History of Cancer
๐ฉบ Plain-English Summary (8th-Grade Level)
The overall goal of this study is to evaluate the effect of a testosterone drug called Depo-Testosterone (or 'testosterone cypionate'), an FDA-approved drug for improving fatigue, sexual function, quality of life, body composition, muscle strength, and physical activity in young cancer survivors who report fatigue and have low testosterone. Main hypothesis is that Testosterone administration in young male cancer survivors who are in remission for at least 1 year, report cancer-related fatigue and have symptomatic testosterone deficiency will be associated with greater improvements in fatigue scores compared with placebo.
Who can join: Review the eligibility criteria below.
Location: Brigham and Women's Hospital โ Boston, Massachusetts
Age range: 18 Years to 54 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (2 Sites)
- Brigham and Women's Hospital โ Boston, Massachusetts
- Veterans Affairs Puget Sound Health Care System โ Seattle, Washington
๐ Contact the Study Coordinator
Phone: (206) 764-2984
Email: jg77@uw.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hypogonadism, Male
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- Improving Cancer-related Fatigue, Sexual Dysfunction and Quality of Life in Older Men With Cancer and Androgen Deficiency โ Augusta, Georgia
- Ambulatory Blood Pressure Monitoring (ABPM) Study in Hypogonadal Men โ Birmingham, Alabama
- 52 Week Study + 24-Month Long-Term Extension of Safety, PK, & Efficacy of XYOSTEDยฎ for Testosterone Replacement in Male Adolescents With Hypogonadism โ Los Angeles, California
- Testosterone Treatment in Men With Chronic Kidney Disease โ St Louis, Missouri
Explore by condition: All Hypogonadism, Male clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.