Male volunteers needed for a Low Testosterone research study

  • STATUS
    Recruiting
Updated on 23 November 2020

Summary

Male volunteers needed for a Low Testosterone research study

Description

The study is evaluating the effectiveness of an investigational gel that is delivered with a pump/cap applicator for the treatment of low testosterone symptoms (such as low sex drive, low energy, mood problems, loss of muscle mass). Men who currently treat or do not treat their low testosterone are welcome to volunteer.

If you are eligible and decide to volunteer, you can expect 12 office visits over approximately 5 months.

Monetary compensation is available for those who volunteer and qualify. No health insurance is required. If you have never been diagnosed with low testosterone but suffer from the symptoms please call for a free low testosterone screen.

If you are interested in learning more about this study, please contact Coastal Carolina Research Center at 856-3784 (856-DRUG). You may also text STUDY to 72727 or apply online at www.coastalcarolinaresearch.com . Referrals to your family members, friends or co-workers would be appreciated as we cannot do our work without the support of the Low Country community.

All research study-related care is provided to qualified participants at no cost including:

  • Investigational medication or placebo
  • Physical exam
  • Lab work

Details
Clinical Study IdentifierTX138853
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

To qualify you must
Be male between 18 and 75 years of age
Testosterone levels below 300 mg/dL
Be in good general health
Clear my responses

How to participate?

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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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