CURRENT CENTER FOR SEXUAL MEDICINE CLINICAL TRIALS
Study Information Study Description
Enrollment Dates:
2/1/2007 12:00:00 AM - 2/2/2011 12:00:00 AM

Diagnosis:
Hypoactive Sexual Desire Disorder - 8.5 months Libigel

Population:
  • Adult Female

    Setting:
    Outpatient

    Duration:
    8.5 months Libigel
    		• Bloom 006 Study: This randomized, placebo-controlled 6 month study will evaluate an investigational medication, LibiGel (testosterone gel), for the treatment of Hypoactive Sexual Desire Disorder. Hypoactive Sexual Desire Disorder includes a loss of sexual desire that causes distress for the woman and her relationship. Generally healthy women 30-65 yrs old who are menopausal due to hysterectomy and bilateral oophorectomy, and who are experiencing a distressing loss of sexual desire may participate. All participants must be taking an appropriate form of estrogen therapy throughout the duration of the study. Patients will be compensated for their time.
    Enrollment Dates:
    4/14/2008 12:00:00 AM - 11/1/2011 12:00:00 AM

    Diagnosis:
    Hypoactive Sexual Desire Disorder - 3 to 5 years Libigel

    Population:
  • Adult Female

    Setting:
    Outpatient

    Duration:
    3 to 5 years Libigel
    		• Bloom 007 Study: This randomized, placebo-controlled 5 year study will evaluate an investigational medication, LibiGel (testosterone gel), for the treatment of Hypoactive Sexual Desire Disorder. Hypoactive Sexual Desire Disorder includes a loss of sexual desire that causes distress for the woman and her relationship. Generally healthy women at least 50 yrs of age who are menopausal, and who are experiencing a distressing loss of sexual desire may participate. This study will be evaluating safety in women with existing cardiovascular risk factors such as high blood pressure or smoking. Both women who are on estrogen, and women who are not on estrogen, may participate. Patients will be compensated for their time.
    Enrollment Dates:
    5/1/2008 12:00:00 AM - 10/1/2014 12:00:00 AM

    Diagnosis:
    Hypoactive Sexual Desire Disorder - 3 year Registry

    Population:
  • Adult Female

    Setting:
    Outpatient

    Duration:
    3 year Registry
    		• HSDD Registry Study: This is a non-treatment study which will follow the natural progression of Hypoactive Sexual Desire Disorder in women. Hypoactive Sexual Desire Disorder includes a loss of sexual desire that causes distress for the woman and her relationship. Study activities include informed consent, an initial interview, and completing questionnaires every 3 months on your home computer or by mail. The questionnaires take about 30 minutes to complete. No medications or treatments are involved. Patients will be compensated for their time.
    Enrollment Dates:
    10/13/2009 12:00:00 AM - 10/22/2010 12:00:00 AM

    Diagnosis:
    Hypoactive Sexual Desire Disorder - 9 month Bouquet

    Population:
  • Adult Female

    Setting:
    Outpatient

    Duration:
    9 month Bouquet
    		• Bouquet Study for Menopausal Women: This randomized, placebo-controlled 8 month study will evaluate an investigational medication for the treatment of Hypoactive Sexual Desire Disorder. Hypoactive Sexual Desire Disorder includes a loss of sexual desire that causes distress for the woman and her relationship. Generally healthy women who have experienced menopause (no longer menstruating for >1yr), and who are experiencing a distressing loss of sexual desire may participate. Patients will be compensated for their time. Please call the Center study line for more information 410-938-4344.


     If you are interested in participating in one of the above studies, please complete the form below to submit your contact information. You may also contact the Center for Sexual Medicine at 410-938-4342.

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    Last modified: Wednesday, September 08, 2010

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