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Hypoactive Sexual Desire Disorder (HSDD) in Postmenopausal Women

  • November 16, 2017

The purpose of this study is to confirm the effectiveness of daily intravaginal administration of an prasterone for 28 weeks on Hypoactive Sexual Desire Disorder in postmenopausal women, as compared to a placebo.

Duration:  Approximately 8 months

Number of visits to CKRA:  Up to 6

Compensation:  Up to $425 for time and travel

Note:  Qualified participants must be postmenopausal women between the ages of 40 and 80 years of age whose HSDD is not the result of any acute or chronic life stress, major life change, sexual trauma or abuse, or medical disease or disorder.  Other criteria also apply.

Hypoactive Sexual Desire Disorder in Postmenopausal Women Study

If you are interested in participating in this study, please fill out the form below. This will help us determine if you meet some of the initial criteria necessary to participate. We will contact you within 48 hours to follow up and clarify any questions that you, or we, may have. If it is determined that you meet all of the initial criteria, you may be scheduled to come in for your first visit, which is considered a screening visit. At this visit, Dr. Adams and the study coordinator will determine if you meet all of the criteria required to participate. Per CKRA's privacy policy, all of your personal information that we have obtained will be kept in our secure database, which can only be accessed by authorized CKRA personnel, unless given your permission or except as required by law.
  • Prequalifying Questionnaire

    No periods for at least the past year for non-hysterectomized women, or hysterectomized women who were premenopausal at the time of they hysterectomy, or bilateral oophorectomy with or without hysterectomy at least 6 months ago.