Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD) - Second Study



Status:Not yet recruiting
Conditions:Neurology, Psychiatric
Therapuetic Areas:Neurology, Psychiatry / Psychology
Healthy:No
Age Range:40 - 80
Updated:3/10/2019
Start Date:October 2019
End Date:March 2021
Contact:Marie-Christine Dumas
Email:marie-christine.dumas@endoceutics.com
Phone:1-855-653-0033

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Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD) - Second Study (Placebo-Controlled, Double-Blind and Randomized Phase III Study of Intravaginal Prasterone)

The primary objective is to confirm the efficacy of intravaginal prasterone (DHEA) on
Hypoactive Sexual Desire Disorder (HSDD) in postmenopausal women.


Inclusion Criteria (main criteria):

- Postmenopausal women (hysterectomized or not).

- Women between 40 and 80 years of age.

- Being in a stable relationship with the opportunity for sexual activity or
masturbation at least once a month during the last 6 months or longer (before
screening visit) and during the following 8 months.

- Diagnosis of HSDD confirmed by a qualified clinician.

- Willing to participate in the study and sign an informed consent.

Exclusion Criteria (main criteria):

- Chronic or acute life stress or major life change that could have interfered and
continues to interfere significantly with sexual activity.

- Taking drugs which could be responsible for HSDD.

- Severe medical condition which can explain the loss of sexual desire.

- The administration of any investigational drug within 30 days of screening visit.

- Clinically significant abnormal serum biochemistry, urinalysis or hematology.
We found this trial at
10
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Huntsville, Alabama 35801
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Bluffton, South Carolina 29910
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Fargo, North Dakota 58103
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New London, Connecticut 06320
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New York, New York 10016
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Roswell, Georgia 30075
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Saint Petersburg, Florida 33709
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Saint Petersburg, FL
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San Antonio, Texas 78205
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San Antonio, TX
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San Diego, California 92120
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San Diego, CA
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Savannah, Georgia 31406
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Savannah, GA
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