Evaluate the Safety and Efficacy of Bremelanotide in Women With Female Sexual Arousal Disorder (FSAD)
- Conditions
- Sexual Arousal Disorder
- Registration Number
- NCT00425256
- Lead Sponsor
- Palatin Technologies, Inc
- Brief Summary
This 8 week at home study is designed to explore efficacy endpoints and evaluate the safety of intranasal Bremelanotide in women with Female Sexual Arousal Disorder. Efficacy will be assessed vs. a parallel placebo group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- Not specified
- Post menopausal and in general good health
- In a stable relationship with a male partner for at least 6 months
- Willing to attempt sexual activity once a week with your partner
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (20)
Medical Affiliated Research Center
🇺🇸Huntsville, Alabama, United States
Quality of Life Medical & Research Center, LLC
🇺🇸Tucson, Arizona, United States
University of California, Department of Family and Preventative Medicine
🇺🇸LaJolla, California, United States
Downtown Women's Health Care
🇺🇸Denver, Colorado, United States
Coastal Connecticut Research
🇺🇸New London, Connecticut, United States
South Florida Medical Research
🇺🇸Aventura, Florida, United States
Clinical Study Center
🇺🇸Ft. Myers, Florida, United States
Center For Marital and Sexual Health of South Florida
🇺🇸West Palm Beach, Florida, United States
Northeast Indiana Research
🇺🇸Fort Wayne, Indiana, United States
Center for Sexual Medicine at Sheppard Pratt
🇺🇸Baltimore, Maryland, United States
Scroll for more (10 remaining)Medical Affiliated Research Center🇺🇸Huntsville, Alabama, United States