Female Sexual Arousal Disorder Clinical Trials
We have a research study available for pre-menopausal women with Female Sexual Arousal Disorder (FSAD). The purpose of this research study is to find safer and more effective medications for individuals with FSAD.
The investigational medication will be provided at no cost and compensation is provided for time and travel. No health insurance is required to participate in any of our depression studies.
Participate in a Female Sexual Arousal Disorder (FSAD) Research Study
Fill out the contact form below and one of our Recruitment Specialists will contact you within 48 hours with more study information.
You can also call us now at (714) 289-1100.
What is Female Sexual Arousal Disorder (FSAD)?
Female Sexual Arousal Disorder (FSAD) is a persistent or recurrent inability to attain, or to maintain until completion of the sexual activity, an adequate lubrication-swelling response of sexual excitement that causes marked distress or interpersonal difficulty. Orgasm is not possible without arousal and lack of arousal commonly leads to a lack of desire because sexual activity is not enjoyable.
This disorder is estimated to negatively impact ~20% of US women and affects ~40% of US women at some point during their lives. Despite the high prevalence of FSAD and the potential impact impaired arousal has on other aspects of sexual function in women, to date there are no FDA-approved pharmacological treatments for FSAD.
The purpose of this clinical research study is to determine the safety and effectiveness of an investigational medication in improving symptoms of FSAD in pre-menopausal patients.
Unsure if you have Female Sexual Arousal Disorder (FSAD)?
Call us at (714) 298-1100 for a free phone consultation.
Female Sexual ArousaL Disorder Clinical Trials
If you answer YES to all of the following questions then you may qualify for our depression clinical trials.
1. Are you a female that is 21 years or older?
2. Are you currently experiencing trouble attaining or maintaining sexual arousal?
3. Are you pre-menopausal?
4. Are you in a stable monogamous relationship, for at least 6 months?
5. Are you willing to take study medication?
Final eligibility is determined during a screening visit at our study site at Orange. During this visit, you will:
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Meet with a professional physician, psychiatrist, and/or psychologist and be interviewed about your mental and physical health
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Review additional information
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Undergo a physical examination and have your vitals taken
If you qualify and decide to participate:
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A study doctor will closely monitor you, your symptoms, and overall health
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All study-related medical care and study medication will be provided at no cost
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Transportation may be provided at no cost if you need assistance
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You will sign an Informed Consent Form (ICF) which outlines which procedures you can expect during each visit
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You will be compensated for each completed visit
*A list of common procedures involved when participating in a clinical trial can be found here.
Contact Us
We can be reached Monday through Friday, 8am - 5:30pm
Abigail C. Parera
Call (714) 289-1100
Text (714) 559-3198
NRC Research Institute
1010 W. Chapman Ave.
Orange, CA 92868
