Has your libido or sexual arousal previoulsy been at a “normal” level for at least 2 years in the past, but currently one or the other is decreased?
Premenopausal females are invited to participate in this research study being conducted at the PRO-Salt Lake Women’s Center clinic; Michael L. Twede, MD, FACOG and Colorado PRO-Red Rocks OB/GYN Clinic; Gail B. Womack, MD, FACOG.
This is an approximate 23-week study requiring 12-13 clinic visits. Study medication is being evaluated with placebo (1 in 4 chance of receiving placebo). Qualified participants will be required to perform self injections (like a flu shot) with the study medication. Injection training is provided during study.
You may qualify if you meet the above description and you:
Are a premenopausal female aged 21 and up.
Are currently in a sexual relationship (male or female) that has been stable for at least six months.
Can agree to engage in sexual activity at least once per month during study particpation (in your own “home” privacy).
Can agree to use a medically acceptable form of birth control/are not nursing or planning to become pregnant during study.
Do not have a unresolved sexual trauma or abuse history.
Can attend three (3), “six-hour long” clinic visits.
Can agree to wear a “take home” ambulatory blood pressure monitor for three, 24-hour periods during study.
Other qualifications apply.
Qualified participants receive no cost: study medical evaluations, study laboratory tests, study counseling, study medication or placebo. Time and travel compensation up to $900.00 to qualified participants.
Complete the Inquiry Form to the right and Submit, OR, Contact Research Staff at the Clinics:
PRO – Salt Lake Women’s Center/Sandy, UT: 801-352-9228
PRO – Red Rocks Ob/GYN, Lakewood, CO: 303-985-9100
