Vulvoscopy Changes of the Vulva, Vestibule and Vagina With Daily Ospemifene in Women With Dyspareunia From VVA

Completed · Phase 4

Conditions studied: Vulvovaginal Atrophy, Dyspareunia

In brief

This is an unblinded study to be conducted at a single research center, San Diego Sexual Medicine. Subjects meeting inclusion and exclusion criteria will receive 60 mg ospemifene daily for twenty weeks. After the informed consent is signed, a baseline physical examination, and vulvoscopy with detailed photography of the vulva, vestibule and vagina, will be performed. Physical examination and vulvoscopy with detailed photography of the vulva, vestibule and vagina, will be repeated prospectively every 4 weeks for a total of 20 weeks. Therefore, physical examination and vulvoscopy with detailed photography of the vulva, vestibule and vagina will be performed prospectively at baseline (vulvoscopy session 1), 4 weeks (vulvoscopy session 2), 8 weeks (vulvoscopy session 3), 12, weeks (vulvoscopy session 4), 16 weeks (vulvoscopy session 5) and 20 weeks (vulvoscopy session 6) following daily administration of 60 mg ospemifene.

Key facts

Study ID

NCT02784613

Run by

Sue Goldstein

People needed

10

Starts

2015-07-01

Expected to finish

2017-04-17

Last updated by the study team

2019-04-02

Who can join

Age: 21 and older, up to 80. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Subject provides written informed consent and HIPAA authorization before any study procedures are conducted
• Subject is female
• Subject is aged 21-80 years
• Subject has a body mass index (BMI) < 37 kg/m2
• Subject is menopausal either naturally (at least 12 months amenorrheic) or 6 weeks after a bilateral salpingo-oophorectomy prior to natural menopause subjects with hysterectomy only must have a serum Follicle Stimulating Hormone > 40 milli-International unit /mL
• Subject has vulvovaginal atrophy with dyspareunia
• Subject has had a normal mammogram within the last 6 months
• Subject has normal pap smear within last 6 months
• Subject has an endometrial stripe ≤ 4 mm within the last 6 months if she has a uterus
• Subject agrees to comply with the study procedures and visits.

You may not qualify if…

• Subject has a hypersensitivity to any of the ingredients of ospemifene
• Subject has used ospemifene in the past
• Subject has documented or suspected breast cancer, history of heart attack or stroke
• Subject has clinically significant findings on physical examination
• Subject has uncontrolled hypertension
• Subject has any chronic medical condition or psychologic disorder that the Principal Investigator feels makes her ineligible for the study
• Subject is currently on local or systemic androgen therapy including local or systemic testosterone (washout 14 days for local or topical androgen or non-depot injection, 1 month for depot, 6 months for pellet
• Subject is currently on local or systemic estrogen therapy or androgen therapy (washout 14 days for vaginal estrogen, 60 days for oral/transdermal therapy)
• Subject is currently using a Selective Estrogen Receptor Modulator (SERM) or products that have estrogenic or anti-estrogenic effects within last month
• Subject currently using itraconazole, ketoconazole, digitalis or alkaloids heparin or strong cytochrome P 450 3A4 inhibitors
• Subject has a history of substance abuse within 12 months prior, or consuming > 14 alcoholic drinks per week
• Subject has received an investigational drug within 30 days prior to signing consent
• Subject has any condition or exhibits behavior that indicates to the Principal Investigator that the Subject is unlikely to be compliant with study procedures and visits.

Where it is running

• San Diego Sexual Medicine — San Diego, California, United States

Full record on ClinicalTrials.gov

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