A Safety and Efficacy Study of Estradiol Vaginal Capsule in Postmenopausal Women With Vulvovaginal Atrophy
Status: | Recruiting |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 35 - Any |
Updated: | 8/10/2016 |
Start Date: | February 2016 |
End Date: | November 2016 |
Contact: | Clinical Trials Registry Team |
Email: | IR-CTRegistration@Allergan.com |
A Phase 2, Randomized, Multicenter, Double-blind, Vehicle-controlled Study to Evaluate Safety and Efficacy of Three Doses of Estradiol Vaginal Capsule in Postmenopausal Women With Vulvovaginal Atrophy
This study will access the safety and efficacy of three doses of estradiol vaginal capsules
in postmenopausal women with vulvovaginal atrophy.
in postmenopausal women with vulvovaginal atrophy.
Inclusion Criteria:
- Clinical diagnosis of vulvovaginal atrophy due to post menopause
- Age ≥ 40 years or if bilateral oophorectomy ≥ 35 years
- Moderate to severe vaginal dryness
- Normal breast exam; if > 40 years
- Vaginal pH > 5.0
- < 5% superficial cells on vaginal wall cytology smear
Exclusion Criteria:
- Known hypersensitivity to estrogen and/or progestin therapy
- Known or suspected premalignant or malignant disease
- Undiagnosed abnormal genital bleeding
- A history of or treatment for significant cardiovascular disease, congestive heart
failure, or stroke
- Active or known protein C, protein S, or antithrombin deficient, or other known
thrombophilic disorders or thromboembolic events
- Increased frequency/severity headaches with estrogen therapy
- Smokes ≥ 15 cigarettes/day
We found this trial at
20
sites
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