Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Symptoms Associated With Menopause
Completed · Phase 3
Conditions studied: Vasomotor Symptoms Associated With Menopause
In brief
The purpose of this study is to determine whether bazedoxifene/conjugated estrogens combinations are effective in the treatment of moderate to severe vasomotor symptoms associated with menopause.
Key facts
- Study ID
- NCT00234819
- Run by
- Wyeth is now a wholly owned subsidiary of Pfizer
- People needed
- 325
- Starts
- 2005-10-01
- Expected to finish
- 2007-02-01
- Last updated by the study team
- 2007-12-28
Who can join
Age: 40 and older, up to 64. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Generally healthy, postmenopausal women, aged 40 to 64, with last natural menstrual period completed at lease 6 months ago
- Intact uterus
- Seeking treatment for hot flushes and experiencing 7 moderate to severe hot flushes per day or 50 per week
You may not qualify if…
- History of active presence of thrombophlebitis, thrombosis, thromboembolic disorders
- History of active presence of stroke, TIA, heart attack or ischemic heart disease
- History of melanoma, breast or any gynecologic cancer at any time; history of any other cancer within the past 5 years
Where it is running
- Study site — Phoenix, Arizona, United States
- Study site — Fort Myers, Florida, United States
- Study site — North Port Richey, Florida, United States
- Study site — Scarborough, Maine, United States
- Study site — Albuquerque, New Mexico, United States
- Study site — Winston-Salem, North Carolina, United States
- Study site — Pottstown, Pennsylvania, United States
Full record on ClinicalTrials.gov
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