Low-dose Hormone Therapy for Relief of Vasomotor Symptoms

Completed · Phase 3 · Has a placebo group

Conditions studied: Vasomotor Symptoms, Hot Flashes

In brief

The purpose of this study is to determine the lowest effective dose of the study drug for the relief of moderate to severe vasomotor symptoms in postmenopausal women for 12 weeks.

Key facts

Study ID

NCT00446199

Run by

Bayer

People needed

735

Starts

2007-03-01

Expected to finish

2008-11-01

Last updated by the study team

2015-05-06

Who can join

Age: 40 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Postmenopausal women >40 years of age experiencing a minimum of 7 to 8 moderate to severe hot flushes per day or 50 to 60 moderate to severe hot flushes per week

You may not qualify if…

• The usual exclusion criteria for hormone therapy apply
• Intake of medications other than hormones affecting hot flushes

Where it is running

• Study site — Chandler, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Paramount, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — Valley Village, California, United States
• Study site — Vista, California, United States
• Study site — Colorado Springs, Colorado, United States
• Study site — Denver, Colorado, United States
• Study site — New Britain, Connecticut, United States
• Study site — Boynton Beach, Florida, United States
• Study site — Clearwater, Florida, United States
• Study site — Daytona Beach, Florida, United States
• Study site — Fort Myers, Florida, United States
• Study site — Jacksonville, Florida, United States
• Study site — Lake Worth, Florida, United States
• Study site — Leesburg, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Mobile, Alabama, United States

Full record on ClinicalTrials.gov

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