Study to Evaluate Divigel for the Treatment of Postmenoupausal Symptoms
NCT00727129 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 495
Last updated 2008-09-26
Summary
The purpose of this study is to compare the safety and efficacy of USL-221 to placebo for postmenopausal patients.
Conditions
- Postmenopausal Symptoms
Interventions
- DRUG
-
Divigel
Sponsors & Collaborators
-
Upsher-Smith Laboratories
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-07-31
- Completion
- 2005-08-31
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