Trials / Completed
CompletedNCT00332553
Study of Hot Flashes and Night Sweats in Postmenopausal Women Receiving Combination Raloxifene and Oral Estrogen
Study of Vasomotor Symptoms in Postmenopausal Women Receiving Combination Raloxifene and Oral Estrogen
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 150 (planned)
- Sponsor
- Eli Lilly and Company · Industry
- Sex
- Female
- Age
- 50 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
This pilot study was designed to explore the effects of combined treatment with raloxifene HCl 60 mg and oral 17 beta-estradiol 1mg/day on the number of vasomotor episodes (hot flashes plus night sweats) in postmenopausal women discontinuing continuous combined hormone replacement therapy (ccHRT) compared to women treated with raloxifene HCl 60 mg alone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Raloxifene | |
| DRUG | medroxyprogesterone acetate | |
| DRUG | estrogen | |
| DRUG | 17 beta estradiol |
Timeline
- Start date
- 2002-02-01
- Completion
- 2004-05-01
- First posted
- 2006-06-01
- Last updated
- 2007-05-15
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00332553. Inclusion in this directory is not an endorsement.