Study to Evaluate the Effects of Synthetic Conjugated Estrogens, B (SCE-B) on Nocturnal Vasomotor Symptoms in Postmenopausal Women
Public ClinicalTrials.gov record NCT00592839. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 4, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of SCE-B on Nocturnal Vasomotor Symptoms in Postmenopausal Women
Study identification
- NCT ID
- NCT00592839
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 4
- Lead sponsor
- Duramed Research
- Industry
- Enrollment
- 157 participants
Conditions and interventions
Conditions
Interventions
- SCE-B Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 30 Years to 65 Years
- Sex
- Female
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Nov 30, 2007
- Primary completion
- Jan 31, 2009
- Completion
- Jan 31, 2009
- Last update posted
- Jul 18, 2013
2007 – 2009
United States locations
- U.S. sites
- 17
- U.S. states
- 12
- U.S. cities
- 17
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Duramed Investigational Site | Anaheim | California | 92801 | — |
| Duramed Investigational Site | Sacramento | California | 95821 | — |
| Duramed Investigational Site | San Diego | California | 92108 | — |
| Duramed Investigational Site | Clearwater | Florida | 33759 | — |
| Duramed Investigational Site | West Palm Beach | Florida | 33409 | — |
| Duramed Investigational Site | Lexington | Kentucky | 40509 | — |
| Duramed Investigational Site | Louisville | Kentucky | 40291 | — |
| Duramed Investigational Site | Lincoln | Nebraska | 68510 | — |
| Duramed Investigational Site | Moorestown | New Jersey | 08057 | — |
| Duramed Investigational Site | Albuquerque | New Mexico | 87102 | — |
| Duramed Investigational Site | Winston-Salem | North Carolina | 27103 | — |
| Duramed Investigational Site | Cleveland | Ohio | 44122 | — |
| Duramed Investigational Site | Mayfield Heights | Ohio | 44124 | — |
| Duramed Investigational Site | Medford | Oregon | 97504 | — |
| Duramed Investigational Site | Pittsburgh | Pennsylvania | 15206 | — |
| Duramed Investigational Site | Columbia | South Carolina | 29201 | — |
| Duramed Investigational Site | San Antonio | Texas | 78229 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00592839, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jul 18, 2013 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00592839 live on ClinicalTrials.gov.