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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Study to Evaluate the Effects of Synthetic Conjugated Estrogens, B (SCE-B) on Nocturnal Vasomotor Symptoms in Postmenopausal Women

ClinicalTrials.gov ID: NCT00592839

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.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 10:20 PM EDT

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multi-center study to evaluate the effects of SCE-B on nocturnal vasomotor symptoms. Study duration will be approximately 16 weeks; this includes a 4-week screening period and approximately 5 scheduled clinic visits. Participants will receive one of two strengths of SCE-B tablets plus matching placebo or placebo only, and will have a physical and gynecological exams that may include transvaginal ultrasound, endometrial biopsy and a pap smear. Participants will be asked to wear a monitoring device for a portion of the study and be asked to complete a daily dairy.

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

Interventions

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
Dec 2007 (Type not available)
Primary completion
Feb 2009 (Actual)
Completion
Feb 2009 (Actual)
Last update posted
Jul 19, 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 19, 2013 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00592839 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →