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Completed Phase 4 Interventional

Efficacy and Safety Study in Postmenopausal Women to Determine the Lowest Effective Dose for Relief of Moderate to Severe Hot-Flushes

ClinicalTrials.gov ID: NCT00206622

Public ClinicalTrials.gov record NCT00206622. 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 18, 2026, 5:56 AM 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 Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Comparing a 2.2mg 17 Beta-Estradiol/0.69mg Levonorgestrel Combination Transdermal Patch, and a 1mg 17 Beta-Estradiol Transdermal Patch With a Placebo Patch in Postmenopausal Women to Determine the Lowest Effective Dose of Estradiol for the Relief of Moderate to Severe Hot Flushes

Brief summary

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

To determine the lowest effective dose of estradiol by comparing E2/LNG (2.2mg/0.69mg) and E2 (1.0mg) dose with placebo in decreasing the frequency and severity of moderate to severe hot flushes in postmenopausal women

Study identification

NCT ID
NCT00206622
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bayer
Industry
Enrollment
425 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2004 (Type not available)
Primary completion
Not listed
Completion
Feb 2006 (Actual)
Last update posted
May 29, 2009

2004 – 2006

United States locations

U.S. sites
45
U.S. states
24
U.S. cities
41
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801 —
Not listed Chandler Arizona 85225 —
Not listed Phoenix Arizona 85031 —
Not listed Tucson Arizona 85712 —
Not listed Fair Oaks California 95628 —
Not listed Oakland California 94612 —
Not listed San Diego California 92103 —
Not listed San Diego California 92108 —
Not listed San Diego California 92123 —
Not listed New Britain Connecticut 06050 —
Not listed West Hartford Connecticut 06117 —
Not listed Fort Myers Florida 33916 —
Not listed Gainesville Florida 32610-0254 —
Not listed Jacksonville Florida 32216 —
Not listed Tampa Florida 33613 —
Not listed West Palm Beach Florida 33409 —
Not listed Alpharetta Georgia 30005 —
Not listed Boise Idaho 83702 —
Not listed Idaho Falls Idaho 83404 —
Not listed Champaign Illinois 61820 —
Not listed Chicago Illinois 60612 —
Not listed Peoria Illinois 61615 —
Not listed South Bend Indiana 46601 —
Not listed Lexington Kentucky 40536 —
Not listed New Orleans Louisiana 70115 —
Not listed New Orleans Louisiana 70118-1034 —
Not listed Detroit Michigan 48201 —
Not listed St Louis Missouri 63110 —
Not listed Lincoln Nebraska 68510 —
Not listed Reno Nevada 89502 —
Not listed New Brunswick New Jersey 08901 —
Not listed Albuquerque New Mexico 87102 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Cincinnati Ohio 45236 —
Not listed Cleveland Ohio 44122 —
Not listed Columbus Ohio 43213 —
Not listed Philadelphia Pennsylvania 19114 —
Not listed Pittsburgh Pennsylvania 15206 —
Not listed Memphis Tennessee 38120 —
Not listed Arlington Texas 76012 —
Not listed Houston Texas 77004 —
Not listed Houston Texas 77030 —
Not listed Temple Texas 76502-1896 —
Not listed Salt Lake City Utah 84124 —
Not listed Burlington Vermont 05401-1420 —

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 NCT00206622, 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 May 29, 2009 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00206622 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →