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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 Sep 3, 2026, 2:31 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
Nov 30, 2004
Primary completion
Not listed
Completion
Jan 31, 2006
Last update posted
May 28, 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 28, 2009 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00206622 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →