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Completed Phase 3 Interventional

Study Evaluating Conjugated Estrogen Cream for Atrophic Vaginitis

ClinicalTrials.gov ID: NCT00137371

Public ClinicalTrials.gov record NCT00137371. 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 20, 2026, 5:36 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

Efficacy and Safety of 2 Low-Dose Regimens of Conjugated Estrogen Cream Administered Vaginally in Postmenopausal Women With Atrophic Vaginitis

Brief summary

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

This protocol is designed to study the effect and safety of 2 low-dose regimens of conjugated estrogen cream (PVC) given vaginally in postmenopausal women with atrophic vaginitis.

Study identification

NCT ID
NCT00137371
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
480 participants

Conditions and interventions

Eligibility (public fields only)

Age range
45 Years to 80 Years
Sex
Female
Healthy volunteers
Not listed

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

Study timeline

Start date
Aug 2005 (Type not available)
Primary completion
Not listed
Completion
Sep 2007 (Actual)
Last update posted
Dec 10, 2007

2005 – 2007

United States locations

U.S. sites
32
U.S. states
16
U.S. cities
31
Facility City State ZIP Site status
Not listed Tucson Arizona 85715 —
Not listed Encinitas California 92024 —
Not listed San Diego California 92108 —
Not listed Torrance California 90502 —
Not listed Aurora Colorado 80010 —
Not listed Brooksville Florida 34613 —
Not listed Miami Florida 33186 —
Not listed St. Petersburg Florida 33709 —
Not listed Tampa Florida 33066 —
Not listed West Palm Beach Florida 33407 —
Not listed Atlanta Georgia 30328 —
Not listed Augusta Georgia 30901 —
Not listed Chicago Illinois 60612 —
Not listed Metairie Louisiana 70006 —
Not listed Troy Michigan 48084 —
Not listed St Louis Missouri 63141 —
Not listed Omaha Nebraska 68134 —
Not listed New Brunswick New Jersey 08901 —
Not listed Chapel Hill North Carolina 27514 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Oklahoma City Oklahoma 73112 —
Not listed Danville Pennsylvania 17822-2920 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Pittsburgh Pennsylvania 15206 —
Not listed Carrollton Texas 75006 —
Not listed Carrollton Texas 75010 —
Not listed Colleyville Texas 76034 —
Not listed Dallas Texas 75246 —
Not listed Houston Texas 77030 —
Not listed Plano Texas 75093 —
Not listed Charlottesville Virginia 22903 —
Not listed Norfolk Virginia 23502 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00137371, 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 Dec 10, 2007 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00137371 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →