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Completed Phase 3 Interventional

Vagifem Low Dose for Postmenopausal Atrophic Vaginitis Symptoms

ClinicalTrials.gov ID: NCT00108849

Public ClinicalTrials.gov record NCT00108849. 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 Jul 22, 2026, 3:38 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 12 Month Double-blind, Randomized, Parallel-group, Placebo-controlled, Multi-center Trial to Investigate the Efficacy and Safety of Vagifem Low Dose (10 mcg 17beta-estradiol Vaginal Tablet) for the Treatment of Postmenopausal Atrophic Vaginitis Symptoms

Study identification

NCT ID
NCT00108849
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
309 participants

Conditions and interventions

Interventions

  • estradiol, 10 mcg Drug

Drug

Eligibility (public fields only)

Age range
45 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
Feb 28, 2005
Primary completion
Apr 30, 2007
Completion
Apr 30, 2007
Last update posted
Feb 7, 2017

2005 – 2007

United States locations

U.S. sites
51
U.S. states
26
U.S. cities
48
Facility City State ZIP Site status
Novo Nordisk Investigational Site Mobile Alabama 36608
Novo Nordisk Investigational Site Montgomery Alabama 36106
Novo Nordisk Investigational Site Phoenix Arizona 85050
Novo Nordisk Investigational Site Tucson Arizona 85712
Novo Nordisk Investigational Site Carmichael California 95608
Novo Nordisk Investigational Site Palo Alto California 94304
Novo Nordisk Investigational Site San Diego California 92108
Novo Nordisk Investigational Site San Diego California 92123
Novo Nordisk Investigational Site Denver Colorado 80218
Novo Nordisk Investigational Site Denver Colorado 80220
Novo Nordisk Investigational Site Lakewood Colorado 80228
Novo Nordisk Investigational Site New London Connecticut 06320
Novo Nordisk Investigational Site Clearwater Florida 33759
Novo Nordisk Investigational Site Daytona Beach Florida 32114
Novo Nordisk Investigational Site Palm Springs Florida 33461
Novo Nordisk Investigational Site Plantation Florida 33324
Novo Nordisk Investigational Site Tampa Florida 33607
Novo Nordisk Investigational Site West Palm Beach Florida 33409
Novo Nordisk Investigational Site Alpharetta Georgia 30005
Novo Nordisk Investigational Site Roswell Georgia 30075
Novo Nordisk Investigational Site Boise Idaho 83702
Novo Nordisk Investigational Site Peoria Illinois 61615
Novo Nordisk Investigational Site Evansville Indiana 47714
Novo Nordisk Investigational Site Lexington Kentucky 40536-0293
Novo Nordisk Investigational Site Laurel Maryland 20707
Novo Nordisk Investigational Site Lincoln Nebraska 68510
Novo Nordisk Investigational Site Lawrenceville New Jersey 08648
Novo Nordisk Investigational Site Moorestown New Jersey 08057
Novo Nordisk Investigational Site New York New York 10016
Novo Nordisk Investigational Site Charlotte North Carolina 28209
Novo Nordisk Investigational Site Mount Airy North Carolina 27030
Novo Nordisk Investigational Site Winston-Salem North Carolina 27103
Novo Nordisk Investigational Site Cleveland Ohio 44122
Novo Nordisk Investigational Site Columbus Ohio 43210
Novo Nordisk Investigational Site Eugene Oregon 97401
Novo Nordisk Investigational Site Medford Oregon 97504
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19114
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15206
Novo Nordisk Investigational Site West Reading Pennsylvania 19611
Novo Nordisk Investigational Site Charleston South Carolina 29401
Novo Nordisk Investigational Site Columbia South Carolina 29201
Novo Nordisk Investigational Site Greenville South Carolina 29607
Novo Nordisk Investigational Site Jackson Tennessee 38305
Novo Nordisk Investigational Site Memphis Tennessee 38120
Novo Nordisk Investigational Site Houston Texas 77030
Novo Nordisk Investigational Site Sandy City Utah 84070
Novo Nordisk Investigational Site Norfolk Virginia 23507
Novo Nordisk Investigational Site Spokane Washington 99204
Novo Nordisk Investigational Site Spokane Washington 99207
Novo Nordisk Investigational Site Tacoma Washington 98405
Novo Nordisk Investigational Site Milwaukee Wisconsin 53209

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00108849, 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 Feb 7, 2017 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00108849 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →