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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00108849
Other study ID # VAG-2195
Secondary ID
Status Completed
Phase Phase 3
First received April 19, 2005
Last updated February 6, 2017
Start date March 2005
Est. completion date May 2007

Study information

Verified date February 2017
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is conducted in North America. The purpose of this study is to determine if Vagifem Low Dose is an effective and safe treatment for patients suffering from postmenopausal atrophic vaginitis.


Recruitment information / eligibility

Status Completed
Enrollment 309
Est. completion date May 2007
Est. primary completion date May 2007
Accepts healthy volunteers No
Gender Female
Age group 45 Years and older
Eligibility Inclusion Criteria:

- Postmenopausal women whose last menstruation was at least two years previously

Study Design


Intervention

Drug:
estradiol, 10 mcg


Locations

Country Name City State
Canada Novo Nordisk Investigational Site Kingston
Canada Novo Nordisk Investigational Site Montreal
Canada Novo Nordisk Investigational Site Quebec City
Canada Novo Nordisk Investigational Site Toronto
Canada Novo Nordisk Investigational Site Toronto
Canada Novo Nordisk Investigational Site Winnipeg
United States Novo Nordisk Investigational Site Alpharetta Georgia
United States Novo Nordisk Investigational Site Boise Idaho
United States Novo Nordisk Investigational Site Carmichael California
United States Novo Nordisk Investigational Site Charleston South Carolina
United States Novo Nordisk Investigational Site Charlotte North Carolina
United States Novo Nordisk Investigational Site Clearwater Florida
United States Novo Nordisk Investigational Site Cleveland Ohio
United States Novo Nordisk Investigational Site Columbia South Carolina
United States Novo Nordisk Investigational Site Columbus Ohio
United States Novo Nordisk Investigational Site Daytona Beach Florida
United States Novo Nordisk Investigational Site Denver Colorado
United States Novo Nordisk Investigational Site Denver Colorado
United States Novo Nordisk Investigational Site Eugene Oregon
United States Novo Nordisk Investigational Site Evansville Indiana
United States Novo Nordisk Investigational Site Greenville South Carolina
United States Novo Nordisk Investigational Site Houston Texas
United States Novo Nordisk Investigational Site Jackson Tennessee
United States Novo Nordisk Investigational Site Lakewood Colorado
United States Novo Nordisk Investigational Site Laurel Maryland
United States Novo Nordisk Investigational Site Lawrenceville New Jersey
United States Novo Nordisk Investigational Site Lexington Kentucky
United States Novo Nordisk Investigational Site Lincoln Nebraska
United States Novo Nordisk Investigational Site Medford Oregon
United States Novo Nordisk Investigational Site Memphis Tennessee
United States Novo Nordisk Investigational Site Milwaukee Wisconsin
United States Novo Nordisk Investigational Site Mobile Alabama
United States Novo Nordisk Investigational Site Montgomery Alabama
United States Novo Nordisk Investigational Site Moorestown New Jersey
United States Novo Nordisk Investigational Site Mount Airy North Carolina
United States Novo Nordisk Investigational Site New London Connecticut
United States Novo Nordisk Investigational Site New York City New York
United States Novo Nordisk Investigational Site Norfolk Virginia
United States Novo Nordisk Investigational Site Palm Springs Florida
United States Novo Nordisk Investigational Site Palo Alto California
United States Novo Nordisk Investigational Site Peoria Illinois
United States Novo Nordisk Investigational Site Philadelphia Pennsylvania
United States Novo Nordisk Investigational Site Phoenix Arizona
United States Novo Nordisk Investigational Site Pittsburgh Pennsylvania
United States Novo Nordisk Investigational Site Plantation Florida
United States Novo Nordisk Investigational Site Roswell Georgia
United States Novo Nordisk Investigational Site San Diego California
United States Novo Nordisk Investigational Site San Diego California
United States Novo Nordisk Investigational Site Sandy Utah
United States Novo Nordisk Investigational Site Spokane Washington
United States Novo Nordisk Investigational Site Spokane Washington
United States Novo Nordisk Investigational Site Tacoma Washington
United States Novo Nordisk Investigational Site Tampa Florida
United States Novo Nordisk Investigational Site Tucson Arizona
United States Novo Nordisk Investigational Site West Palm Beach Florida
United States Novo Nordisk Investigational Site West Reading Pennsylvania
United States Novo Nordisk Investigational Site Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Countries where clinical trial is conducted

United States,  Canada, 

References & Publications (1)

Mettler L, Olsen PG. Long-term treatment of atrophic vaginitis with low-dose oestradiol vaginal tablets. Maturitas. 1991 Dec;14(1):23-31. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical symptoms after 12 months
Secondary Objective parameters (vaginal Maturation Index/Value and vaginal pH)
Secondary Hyperplasia rate
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