Vagifem Low Dose for Postmenopausal Atrophic Vaginitis Symptoms

This study has been completed.

Sponsor:

Information provided by:

Novo Nordisk

ClinicalTrials.gov Identifier:

NCT00108849

First received: April 19, 2005

Last updated: March 19, 2012

Last verified: March 2012

History of Changes

Purpose

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.

Condition	Intervention	Phase
Menopause Postmenopausal Vaginal Atrophy	Drug: estradiol, 10 mcg	Phase 3

Study Type:	Interventional
Study Design:	Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment
Official Title:	Efficacy and Safety of Vagifem Low Dose for Postmenopausal Atrophic Vaginitis Symptoms

Resource links provided by NLM:

MedlinePlus related topics: Menopause

Drug Information available for: Estradiol Estradiol cypionate Estradiol valerate Estradiol acetate Estradiol hemihydrate

U.S. FDA Resources

Further study details as provided by Novo Nordisk:

Primary Outcome Measures:

Clinical symptoms [ Time Frame: after 12 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

Objective parameters (vaginal Maturation Index/Value and vaginal pH) [ Designated as safety issue: No ]
Hyperplasia rate [ Designated as safety issue: Yes ]

Enrollment:	309
Study Start Date:	March 2005
Study Completion Date:	May 2007
Primary Completion Date:	May 2007 (Final data collection date for primary outcome measure)

Eligibility

Ages Eligible for Study:	45 Years and older
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Postmenopausal women whose last menstruation was at least two years previously

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00108849

Locations

United States, Nevada
Novo Nordisk Clinical Trial Call Center
Las Vegas, Nevada, United States, 89103

Sponsors and Collaborators

Novo Nordisk

Investigators

Study Director:

Alan Moses, MD

Novo Nordisk

More Information

Additional Information:

Clinical Trials at Novo Nordisk This link exits the ClinicalTrials.gov site

No publications provided by Novo Nordisk

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Simon J, Nachtigall L, Ulrich LG, Eugster-Hausmann M, Gut R. Endometrial safety of ultra-low-dose estradiol vaginal tablets. Obstet Gynecol. 2010 Oct;116(4):876-83.

Simon J, Nachtigall L, Gut R, Lang E, Archer DF, Utian W. Effective treatment of vaginal atrophy with an ultra-low-dose estradiol vaginal tablet. Obstet Gynecol. 2008 Nov;112(5):1053-60.

Responsible Party:	Public Access to Clinical Trials, Novo Nordisk A/S
ClinicalTrials.gov Identifier:	NCT00108849 History of Changes
Other Study ID Numbers:	VAG-2195
Study First Received:	April 19, 2005
Last Updated:	March 19, 2012
Health Authority:	Canada: Health Canada United States: Food and Drug Administration

Additional relevant MeSH terms:

Vaginitis
Atrophy
Vaginal Diseases
Genital Diseases, Female
Pathological Conditions, Anatomical
Estradiol

Estrogens
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on May 19, 2013

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