Study Evaluating the Efficacy of DVS-233 in Fibromyalgia

NCT ID: NCT00301431

Last Updated: 2007-12-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

1050 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-08-31

Study Completion Date

2007-06-30

Brief Summary

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The purpose of this study is to determine if DVS-233 is safe and effective in the treatment of pain and other symptoms of fibromyalgia syndrome.

Detailed Description

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Conditions

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Fibromyalgia

Keywords

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Fibromyalgia Adults Outpatients Adult Double-Blind Method

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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DVS-233

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Fibromyalgia according to 1990 American College of Rheumatology (ACR) criteria

Exclusion Criteria

* Other painful conditions that may make results difficult to interpret.
* Treatment with other drugs for fibromyalgia with 14 days of study start or during the study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Wyeth is now a wholly owned subsidiary of Pfizer

INDUSTRY

Sponsor Role lead

Principal Investigators

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Medical Monitor

Role: STUDY_DIRECTOR

Wyeth is now a wholly owned subsidiary of Pfizer

Locations

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Huntsville, Alabama, United States

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Mobile, Alabama, United States

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Phoenix, Arizona, United States

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Anaheim, California, United States

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Sacramento, California, United States

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San Diego, California, United States

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Santa Ana, California, United States

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Walnut Creek, California, United States

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Denver, Colorado, United States

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Cromwell, Connecticut, United States

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Brooksville, Florida, United States

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DeLand, Florida, United States

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Delray Beach, Florida, United States

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Jacksonville, Florida, United States

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Miami, Florida, United States

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Palm Beach Gardens, Florida, United States

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Pembroke Pines, Florida, United States

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St. Petersburg, Florida, United States

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Sunrise, Florida, United States

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Tamarac, Florida, United States

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Tampa, Florida, United States

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Atlanta, Georgia, United States

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Decatur, Georgia, United States

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Smyrna, Georgia, United States

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Chicago, Illinois, United States

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Chicago, Illinois, United States

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Indianapolis, Indiana, United States

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Lexington, Kentucky, United States

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Lexington, Kentucky, United States

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Rockville, Maryland, United States

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Boston, Massachusetts, United States

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Newton, Massachusetts, United States

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Lansing, Michigan, United States

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Kansas City, Missouri, United States

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St Louis, Missouri, United States

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Las Vegas, Nevada, United States

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Clementon, New Jersey, United States

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Raleigh, North Carolina, United States

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Cincinnati, Ohio, United States

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Dayton, Ohio, United States

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Oklahoma City, Oklahoma, United States

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Oklahoma City, Oklahoma, United States

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Tulsa, Oklahoma, United States

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Duncansville, Pennsylvania, United States

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Harleysville, Pennsylvania, United States

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Philadelphia, Pennsylvania, United States

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Philadelphia, Pennsylvania, United States

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Sellersville, Pennsylvania, United States

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West Reading, Pennsylvania, United States

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Warwick, Rhode Island, United States

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Charleston, South Carolina, United States

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Summerville, South Carolina, United States

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Bristol, Tennessee, United States

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Chattanooga, Tennessee, United States

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Memphis, Tennessee, United States

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Austin, Texas, United States

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Dallas, Texas, United States

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San Antonio, Texas, United States

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Middleton, Wisconsin, United States

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Countries

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United States

Other Identifiers

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3151A4-327

Identifier Type: -

Identifier Source: org_study_id