- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00282997
A Safety Study Of Pregabalin In Fibromyalgia
January 21, 2021 updated by: Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
A 12-Week, Open-Label, Safety Trial Of Pregabalin In Patients With Fibromyalgia
To evaluate the safety of pregabalin in patients with fibromyalgia.
Study Overview
Study Type
Interventional
Enrollment
500
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Arkansas
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Little Rock, Arkansas, United States
- Pfizer Investigational Site
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California
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Fresno, California, United States
- Pfizer Investigational Site
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La Jolla, California, United States
- Pfizer Investigational Site
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Northridge, California, United States
- Pfizer Investigational Site
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Pismo Beach, California, United States
- Pfizer Investigational Site
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Sacramento, California, United States
- Pfizer Investigational Site
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San Diego, California, United States
- Pfizer Investigational Site
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Walnut Creek, California, United States
- Pfizer Investigational Site
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Delaware
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Newark, Delaware, United States
- Pfizer Investigational Site
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Florida
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DeLand, Florida, United States
- Pfizer Investigational Site
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Gainesville, Florida, United States
- Pfizer Investigational Site
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Hollywood, Florida, United States
- Pfizer Investigational Site
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Melbourne, Florida, United States
- Pfizer Investigational Site
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Ocala, Florida, United States
- Pfizer Investigational Site
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Palm Harbor, Florida, United States
- Pfizer Investigational Site
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Sunrise, Florida, United States
- Pfizer Investigational Site
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Tampa, Florida, United States
- Pfizer Investigational Site
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West Palm Beach, Florida, United States
- Pfizer Investigational Site
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Illinois
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Gurnee, Illinois, United States
- Pfizer Investigational Site
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Moline, Illinois, United States
- Pfizer Investigational Site
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Indiana
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Indianapolis, Indiana, United States
- Pfizer Investigational Site
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Iowa
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Dubuque, Iowa, United States
- Pfizer Investigational Site
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Kansas
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Prairie Village, Kansas, United States
- Pfizer Investigational Site
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Pratt, Kansas, United States
- Pfizer Investigational Site
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Kentucky
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Lexington, Kentucky, United States
- Pfizer Investigational Site
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Louisiana
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Kenner, Louisiana, United States
- Pfizer Investigational Site
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Metairie, Louisiana, United States
- Pfizer Investigational Site
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Massachusetts
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North Dartmouth, Massachusetts, United States
- Pfizer Investigational Site
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Watertown, Massachusetts, United States
- Pfizer Investigational Site
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Worcester, Massachusetts, United States
- Pfizer Investigational Site
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Minnesota
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Chaska, Minnesota, United States
- Pfizer Investigational Site
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Saint Paul, Minnesota, United States
- Pfizer Investigational Site
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Missouri
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Jefferson City, Missouri, United States
- Pfizer Investigational Site
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Kansas City, Missouri, United States
- Pfizer Investigational Site
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Saint Louis, Missouri, United States
- Pfizer Investigational Site
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Nebraska
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Lincoln, Nebraska, United States
- Pfizer Investigational Site
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New Jersey
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Morristown, New Jersey, United States
- Pfizer Investigational Site
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New York
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Albany, New York, United States
- Pfizer Investigational Site
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Endwell, New York, United States
- Pfizer Investigational Site
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New York, New York, United States
- Pfizer Investigational Site
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West Seneca, New York, United States
- Pfizer Investigational Site
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North Carolina
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Asheville, North Carolina, United States
- Pfizer Investigational Site
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Hickory, North Carolina, United States
- Pfizer Investigational Site
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Raleigh, North Carolina, United States
- Pfizer Investigational Site
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Salisbury, North Carolina, United States
- Pfizer Investigational Site
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Winston-Salem, North Carolina, United States
- Pfizer Investigational Site
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North Dakota
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Minot, North Dakota, United States
- Pfizer Investigational Site
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Ohio
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Cincinnati, Ohio, United States
- Pfizer Investigational Site
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Dayton, Ohio, United States
- Pfizer Investigational Site
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Oklahoma
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Tulsa, Oklahoma, United States
- Pfizer Investigational Site
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Pennsylvania
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Bethlehem, Pennsylvania, United States
- Pfizer Investigational Site
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Norristown, Pennsylvania, United States
- Pfizer Investigational Site
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South Carolina
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Goose Creek, South Carolina, United States
- Pfizer Investigational Site
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Mount Pleasant, South Carolina, United States
- Pfizer Investigational Site
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Myrtle Beach, South Carolina, United States
- Pfizer Investigational Site
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Summerville, South Carolina, United States
- Pfizer Investigational Site
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Tennessee
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Knoxville, Tennessee, United States
- Pfizer Investigational Site
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Milan, Tennessee, United States
- Pfizer Investigational Site
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Nashville, Tennessee, United States
- Pfizer Investigational Site
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Texas
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Bedford, Texas, United States
- Pfizer Investigational Site
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Georgetown, Texas, United States
- Pfizer Investigational Site
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Houston, Texas, United States
- Pfizer Investigational Site
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Killeen, Texas, United States
- Pfizer Investigational Site
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Lake Jackson, Texas, United States
- Pfizer Investigational Site
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San Antonio, Texas, United States
- Pfizer Investigational Site
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Utah
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Salt Lake City, Utah, United States
- Pfizer Investigational Site
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Vermont
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Woodstock, Vermont, United States
- Pfizer Investigational Site
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Virginia
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Virginia Beach, Virginia, United States
- Pfizer Investigational Site
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Washington
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Everett, Washington, United States
- Pfizer Investigational Site
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Spokane, Washington, United States
- Pfizer Investigational Site
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Tacoma, Washington, United States
- Pfizer Investigational Site
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Wisconsin
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Milwaukee, Wisconsin, United States
- Pfizer Investigational Site
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients must meet the ACR criteria for fibromyalgia (ie, widespread pain present for at least 3 months, and pain in at least 11 of 18 specific tender point sites.
- Patients must complete the double-blind study.
Exclusion Criteria:
- Patients who experienced a serious adverse event during the previous fibromyalgia study, which was determined to be related to the study medication.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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To evaluate the safety of pregabalin in patients with fibromyalgia
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2006
Study Completion (Actual)
October 1, 2006
Study Registration Dates
First Submitted
January 26, 2006
First Submitted That Met QC Criteria
January 26, 2006
First Posted (Estimate)
January 27, 2006
Study Record Updates
Last Update Posted (Actual)
January 22, 2021
Last Update Submitted That Met QC Criteria
January 21, 2021
Last Verified
October 1, 2007
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Nervous System Diseases
- Musculoskeletal Diseases
- Rheumatic Diseases
- Muscular Diseases
- Neuromuscular Diseases
- Fibromyalgia
- Myofascial Pain Syndromes
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Central Nervous System Depressants
- Peripheral Nervous System Agents
- Analgesics
- Sensory System Agents
- Tranquilizing Agents
- Psychotropic Drugs
- Membrane Transport Modulators
- Anti-Anxiety Agents
- Anticonvulsants
- Calcium-Regulating Hormones and Agents
- Calcium Channel Blockers
- Pregabalin
Other Study ID Numbers
- A0081078
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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