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Therapeutic Areas: Rheumatology | Neurology | Musculoskeletal | Family Medicine
Disease Category: Fibromyalgia
Location: United States, OK

Clinical Trial Details

Overview

Research Study Summary

A Study for the Treatment of Subjects with Fibromyalgia

Purpose

This trial's participation duration is 21 weeks where subjects will be seen in the clinic for a total of 12 visits. Primary outcome is for a decrease in pain from fibromyalgia due to the study drug.

Patient Inclusion Criteria

  • Male or female subject must be 18 years of age or older and meets the ACR criteria for fibromyalgia.
  • Other inclusion criteria apply

Patient Exclusion Criteria

  • Subject has Major Depressive Disorder, Bipolar, or other psychotic disorder and cannot safely discontinue use of antidepressant medication.
  • Subject has Rheumatic disease in addition to fibromyalgia or other painful conditions that would interfere with the ability to measure change on any outcome measures associated with stiffness and muscle weakness.
  • Other exclusion criteria apply

Qualified participants will receive, at not charge, study medication, study-related medical care, and laboratory evaluations.

If you are interested in this, or any other studies we currently have enrolling, please contact us for further information.

To Learn more
Phase

3

Gender

Both Male and Female

Age

18 and up

Overall Status

Recruiting

Duration

21 Weeks

Facility Type

N/A

Contact

Rachel Waldrop, Director of Clinical Research
Health Research Institute
1044 S.W. 44th Street
Suite 403
Oklahoma City, OK 73109
Phone: 405-616-4888
Fax: 405-616-4885

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Research Center Information: Health Research Institute

If you would like to learn more about participating in this research study, please email the trial contact using the form below.

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CW ID: 107191

Date Last Changed: July 25, 2013


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