A Study Evaluating Desvenlafaxine Sustained Release (DVS SR) in Adult Female Outpatients With Fibromyalgia

Stopped early · Phase 2 · Has a placebo group

Conditions studied: Fibromyalgia

In brief

The purpose of this study is to evaluate if DVS SR is safe and effective in the treatment of pain associated with fibromyalgia syndrome, and if so to identify the efficacious doses.

Key facts

Study ID

NCT00696787

Run by

Wyeth is now a wholly owned subsidiary of Pfizer

People needed

125

Starts

2008-06-01

Expected to finish

2009-01-01

Last updated by the study team

2013-02-25

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Fibromyalgia diagnosed according to 1990 American College of Rheumatology criteria

You may not qualify if…

• Unstable medical or psychological conditions that would compromise the subject's safety or put the subject at greater risk during study participation
• Other painful conditions that may confound the diagnosis or assessment of fibromyalgia
• Treatment with other drugs for fibromyalgia with 14 days of study start or during the study

Where it is running

• Study site — Huntsville, Alabama, United States
• Study site — Roseville, California, United States
• Study site — San Diego, California, United States
• Study site — San Diego, California, United States
• Study site — Santa Ana, California, United States
• Study site — Walnut Creek, California, United States
• Study site — Jacksonville, Florida, United States
• Study site — Tampa, Florida, United States
• Study site — Decatur, Georgia, United States
• Study site — Evansville, Indiana, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Lexington, Kentucky, United States
• Study site — Rockville, Maryland, United States
• Study site — Lansing, Michigan, United States
• Study site — Raleigh, North Carolina, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Dayton, Ohio, United States
• Study site — Duncansville, Pennsylvania, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Chattanooga, Tennessee, United States
• Study site — Chattanooga, Tennessee, United States
• Study site — Knoxville, Tennessee, United States
• Study site — Austin, Texas, United States
• Study site — Dallas, Texas, United States
• Study site — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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