Study Evaluating Desvenlafaxine Succinate Sustained-release (DVS SR) in Adult Outpatients With Pain Associated With Diabetic Peripheral Neuropathy

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Diabetic Neuropathies, Pain

In brief

The purpose of this study is to evaluate the safety and efficacy of DVS SR in the treatment of neuropathic pain associated with diabetic peripheral neuropathy.

Key facts

Study ID

NCT00283842

Run by

Wyeth is now a wholly owned subsidiary of Pfizer

People needed

408

Starts

2006-03-01

Expected to finish

2008-06-01

Last updated by the study team

2011-10-24

Who can join

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

You may qualify if…

• Diabetes type 1 or 2
• Painful symptoms of diabetic neuropathy in the lower extremities extremities for at least 6 months

You may not qualify if…

• Major Depression
• Uncontrolled diabetes

Where it is running

• Study site — Peoria, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Encino, California, United States
• Study site — Newport Beach, California, United States
• Study site — Walnut Creek, California, United States
• Study site — Pueblo, Colorado, United States
• Study site — New Britain, Connecticut, United States
• Study site — Stratford, Connecticut, United States
• Study site — Waterbury, Connecticut, United States
• Study site — Fort Myers, Florida, United States
• Study site — Palm Beach Gardens, Florida, United States
• Study site — Pembroke Pines, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — West Palm Beach, Florida, United States
• Study site — Lawrenceville, Georgia, United States
• Study site — Roswell, Georgia, United States
• Study site — Coeur d'Alene, Idaho, United States
• Study site — Chicago, Illinois, United States
• Study site — Evansville, Indiana, United States
• Study site — Des Moines, Iowa, United States
• Study site — Madisonville, Kentucky, United States
• Study site — Springfield, Massachusetts, United States
• Study site — Ann Arbor, Michigan, United States
• Study site — Kansas City, Missouri, United States
• Study site — Mesa, Arizona, United States

Full record on ClinicalTrials.gov

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