Paroxetine-CR (Paxil-CR) in the Treatment of Patients With Fibromyalgia Syndrome

PHASE4CompletedINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

January 31, 2002

Primary Completion Date

December 31, 2002

Study Completion Date

December 31, 2002

Conditions
Fibromyalgia Syndrome
Interventions
DRUG

Paroxetine CR

Those in the active treatment group will receive doses of Paxil CR in the following manner: week 1: 12.5 mg per day, week 2: 25 mg per day, week 3: 37.5 mg per day, wk 4: 50 mg per day and week 5: 62.5 mg per day.

DRUG

Placebo

Same shape Placebo

Trial Locations (2)

19107

Thomas Jefferson University, Philadelphia

27705

Duke University Medical Center, Durham

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Duke University

OTHER