7
Participants
Start Date
February 28, 2007
Primary Completion Date
June 30, 2008
Study Completion Date
June 30, 2008
Duloxetine
During the current study, for a short period of time participants will receive a placebo (a pill that looks like the study drug but which does not contain any medication), although during the majority of the study, participants will be receiving the actual study medication (Duloxetine). The initial dose of Duloxetine to be given will be a 30 mg dose with the dosage increased over time to 60 mg per day. This study will be blinded, meaning that participants will not know whether they are taking placebo or the study drug. However, all subjects will receive duloxetine for the majority of the time they are enrolled in the trial. Investigators will know when subjects are receiving the placebo but in order to maintain the blinding of this study, the study staff will not be able to tell participants when they are taking placebo and when they are taking Duloxetine.
Women's Mental Health Program; University of Arizona; Department of Psychiatry, Tucson
Eli Lilly and Company
INDUSTRY
University of Arizona
OTHER