Duloxetine for Perimenopausal Depression

PHASE4CompletedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

February 28, 2007

Primary Completion Date

June 30, 2008

Study Completion Date

June 30, 2008

Conditions
Major Depressive Disorder
Interventions
DRUG

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.

Trial Locations (1)

85724

Women's Mental Health Program; University of Arizona; Department of Psychiatry, Tucson

All Listed Sponsors
collaborator

Eli Lilly and Company

INDUSTRY

lead

University of Arizona

OTHER

NCT00517985 - Duloxetine for Perimenopausal Depression | Biotech Hunter | Biotech Hunter