Study of Paxil Use in Menopausal Women

PHASE4CompletedINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

September 30, 2004

Study Completion Date

September 30, 2006

Conditions
Menopause
Interventions
DRUG

Paroxetine

Paroxetine CR 12.5 mg/day; dosing may be adjusted up to 25 mg/day after two weeks, based on treatment response and tolerability

DRUG

placebo

Subjects enter into a six-week, double blind phase, randomized in a 1:1 ratio to paroxetine CR 12.5 mg/day or matching placebo pill; dosing may be adjusted up to 25 mg/day after two weeks, based on treatment response and tolerability.

Trial Locations (1)

02116

MGH Center for Perinatal and Women's Mental Health, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Massachusetts General Hospital

OTHER