Antidepressant Treatment for Premenstrual Syndrome and Premenstrual Dysphoric Disorder

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

September 30, 2001

Primary Completion Date

June 30, 2007

Study Completion Date

January 31, 2008

Conditions
Premenstrual Syndrome
Interventions
DRUG

Sertraline

Patients who meet study criteria will be given 50 mg per day of sertraline to be taken an estimated 2 weeks before menstruation.

OTHER

Treatment as usual (TAU)

At the TAU baseline visit, patients will be told of their diagnosis of PMS/PMDD. Those patients who decide to seek treatment outside of the study protocol or do not wish to seek treatment will be asked to participate in the TAU part of this protocol. Patients in TAU will be contacted monthly to obtain monthly information about how they have been feeling (blinded ratings) using the study measures.

Trial Locations (1)

06510

Yale School of Medicine, New Haven

All Listed Sponsors
collaborator

National Institute of Mental Health (NIMH)

NIH

lead

Yale University

OTHER

NCT00048854 - Antidepressant Treatment for Premenstrual Syndrome and Premenstrual Dysphoric Disorder | Biotech Hunter | Biotech Hunter