Status:

COMPLETED

Postpartum Depression and Cesarean Section

Lead Sponsor:

Oklahoma State University Center for Health Sciences

Conditions:

Postpartum Depression

Eligibility:

FEMALE

15-43 years

Brief Summary

The purpose of this retrospective study is to determine if there is an increase in postpartum depression (PPD) among women who undergo an emergency cesarean section as opposed to a planned cesarean se...

Detailed Description

The purpose of this retrospective study is to determine if there is an increase in postpartum depression (PPD) among women who undergo an emergency cesarean section as opposed to a planned cesarean se...

Eligibility Criteria

Inclusion

  • Included are postpartum women ages 15 to 43 who have given birth via cesarean section at Tulsa Regional Medical Center between January 1, 2003 and June 1, 2005. Postpartum follow up visit(s) must have occurred at the OSU Ob/Gyn Clinic in Tulsa, Oklahoma.

Exclusion

  • Patients who deliver vaginally, have an intrauterine fetal demise, known anomalies in the delivered fetus, a known mood disorder during pregnancy, or drug use during pregnancy or the postpartum course will be excluded.

Key Trial Info

Start Date :

August 1 2006

Trial Type :

OBSERVATIONAL

End Date :

November 1 2007

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT00370903

Start Date

August 1 2006

End Date

November 1 2007

Last Update

February 4 2008

Active Locations (1)

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Oklahoma State University Center for Health Sciences Houston Parke Clinic

Tulsa, Oklahoma, United States, 74127