Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07359170

Delivery Mode Impact on Postoperative Depression

Impact of Elective Versus Emergency Cesarean Delivery on Early Postpartum Depression: a Retrospective Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
4,000 (estimated)
Sponsor
Jingping Wang, MD, Ph.D. · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational retrospective cohort study is to examine the association between mode of delivery and early postpartum depressive symptoms in adult women who delivered at Massachusetts General Hospital. Specifically, the study evaluates whether the urgency of cesarean delivery (elective versus emergency) is associated with differences in Edinburgh Postnatal Depression Scale (EPDS) scores at 6-8 weeks postpartum, compared with elective cesarean delivery and vaginal delivery. The EPDS is a validated 10-item self-report questionnaire with scores ranging from 0 to 30, where higher scores indicate more severe depressive symptoms. The primary questions are whether EPDS scores differ among women undergoing emergency cesarean delivery, elective cesarean delivery, and vaginal delivery, and whether perioperative and obstetric factors are associated with postpartum depressive symptoms. This study involves retrospective analysis of de-identified electronic health record data. Participants will not undergo any study-specific interventions.

Conditions

Timeline

Start date
2026-01-15
Primary completion
2026-02-28
Completion
2026-02-28
First posted
2026-01-22
Last updated
2026-01-23

Source: ClinicalTrials.gov record NCT07359170. Inclusion in this directory is not an endorsement.