Clinical Trial

Delivery Mode Impact on Postoperative Depression

Not Yet Recruiting
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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.
Protocol Amendment History 2 changes
notable Primary completion pushed: 2026-02-28 -> 2027-10-28 2026-06-10
minor Completion pushed: 2026-02-28 -> 2027-12-28 2026-06-10
Trial Details
NCT Number NCT07359170
Lead Sponsor Jingping Wang, MD, Ph.D.
Conditions Postoperative Depression
Enrollment 4,000 participants
Start Date 2026-10-15
Primary Completion 2027-10-28 (estimated)
Study Completion 2027-12-28 (estimated)
Updated on ClinicalTrials.gov 2026-06-09