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C-Section urgency linked to postpartum depression risk?

NCT ID NCT07359170

Knowledge-focused Sponsor: Jingping Wang, MD, Ph.D. Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether having a planned (elective) or unplanned (emergency) C-section affects a mother's risk of early postpartum depression. Researchers will review medical records of 4,000 women who gave birth at Massachusetts General Hospital. They will compare depression screening scores from 6-8 weeks after delivery to see if the type of delivery matters.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 4,000 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

adult patients (≥18 years old) who underwent cesarean delivery or vaginal delivery

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Underwent cesarean delivery (elective or emergency) or vaginal delivery during the study period Age 18 years or older Completed at least one Edinburgh Postnatal Depression Scale (EPDS) assessment at 6-8 weeks postpartum Have complete perioperative data available Exclusion Criteria: Missing 6-8 week postpartum EPDS scores Pregnancy with fetal demise, severe obstetric complications, or atypical maternal conditions History of severe psychiatric disorders (e.g., schizophrenia, bipolar disorder), when identifiable Incomplete perioperative medical records

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Postoperative depression

How to take part

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  1. The official record

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    Open the record ↗

  2. A doctor treating you

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