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New french survey aims to improve cesarean birth experiences

NCT ID NCT07555353

Knowledge-focused Sponsor: University Hospital, Grenoble Source: ClinicalTrials.gov ↗

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 will translate an English survey that measures how satisfied women are after a cesarean section into French. Researchers will test the new French version with 210 women who had a planned or unplanned cesarean. The goal is to give hospitals a better tool to understand and improve care for mothers.

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 210 people

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

Expected to start

May 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

Patient who underwent a cesarean section under regional anesthesia at the Couple Enfant Hospital

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: * Patient on Day 1, Day 2, or Day 3 following a cesarean section performed under regional anesthesia at the Couple Enfant Hospital of the CHUGA * Patient of legal age at the time of the cesarean section Exclusion Criteria: * Patients who underwent a cesarean section under general anesthesia * Patients who underwent a cesarean section under deep sedation (this criterion will be verified by asking: "Do you remember your cesarean section?") * Patients who were placed on mechanical ventilation and/or under sedation in the intensive care unit following their cesarean section * Patient opposed to the use of her data for research purposes * Non-French-speaking patient * Patient who cannot read or write * Patient with cognitive or psychiatric disorders preventing her from understanding the questionnaire * Patient under legal guardianship or conservatorship, or deprived of liberty * Patient not enrolled in the social security system

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As listed by the trial registrant

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Post-cesarean maternal satisfaction scale

How to take part

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  1. The official record

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  2. A doctor treating you

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