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Can a simple recovery plan prevent chronic pain after C-Sections?

NCT ID NCT04919408

Knowledge-focused Sponsor: Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jul 08, 2026 · Updated 3 times

Summary

This completed study surveyed 283 women who had scheduled C-sections under spinal anesthesia and followed an Enhanced Recovery After Surgery (ERAS) protocol. Researchers called participants at 3 and 6 months to ask about scar pain and how it affected daily life. The goal was to see how common chronic pain is with this approach and whether the ERAS protocol helps prevent it.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this study could show that the ERAS protocol reduces chronic pain after C-sections, leading to better recovery guidelines.
What could go wrong
This is an observational survey, not a treatment trial. Results may not prove cause and effect, and the sample is limited to scheduled C-sections under spinal anesthesia.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

283 people

The number who actually took part.

Started

Jul 2021

Finished

Aug 2024

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.

Ages

18 to 55 years

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: * Patients scheduled for cesarean section under spinal anesthesia * Patients ASA I and II according to The ASA Physical Status Classification System Exclusion Criteria: intervention under general anesthesia * complication during the operation * post-partum haemorrrhage * pre-op anemia \<9g / dl * Patient under judicial protection (guardianship, curatorship...) or safeguard of justice. * Patient unable to answer the questionnaires by telephone (not speaking French, hard of hearing, mute French language, hearing impaired, mute...) * Any other reason that, in the opinion of the investigator, could interfere with the evaluation of the objectives of the study

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Conditions

The condition(s) this trial relates to.

Chronic Pain

As listed by the trial registrant

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

Chronic post cesarean pain

Contacts and locations

Locations

  • Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

    Toulon, 83056, France

  • Hôpital Nord

    Marseille, Bouches-du-Rhône, 13915, France

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