Can a simple recovery plan prevent chronic pain after C-Sections?
NCT ID NCT04919408
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
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.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for CHRONIC POST-CESAREAN PAIN are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Centre Hospitalier Intercommunal Toulon La Seyne sur Mer
Toulon, 83056, France
-
Hôpital Nord
Marseille, Bouches-du-Rhône, 13915, France