New study tracks why some women have lasting pain after C-Section
NCT ID NCT06247852
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This completed study followed 477 women in Denmark who had a planned cesarean delivery. Researchers used text-message surveys to track pain levels, medication use, and how pain affected daily life over several months. The goal was to better understand how common persistent pain is after C-section and how it relates to early post-surgery pain.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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477 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Sep 2025
- Lead sponsor
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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
Patients, aged \> 18 years, who undergo planned cesarean delivery under spinal anesthesia.
- Ages
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18 years and older
- Sex
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Female participants only
Show the full entry requirements Hide 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 who, after participating in the Danish multicenter cohort study on pain after cesarean delivery (ClinicalTrials.gov Identifier: NCT06012747), consent to continue to receive questionnaires about persistent pain. * Planned cesarean delivery in spinal anesthesia * Patients who speak and read Danish * Patients with a smartphone that can receive an SMS with a link to a questionnaire that can be opened online. Exclusion Criteria: • \<18 years of age
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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
Locations
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Department of Anesthesiology, Copenhagen University Hospital, North Zealand Hillerød
Hillerød, 3400, Denmark
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Other studies related to the condition(s) this trial covers.
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