CompletedNot Applicable

Monocentric Observational Study: Postoperative Pain After Cesarean Section: Incidence and Risk Factors.

Spain610 participantsStarted 2017-03-01

Plain-language summary

The purpose of this prospective study was to assess chronic pain 3, and 12 months after cesarean delivery in a cohort of women in University hospital La Paz. We also aim to study the possible contribution of anesthetic and surgical risk factors for the development of Chronic post-surgical pain after cesarean (PCSCP)

Who can participate

Age range18 Years – 50 Years

SexFEMALE

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Inclusion Criteria: * Anesthesiologists scale (ASA) had to be I, II or III Exclusion Criteria: * history of major psychiatric disorder and inability to undertake a personal or telephone interview, ASA\> III or dead fetus as result of caesarean section

What they're measuring

assess if clinically relevant pain measured by neuropathic pain questionnaire of 2 questions (DN2) > 3/10 one week after cesarean section(CS) was a risk factor for chronic post-surgical pain (CPSP)

Timeframe: three months

Trial details

NCT IDNCT04280432

SponsorInstituto de Investigación Hospital Universitario La Paz

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-09-30

View on ClinicalTrials.gov More Chronic Postoperative Pain trials