Monocentric Observational Study: Postoperative Pain After Cesarean Section: Incidence and Risk Factors.
CompletedNCT04280432
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
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)
Study details
- Official title
- Monocentric Observational Study: Postoperative Pain After Cesarean Section: Incidence and Risk Factors.
- Conditions
- Chronic Postoperative Pain
- Cesarean Section Complications
- Interventions
- Procedure: CESAREAN
- Sponsor
- Instituto de Investigación Hospital Universitario La Paz
- Start date
- 2017-03-01
- Primary completion
- 2018-09-30
- Sex
- Female
- Age range
- from 18 Years to 50 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Countries
- Spain
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
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
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04280432