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

NCT04280432 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 610

Last updated 2020-06-16

No results posted yet for this study

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)

Conditions

  • Chronic Postoperative Pain
  • Cesarean Section Complications

Interventions

PROCEDURE

CESAREAN

Women hospitalized for cesarean section

Sponsors & Collaborators

  • Instituto de Investigación Hospital Universitario La Paz

    lead OTHER

Principal Investigators

  • Maria Cristina R ROCA, FEA · Hospital Universitario La Paz

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-01
Primary Completion
2018-09-30
Completion
2018-09-30

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04280432 on ClinicalTrials.gov