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Incidence of Anesthesia-related Adverse Events and Obstetric Complications After Cesarean Delivery

NCT03391648 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 505

Last updated 2019-02-15

No results posted yet for this study

Summary

Recruit the parturients who underwent cesarean delivery at Far Eastern MemorialHospital during 2012-2016. After reviewing medical record related to the pregnancy, demographic data, prenatal exam, laboratory data, indication for cesarean section, perioperative events, etc. will be recorded. Analysis will be focused on incidence, temporal trend, and risk factors of anesthesia-related adverse events and obstetric complications.

Conditions

  • Anesthesia; Adverse Effect, in Labor and Delivery

Interventions

OTHER

Observation

Observation only

Sponsors & Collaborators

  • Far Eastern Memorial Hospital

    lead OTHER

Eligibility

Min Age
20 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Taiwan

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 NCT03391648 on ClinicalTrials.gov