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OpenTrials
Completed

NCT Number: NCT03391648

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

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.

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Key information

Conditions

Anesthesia; Adverse Effect, in Labor and Delivery

Age range

20 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Far Eastern Memorial Hospital

New Taipei City, 220, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all parturients underwent cesarean section at Far Eastern Memorial Hospital during 2012-2016

Exclusion criteria

  • missing data can't be collect during medical chart review

Treatment and study plan

observation

Other

Observation only

Primary outcomes

  1. Incidence of anesthesia-related adverse events

    Time frame: Within 42 days after delivery

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Official study title

Incidence of Anesthesia-related Adverse Events and Obstetric Complications After Cesarean Delivery: a Retrospective Study

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Jan 5, 2018
Registry last updated
Feb 15, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.