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

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03391648

Enrollment

505

Registered

2018-01-05

Start date

2018-01-01

Completion date

2018-12-31

Last updated

2019-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia; Adverse Effect, in Labor and Delivery

Brief 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.

Interventions

OTHERObservation

Observation only

Study design

Observational model

OTHER

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Incidence of anesthesia-related adverse events	Within 42 days after delivery

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026