Anesthesia; Adverse Effect, in Labor and Delivery Clinical Trial
Official title:
Incidence of Anesthesia-related Adverse Events and Obstetric Complications After Cesarean Delivery: a Retrospective Study
| NCT number | NCT03391648 |
| Other study ID # | 106116-E |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | January 1, 2018 |
| Est. completion date | December 31, 2018 |
| Verified date | February 2019 |
| Source | Far Eastern Memorial Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
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.
| Status | Completed |
| Enrollment | 505 |
| Est. completion date | December 31, 2018 |
| Est. primary completion date | December 31, 2018 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 20 Years and older |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| Taiwan | Far Eastern Memorial Hospital | New Taipei City |
| Lead Sponsor | Collaborator |
|---|---|
| Far Eastern Memorial Hospital |
Taiwan,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Incidence of anesthesia-related adverse events | Within 42 days after delivery |