A prospectve observational study of maternal and umbilical blood anesthetic concentration and neonatal health status in the case of conversion from epidural labor analgesia to cesarean section.
Not Applicable
Recruiting
- Conditions
- Mother and her baby who undergo cesarean secion using epidural catheter for labor analgesia
- Registration Number
- JPRN-UMIN000051325
- Lead Sponsor
- ational center for child health and development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 1000
Inclusion Criteria
Not provided
Exclusion Criteria
Pregnant women with congenital anomalies in the fetus. Pregnant women with fetal growth restriction.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method We asses the neonatal health status immediately after birth. The neonatal health status includes Apgar score, umbilical cord artery blood pH, neonatal resuscitation, and admission to the NICU/GCU.
- Secondary Outcome Measures
Name Time Method We evaluate the condition of the mother from the beginning of anesthetic administration for cesarean section to the end of cesarean section. We evaluate the presence of local anesthetic systemic toxicity and respiratory depression as a maternal condition.