None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Pregnant women with a body mass index (BMI) = 30 kg/m² at the time of delivery Pregnant women with a singleton pregnancy Pregnant women at a gestational age of = 36 weeks Pregnant women scheduled for elective cesarean section Pregnant women classified as American Society of Anesthesiologists (ASA) physical status II–III Pregnant women who have received sufficient explanation of the study objectives, procedures, potential risks, and benefits, and have voluntarily provided written informed consent
Exclusion criteria
Exclusion criteria: Pregnant women who did not provide written informed consent or who withdrew consent Pregnant women with a multiple pregnancy Pregnant women with a gestational age of less than 36 weeks Pregnant women with a history of hypersensitivity or allergic reactions to anesthetic agents or related medications used in the study Pregnant women who were deemed inappropriate for study participation or data analysis based on the investigator’s clinical judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time from skin incision to umbilical cord clamping (seconds) | — |
Secondary
| Measure | Time frame |
|---|---|
| Surgical difficulty score;total operation time;estimated blood loss;maternal anesthetic and hemodynamic variables (intubation time, incidence of hypoxemia and hypotension);maternal and umbilical cord blood gas analysis results;neonatal Apgar scores at 1 and 5 minutes | — |
Countries
Korea, Republic of
Contacts
Chonnam National University Hospital