None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Singleton live fetus at 37 to 41+6 weeks of gestation; 2.Elective cesarean section; 3.Both the pregnant woman and her spouse have provided informed consent to participate in the study; 4.Individuals with waived informed consent (for the control group);
Exclusion criteria
Exclusion criteria: 1.Pregnant women with severe pre-operative comorbidities or complications (e.g., pregnancy complicated by severe heart disease, eclampsia, complete placenta previa, or unstable vital signs); 2.Pregnant women for whom neonatal transfer to another department for treatment after birth is pre-operatively confirmed; 3.Multiple pregnancies (twins or more); 4.Pregnant women or their spouses request withdrawal from the study;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effective EENC implementation rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative satisfaction of cesarean section puerpera;Healthcare provider satisfaction;Postpartum hemorrhage volume of puerpera (hemoglobin method);Breastfeeding rate within the "golden 1 hour"; | — |
Countries
China
Contacts
The University of Hongkong - Shenzhen Hospital