Cesarean section
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteer to participate in this experiment, aged 20-40 years old; Pregnant women with a single full-term fetus (gestational age >=37 weeks) scheduled for elective lower segment cesarean section; ASA class II; BMI 18.5–35 kg/m²; normal liver and kidney function and coagulation function; able to independently complete questionnaires and use PCIA; signed informed consent.
Exclusion criteria
Exclusion criteria: Contraindications for regional block/spinal anesthesia; allergy to study medications (ropivacaine, sufentanil); poorly controlled gestational diabetes, liver or kidney dysfunction; complicated by preeclampsia/eclampsia/HELLP syndrome; history of chronic pain or long-term use of analgesics and sedatives; cognitive impairment or psychiatric disorders;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total 24-hour consumption of sufentanil;Time of first use of rescue analgesia after surgery;Pain relief satisfaction;Quality of Recovery; | — |
Countries
China
Contacts
The Second Affiliated Hospital of Shandong First Medical University