Cesarean section Cesarean section
Conditions
Interventions
Intervention begins when the onset of labor pains occurs. Propofol is administered using a TCI (Targeted Controlled Infusion
TCI) pump, and the blood concentration is gradually increased, with the effect-site concentration set as the target blood concentration when sufficient sedation is achieved. Dexmedetomidine is admini
D000771
Sponsors
Kii Natsumi
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients aged 18 years or older who are undergoing Caesarean section after the 38th week of pregnancy and will receive sedatives after delivery
Exclusion criteria
Exclusion criteria: Patients under 18 years of age, under 37 weeks pregnant, patients with a history of allergies to propofol, dexmedetomidine, or fentanyl, patients with contraindications for propofol or dexmedetomidine, or patients who did not give their consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The endpoint was recovery status from day 1 to day 5 after surgery using the postpartum recovery score ObsQoR. | — |
Secondary
| Measure | Time frame |
|---|---|
| Screening for the onset of postpartum depression was performed using the Edinburg Postnatal Depression Scale (EPDS), a postpartum depression scale. BDNF levels before anesthesia induction after entering the operating room and on the first postoperative day, additional postoperative analgesic dosage, time to mobilization after surgery, length of hospital stay, pain score (Numeric Rating Scale; NRS), and the presence or absence of complications were also assessed. | — |
Contacts
Public ContactNatsumi Kii
Sapporo Medical University
Outcome results
None listed