Sleep quality
Conditions
Interventions
Test group:A small dose of esketamine (0.2mg/kg) was administered intravenously after delivery of the severed umbilicus
Control group:The patient was injected intravenously with 0.9% sodium chloride injection of equal volume after delivery of the severed umbilicus
Sponsors
Chengdu Pidu District maternal and Child Health Care Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. American Society of Anesthesiologists (ASA) grade I, IIPatients undergoing cesarean section under combined spinal and epidural anesthesia; 2. Age over 20 years old, less than 40 years old; 3. Preoperative routine examination was normal; 4. Intravenous analgesia and transversal plane block were used after cesarean section.
Exclusion criteria
Exclusion criteria: 1. The patient was exposed to any of the drug ingredients in the study Sensitive or addicted; 2. Those who are unwilling to cooperate; 3. Patients with gestational hypertension, preeclampsia, eclampsia and other pregnancy complications or other underlying diseases; 4. can not accurately understand the visual analog scale (VAS), Pittsburgh Sleep Quality Index (PSQI), Edinburgh Postpartum Depression Scale (EPDS), insomnia Severity Index (ISI) and other contents; 5. Pittsburgh Sleep Quality Index (PSQI) greater than 5 before surgery; 6. The end time of the operation is from 24:00 to 6AM; 7. Participants considered unsuitable for clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality;Visual analog score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Interleukin 18;C-reactive protein;Postoperative 24-hour salvage analgesia rate;Edinburgh Postnatal Depression Scale (EPDS) score; | — |
Countries
China
Contacts
Public ContactLiu Shushu
Chengdu Pidu District maternal and Child Health Care Hospital
Outcome results
None listed