Cesarean section
Conditions
Interventions
Bupivacaine liposome group:1.33% bupivacaine liposomal subcostal transversus abdominis fascia plane block, 20 ml each bilaterally
Bupivacaine group:0.25% bupivacaine for subcostal border transversus abdominis fascia plane block, 20 ml each bilaterally
Bupivacaine combined with dexamethasone and dexmedetomidine group:0.25% bupivacaine combined with 5mg dexamethasone and 30ug dexmedetomidine for subcostal transversus abdominis fascia planar block, 20
Sponsors
Gansu Maternal and Child Health Hospital (Gansu Provincial Center Hospital)
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: ASA classification II or III, signed informed consent. Age 18-45 years, singleton full-term pregnancy. Anesthesia was by lumbar anesthesia.
Exclusion criteria
Exclusion criteria: Those who refuse to sign the informed consent form. Those who are allergic to the study drug. Those with contraindications to lumbar anesthesia. Patients with previous history of abdominal surgery or chronic pain. Patients with a history of mental illness or inability to accurately express pain.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain scores at rest and during coughing at 2, 6, 12, 24, 48, and 72 hours postoperatively;Opioid Tramadol Dosage in the Postoperative Period of 72 Hours; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of postoperative injection site reactions, symptoms of local anesthetic toxicity and nausea, vomiting, sedation and other drug-related side effects associated with local anesthetics;Time to first postoperative bed mobility, duration of breastfeeding, and length of hospitalization; | — |
Countries
China
Contacts
Public ContactBao Yuncheng
Gansu Maternal and Child Health Hospital (Gansu Provincial Center Hospital)
Outcome results
None listed