Postoperative analgesia
Conditions
Interventions
Experimental group:Compound betamethasone combined with ropivacaine erector spinae plane block
Control group:Ropivacaine alone erector spinae plane block
Sponsors
Yan'an Hospital of Kunming City
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age= 18 years old, gender is not limited; 2. ASA grading I.~III. 3. Patients who are scheduled to undergo elective thoracoscopic unilateral partial lung resection; 4. Those who voluntarily join this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Pregnant or lactating patients; 2. Those who are allergic to compound betamethasone, ropivacaine or other anesthetic drugs; 3. Patients with severe coagulation disorders and risk of bleeding; 4. Patients receiving chemotherapy and hormone therapy; 5. Patients with a history of spinal surgery, infection or cancer at the puncture site; 6. History of abuse of alcohol, opioids or other psychotropic substances; 7. Patients who cannot cooperate with the study due to language comprehension disorders, hearing impairments, mental illnesses, etc.; 8. Patients who are scheduled to be transferred to the intensive care unit (ICU) before surgery; 9. Patients who have participated in other studies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of moderate to severe pain in 24 hours after surgery;Postoperative recovery quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence and severity of nausea and vomiting at 24 and 48 hours after surgery were carried out; | — |
Countries
China
Contacts
Public ContactLiu Linfen
Yan'an Hospital of Kunming
Outcome results
None listed