Postoperative acute pain
Conditions
Interventions
Experimental group:0.4%ropivacaine for bilateral T7 level block
Control group:0.9% NaCl for bilateral T7 level block
Sponsors
The First Medical Center of PLA General Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Aged over 18 years old; 2. Patients scheduled to undergo open hepatobiliary surgery under general anesthesia; 3. Patients agreed to participate in the clinical study and signed informed consent.
Exclusion criteria
Exclusion criteria: 1. Emergency operation; 2. Patients with history of chronic pain before operation; 3. BMI>30 4. Patients with local infection or rash at the puncture site; 5. Patients with severe abnormal liver, renal function or coagulation function; 6. Patients who participated in other drug trials in the last 6 months; 7. Known allergic reactions to the test drug and / or its components; 8. The patients who were judged to lack the ability of informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric rating scales; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative complications; | — |
Countries
China
Contacts
Public ContactLiu Yanhong
The first medical center of PLA General Hospital
Outcome results
None listed