Postoperative Pain
Conditions
Interventions
S-Group:single nerve block
C-Group:Combined nerve block
Sponsors
Shanghai General Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1)Age>18 years 2)Scheduled for elective thoracoscopic pulmonary resection surgery for the first time 3)American Society of Anesthesiologists(ASA) physical status I-III 4)Inform the relevant contents of this clinical trial and sign the informed consent
Exclusion criteria
Exclusion criteria: 1) Combination of severe cardiopulmonary, hepatic, or renal dysfunction 2) Allergy to bupivacaine liposome 3) Preoperative coagulation dysfunction 4) History of mental illness 5) Inability to understand visual analog scores(VAS)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative Pain; | — |
Secondary
| Measure | Time frame |
|---|---|
| 48-hour postoperative sufentanil consumption;Number of PCA demands;Intraoperative opioid consumption;endotracheal extubation time in the recovery room;length of postoperative hospitalization;Quality of postoperative recovery;postoperative complications; | — |
Countries
China
Contacts
Public ContactTang Lijun
Shanghai General Hospital
Outcome results
None listed