Acute pain after thoracic surgery
Conditions
Interventions
Bupivacaine Liposome:None
Sponsors
Shanghai Pulmonary Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Understand the nature, significance, and possible benefits of the trial in detail before the trial, be able to understand the procedures and methods of this study, be willing to strictly abide by the clinical trial protocol to complete the trial, and voluntarily sign the informed consent form; 2. Elective thoracic surgery; 3. Age>=18 years old; 4. American Society of Anesthesiologists (ASA) grade I.~III.; 5. Patients using bupivacaine liposomal injection.
Exclusion criteria
Exclusion criteria: 1. Patients with psychiatric diseases and cognitive dysfunction; 2. Patients with sensory impairments such as hyperalgesia, or other physical pain that affects postoperative pain assessment; 3. History of myocardial infarction or unstable angina pectoris within half a year, or history of severe arrhythmia (if there is atrioventricular block of grade II or above); 4. Patients with diabetic peripheral neuropathy; 5. Known allergy to bupivacaine or other amide local anesthetics; 6. Pregnant and lactating patients, as well as female patients who have a birth plan within half a year and are unwilling or unable to take effective contraceptive measures; 7. Patients with any other factors that, in the opinion of the investigator, are not suitable for participation in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of severe pain; | — |
Countries
China
Contacts
Public ContactXin Lv
Shanghai Pulmonary Hospital
Outcome results
None listed