Postoperative pain
Conditions
Interventions
Experimental group :Bupivacaine liposome combined with bupivacaine hydrochloride
Control group:Bupivacaine hydrochloride
Sponsors
Beijing Chao-Yang Hospital, Capital Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Patients undergoing elective thoracoscopic lobectomy/segment resection under general anesthesia; 2. Age 18-70 years old; 3.BMI18-30 kg /m^2; 4. ASA Grading I.-III.
Exclusion criteria
Exclusion criteria: 1.BMI>=30kg/m^2; 2. Presence of contraindications to thoracic paravertebral nerve block; 3. Combined with severe arrhythmia or circulatory system disease, poor liver and kidney function, respiratory system and coagulation system dysfunction; 4. Have communication disorders and are unable to complete the relevant scores normally; 5. I or my authorized person do not accept the plan.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total opioid consumption in 72 hours after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| Resting NRS score;Active NRS score;PCIA first compression time;Postoperative rescue analgesia times;Postoperative Quality of Recovery Score (QoR-15);Incidence of adverse events; | — |
Countries
China
Contacts
Public ContactAnshi Wu
Beijing Chao-Yang Hospital, Capital Medical University
Outcome results
None listed