Management of pain in abdominal laparoscopic surgery
Conditions
Interventions
Control group:Nil
QLB group:Unilateral or bilateral single quadratus lumborum block before anesthesia induction
ESPB group:Unilateral or bilateral single erector spinae plane block before anesthesia induction, PCIA concentration halved after operation
Sponsors
Drum Tower Hospital, Medical College of Nanjing University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Willing to participate in this study and sign informed consent; ASA physical condition I-III; aged 18-65 years; abdominal laparoscopic surgery (operation time > 2 hours).
Exclusion criteria
Exclusion criteria: 1. The subjects and their families refused to complete the clinical study; 2. They were known to be allergic to the study drug; 3. Chronic opioid use; 4. Epilepsy, mental retardation; 5. Morbid obesity (BMI > 40); 6. Serious cardiovascular adverse events occurred during the operation; 7. Other serious adverse events occurred after the operation, such as septic shock, acute renal failure, etc.; 8. When the doctor or researcher violated the principle of research design in the process of clinical research, the ethics committee terminated or suspended the clinical research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| The time of first postoperative analgesia ;Hemodynamic parameters during operation;The first time of activity;Time for dieting;Postoperative nausea and vomiting;Time for anal exhaust;days of hospital stay;Postoperative analgesic dosage; | — |
Countries
China
Contacts
Public ContactBingbing Li
Drum Tower Hospital, Medical College of Nanjing University
Outcome results
None listed