Postoperative pain
Conditions
Interventions
Sponsors
Tianjin First Center Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Any gender, 18-65 years old; 2. Patients undergoing proposed abdominal surgery; 3. American Society of Anesthesiologists (ASA) physical status I to III; 4. Willing to sign an informed consent form, participate in the study, and complete all follow-up visits.
Exclusion criteria
Exclusion criteria: 1. History of allergy to local anesthetics; 2. Past history of dementia, psychosis, or other central nervous system disorders; 3. History of chronic pain or taking opioids and other analgesic drugs; 4. Contraindications to nerve block, including infection at the puncture site and severe coagulation disorders; 5. Chronic use of analgesic medications or known abuse of alcohol, drugs, or narcotics; 6. Concomitant with other conditions that may preclude enrollment, such as breastfeeding, pregnancy, neoplasia, and severe disability; 7. Those who refuse to participate or are unable to communicate; 8. Concurrent enrollment in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NRS score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Restore Quality Rating Sheet (QoR-15);Postoperative agitation score;Postoperative analgesic drug dosage;Postoperative adverse reaction incidence: nausea, vomiting, skin itching, allergic reactions;Time to extubate offline;Post-anesthesia care unit stay time; | — |
Countries
China
Contacts
Public ContactJia Lili
Department of Anesthesiology, Tianjin First Central Hospital
Outcome results
None listed