Gall bladder stone, Cholecystitis
Conditions
Interventions
Experimental group (EOIB combined with general anesthesia) :None
Control group (TAP block combined with general anesthesia):None
Sponsors
ZhangZhou Municipal Hospital of Fujian province
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Age 18–75 years, no gender restriction; 2. ASA I–III; 3. Intended to undergo laparoscopic cholecystectomy; 4. Understand and consent to participate in the study by signing a written informed consent form; 5. Able to comprehend and cooperate with postoperative pain scoring and scale assessments.
Exclusion criteria
Exclusion criteria: 1. Allergy to local anesthetics or study-related medications; 2. Uncontrolled infection at the puncture site, abdominal skin defect, or systemic infection; 3. Coagulation dysfunction (INR> 1.5 or platelet count <80×10?/L); 4. Severe cardiopulmonary or hepatic/renal dysfunction, chronic obstructive pulmonary disease; 5. History of chronic pain or use of opioid analgesics within 2 weeks prior to surgery; 6. Mental illness or cognitive impairment preventing cooperation with pain assessment; 7. Pregnant or breastfeeding women; 8. Other medical or non-medical conditions deemed by the investigator as unsuitable for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative 24-hour resting VSA; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative 24-hour dosage and utilization rate of rescue analgesics;Visual simulation scoring during the activity;Quick recovery indicators: time to first flatus postoperatively, time to first ambulation postoperatively, postoperative hospital stay duration;Duration of analgesia;Postoperative patient satisfaction score for analgesia; | — |
Countries
China
Contacts
Public ContactJiang Liwei
ZhangZhou Municipal Hospital of Fujian province
Outcome results
None listed