Postoperative pain
Conditions
Interventions
Experimental group:cheek acupuncture combined with local anesthetics incision infiltration
Control group:local anesthetics incision infiltration alone
Sponsors
First Affiliated Hospital of China Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1.Patients scheduled to undergo laparoscopic radical resection of colorectal cancer 2.Age ranging from 18 to 70 years at the time of enrollment 3.Body mass index (BMI) within the range of 18 to 24 kg/m^2 4.American Society of Anaesthesiologists (ASA) physical status class I to ? 5.Patients who learn about the trial in detail and sign the informed consent voluntarily
Exclusion criteria
Exclusion criteria: 1.Patients and their families patient refuse to participate in the study 2.Patients with abnormal coagulation function 3.Patients with infected or ulcerated skin at the acupuncture site 4.Patients with a history of chronic pain or continuous use of analgesics within 2 weeks before surgery 5.Patients with previous drug abuse or alcohol dependence 6.Patients who need to be transferred to the intensive care unit for treatment after surgery 7.Patients with psychiatric disorders, communication barriers, or taking psychiatric medications within the past 6 months. 8.Severe allergy to ropivacaine and other local anesthetic drugs 9. The responsible surgeon determines that the patient is unsuitable or poses medical risks for participation in the trial based on clinical assessment and judgment 10.Patients requiring conversion to open surgery or post-operative use of intravenous patient-controlled analgesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numerical score scale of postoperative pain at rest; | — |
Secondary
| Measure | Time frame |
|---|---|
| Numerical score scale of postoperative pain at rest;Numerical score scale of postoperative pain on motion;Sufentanil consumption during operation;Remifentanil consumption during operation;Time of first application of remedial analgesics;Times of remedial analgesia applied;Exhaustion (Y/N);mobility(0-2);Sleep satisfaction(0-2);Anxiety score(0-10);Postoperative nausea and vomiting (Y/N);Postoperative respiratory depression (Y/N);Postoperative fatigue (Y/N);Postoperative lethargy (Y/N); | — |
Countries
China
Contacts
Public ContactBao Naren
First Affiliated Hospital of China Medical University
Outcome results
None listed