postoperative pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age 18~80 years old; 2) ASA Grading I.~III. 3) Patients undergoing elective thoracoscopic lobe surgery
Exclusion criteria
Exclusion criteria: 1) Contraindications to transcranial electrical stimulation (implantation of electronic devices (such as pacemakers or other metal devices) in the body, cavities or cracks in the skull, or local skin damage or inflammation); 2) Pregnant and lactating women; 3) History of neurosurgery, epilepsy or psychiatric disorders; 4) Patients with a history of chronic pain or long-term use of analgesic and sedative drugs, or alcohol abuse; 5) Those with obvious impairment of liver and kidney function; 6) BMI=40kg/m2; 7) History of long-term use of anticoagulant drugs, abnormal blood coagulation; 8) Patients who are allergic to the drugs required in the study or refuse to use the intravenous self-controlled analgesic pump; 9) Patients who refuse to sign the informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 24-hour cumulative morphine consumption equivalent;Postoperative pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of recovery score postoperatively;Adverse effects;48-hour cumulative morphine consumption equivalent; | — |
Countries
China
Contacts
The First Affiliated Hospital of Zhengzhou University