Gastrointestinal surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients scheduled for elective gastrointestinal surgery; 2) ASA I-II level; 3) Age 18-65 years; 4) Surgery duration of 2-4 hours; 5) Willing to receive lidocaine intravenously, informed and willing to participate in this study, and voluntarily sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1) Allergy or contraindications to lidocaine; 2) conduction block arrhythmia, sinus bradycardia, preexcitation syndrome, AS syndrome, atrial fibrillation, etc.; 3) Severe hepatic and renal dysfunction; 4) Serious mental illness, such as schizophrenia, depression, dementia, etc.; 5) Neuromuscular diseases; 6) Patients with difficult airway; 7) Pregnant women; weight 100kg; 8) History of chronic analgesics, long-term history of opioid drugs, alcohol or medication Abuse of things; 9) Taking other trial drugs three months before the study, participated in or are participating in other clinical trials; 10) Unable to cooperate with the study for any reason or the investigator considers unsuitable for inclusion in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Protein levels; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pain VAS score;Postoperative inflammatory markers after 48 hours; | — |
Countries
China
Contacts
Anesthesiology Department of Sichuan Provincial People's Hospital