Uterine leiomyoma
Conditions
Interventions
conventional general anesthesia group (control group):Routine care protocols
Lidocaine group (experimental group):Intravenous infusion of lidocaine
Sponsors
The First People's Hospital of Zunyi
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Patients who consent to undergo gynecological surgery at a scheduled date; 2.Aged between 18 and 65 years, with an ASA classification of I-II; 3.Voluntarily participate in this study and sign the informed consent form;
Exclusion criteria
Exclusion criteria: 1.History of drug abuse or psychiatric disorders; 2.Patients who refuse to receive lidocaine infusion; 3.Use of psychotropic drugs or presence of psychological disorders; 4.BMI > 30 kg/m² or weight below 45 kg; 5.Allergy to any investigational drug; 6.Arrhythmias (such as sick sinus syndrome, Adams-Stokes syndrome, second- and third-degree atrioventricular block, bifascicular block, or heart rate < 50 beats/min); 7.Inability to complete the questionnaire due to language barriers or cognitive impairment; 8.Intraoperative drug toxicity or adverse reactions; 9.Patients requiring postoperative ICU monitoring or treatment;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative recovery quality of the patient; | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital signs and depth of anesthesia;Postoperative quality of life;Analgesic drug requirements;Postoperative pain score.;Postoperative anxiety and depressive status;Postoperative sleep status;Incidence of adverse react"; | — |
Countries
China
Contacts
Public ContactPan Changbin
The First People's Hospital of Zunyi
Outcome results
None listed