About this trial
This study is a further observation and follow-up of the patients enrolled in the registration number ChiCTR230007164430 to further evaluate the effect of long-term infusion of esketamine and lidocaine on postoperative chronic pain, long-term quality of life and survival rate in patients undergoing hepatectomy.
Eligibility criteria
Qualifiers
Aged 18-75 years;
Scheduled for elective hepatectomy;
ASA grade I-III.
Disqualifiers
Patients who have been intubated in the ICU following surgery and do not have a planned extubation within 6 hours postoperatively.
Patients with a body weight less than 40 kg or greater than 100 kg.
Patients with cardiac conduction system abnormalities (second- or third-degree atrioventricular block) or cardiac insufficiency (left ventricular ejection fraction < 50%).
Patients with severe hepatic insufficiency (alanine aminotransferase [ALT], aspartate aminotransferase [AST], or bilirubin levels more than 2.5 times the upper limit of normal) or renal insufficiency (creatinine clearance rate < 60 mL/min).
Trial design
Treatments tested in this trial
- Esketamine-lidocaine group
- Placebo group