Effect of Esketamine and Lidocaine on Postoperative Chronic Pain and Long-term Survival in Patients Undergoing Hepatectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorWest China Hospital

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

Treatment groups

304 Participants
are divided into 2 treatment groups

Sponsors and collaborators