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Effect of esketamine combined with lidocaine on opioid demand in colorectal cancer surgery under general anesthesiaEffect of esketamine combined with lidocaine on opioid demand in colorectal cancer surgery under general anesthesia

Effect of esketamine combined with lidocaine on opioid demand in colorectal cancer surgery under general anesthesiaEffect of esketamine combined with lidocaine on opioid demand in colorectal cancer surgery under general anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078997
Enrollment
Unknown
Registered
2023-12-22
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal cancer

Interventions

Esketamine group:Esketamine 0.1mg/kg was slowly pushed before incision, and then esketamine 0.12mg·kg-1·h-1 was continuously pumped intravenically until the end of surgery
Lidocaine group:Lidocaine was given 2 mg/kg slow infusion before incision, followed by lidocaine 1.5 mg·kg-1·h-1 continuous intravenous pump until the end of surgery
Lidocaine and Esketamine group:Before incision, lidocaine 2mg /kg+ esketamine 0.1mg/kg was slowly injected, and then lidocaine 1.5 mg·kg-1·h-1 and esketamine 0.12mg·kg-1·h-1 were continuously pumped i
Control group:The same amount of normal saline was given before and during the operation

Sponsors

Xiangyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Age =60 years old; ASA Grade I - III; Laparoscopic radical resection of colorectal cancer under quasi-general anesthesia; No previous history of allergy to narcotic drugs; Sign the informed consent form.

Exclusion criteria

Exclusion criteria: Previous history of neuropsychiatric diseases such as cerebrovascular disease, Parkinson's disease, Alzheimer's disease, schizophrenia, etc. Currently using sedatives or antidepressants, etc.; Severe heart block or grade ? to ? heart function, uncontrolled hypertension, abnormal liver and kidney function; History of emergency surgery for colorectal cancer obstruction or perforation; Tumor invasion of adjacent vital tissues and organs; Obesity, extensive intraperitoneal adhesion, coagulation dysfunction; Preoperative cognitive dysfunction; Those who cannot cooperate to complete the cognitive function test; Persons with contraindications to esketamine and/or lidocaine; Other conditions determined by the investigator to be inappropriate for participation in this clinical trial.

Design outcomes

Primary

MeasureTime frame
VAS pain score;Ramsay calm score;

Secondary

MeasureTime frame
Opioid consumption;Length of stay;

Countries

China

Contacts

Public ContactLiwen Zhou

Xiangyang Central Hospital

462752149@qq.com+86 139 7228 7559

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026