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Clinical Study on the Effect of Esketamine on Postoperative High-Sensitivity Cardiac Troponin T/Troponin I Levels in Patients Undergoing Esophageal Cancer Resection Surgery

Clinical Study on the Effect of Esketamine on Postoperative High-Sensitivity Cardiac Troponin T/Troponin I Levels in Patients Undergoing Esophageal Cancer Resection Surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098877
Enrollment
Unknown
Registered
2025-03-14
Start date
2024-09-08
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

myocardial injury after non-cardiac surgery

Interventions

Group K:Anesthesia induction: midazolam 0.03mg/kg, etomidate 0.2mg/kg, cisatracurium benzoate 0.15mg/kg, Sufentanil 0.3-0.6µg/kg, esketamine 0.5mg/kg
Anesthesia maintenance: propofol 4-12mg/kg/h, remifentanil 0.1-1.0ug/kg/min, esketamine 0.25mg/kg/h, benzoate cisatracurium intermittent intravenous infusion to maintain good muscle relaxation
Group C:Anesthesia induction: midazolam 0.03mg/kg, etomidate 0.2mg/kg, cisatracurium benzoate 0.15mg/kg, Sufentanil 0.3-0.6µg/kg
Anesthesia maintenance: propofol 4-12mg/kg/h, remifentanil 0.1-1.0ug/kg/min, intermittent intravenous infusion of cisatracurium bensulate to maintain good muscle relaxation

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age>=45 years old 2.ASA grade II-III 3.BMI of 18.5-28.0kg/m^2 4.Radical resection of esophageal cancer should be performed at an appropriate time 5.No communication barriers, clear consciousness; 6.Ethical, voluntary test, signed informed consent

Exclusion criteria

Exclusion criteria: 1.There is contraindication or allergy to esketamine and other narcotic drugs 2.History of mental illness, central nervous system injury 3.Identified/suspected abuse or long-term use of narcotic sedatives and analgesics 4.A history of serious cardiovascular disease (e.g., myocardial infarction, heart failure) 5.Serious infection: such as sepsis 6.Severe liver and kidney function damage 7.Preoperative troponin I>30ug/ml 8.Refusal to sign informed consent

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative myocardial injury;

Secondary

MeasureTime frame
Perioperative hemodynamic changes;Perioperative blood gas analysis;Perioperative inflammatory factor and anti-inflammatory factor levels;The incidence of perioperative arrhythmias (atrial fibrillation, supraventricular tachycardia, ventricular premature beat >=6 times /min);Incidence of postoperative adverse reactions to esketamine;pain;Duration of stay in the recovery room;Discharge time;

Countries

China

Contacts

Public ContactZhou Hai

Xuzhou Central Hospital

zhouhai339339@163.com+86 189 5217 1368

Outcome results

None listed

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