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Effect of continuous intraoperative infusion of esketamine on the subjective quality of postoperative recovery in nonstop cardiac coronary artery transplantation

Effect of continuous intraoperative infusion of esketamine on the subjective quality of postoperative recovery in nonstop cardiac coronary artery transplantation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091362
Enrollment
Unknown
Registered
2024-10-28
Start date
2024-10-28
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

coronary heart disease

Interventions

Esketamine group:0.2mg/kg/h esketamine pumped via cvp after central venous placement
control group:50 ml syringe pumped into saline, pumped 0.2 mg/kg/h

Sponsors

Central Hospital of Dalian University of Technology (Dalian Municipal Central Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients aged =18 years , with a BMI of 18.5 to 23.9 kg/m^2, and those aged 65 years or older with a BMI of 20 to 26.9 kg/m^2 who underwent nonstop cardiac coronary artery transplantation.

Exclusion criteria

Exclusion criteria: a. Patients with hepatic or renal failure. b. Ketamine Ketamine allergy. c. Psychiatric illness or history of psychiatric drug use. History of drug abuse. d. Patients with uncontrolled hypertension, increased intracranial pressure, high intraocular pressure, and patients with hyperthyroidism. e. Patients taking medications that affect immune function. f. History of cardiac major vascular surgery. g. Preoperative radiotherapy and chemotherapy. h. Patients who are unable to complete the scale assessment.

Design outcomes

Primary

MeasureTime frame
QoR-15;

Secondary

MeasureTime frame
Intraoperative circulatory stability;NRS scores 1, 2, and 3 days after awake extubation;Anxiety, depression scores;postoperative adverse reaction;Extubation and hospitalization time;Postoperative review of CTA results;30-day postoperative mortality rate;

Countries

China

Contacts

Public ContactYi Chang

Central Hospital of Dalian University of Technology (Dalian Municipal Central Hospital)

jordon1986@163.com+86 159 9862 8366

Outcome results

None listed

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