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Effect of intraoperative infusion of different doses of esketamine on the quality of postoperative recovery in elderly patients undergoing knee arthroplasty

Effect of intraoperative infusion of different doses of esketamine on the quality of postoperative recovery in elderly patients undergoing knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099860
Enrollment
Unknown
Registered
2025-03-31
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

quality of postoperative recovery

Interventions

Group K1:Intraoperative intravenous pumping of esketamine 0.1mg/kg/h until 20min before the end of surgery
Group K2:Intraoperative intravenous pumping of esketamine 0.2mg/kg/h until 20min before the end of surgery
Group K3:Intraoperative intravenous pumping of esketamine 0.3mg/kg/h until 20min before the end of surgery
Group C:Intraoperative intravenous pumping of saline 10 ml/h until 20 min before the end of the operation

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. patients undergoing knee arthroplasty under elective general anesthesia; 2. age 65 years or older; 3. ASA classification I-III; 4. BMI 18-28 kg/m^2; 5. receiving postoperative patient-controlled intravenous analgesia (PCIA)

Exclusion criteria

Exclusion criteria: 1. allergy to any drug used in the study; 2. glaucoma, elevated intracranial pressure, hyperthyroidism, or pheochromocytoma; 3. uncontrolled or poorly controlled hypertension, class III hypertension (very high risk), severe cardiac arrhythmia, severe cardiovascular disease (atherosclerosis, coronary artery disease, cardiac insufficiency, pulmonary artery disease, pulmonary hypertension); 4. severe hepatic or renal insufficiency ( Child-Pugh class C or need for renal replacement therapy); 5. recent use of any tricyclic antidepressant, sedative, opioid, monoamine oxidase inhibitor, or sleep-inducing medication within the past month; 6. refusal to provide informed consent or inability to cooperate with investigators.

Design outcomes

Primary

MeasureTime frame
Postoperative quality of recovery scores;

Secondary

MeasureTime frame
Postoperative quality of recovery scores;NRS pain score;AIS Sleep Score;Time from surgery to extubation;PACU Length of Stay;Perioperative use of sufentanil, remifentanil, and propofol;Incidence of intraoperative hypotension, hypertension, tachycardia, bradycardia, and arrhythmia;Intraoperative use of vasoactive drugs;Incidence of postoperative adverse effects (nausea and vomiting, pain, hemodynamic instability, respiratory depression, agitation, etc.);Duration of surgery;First postoperative bed activity and length of hospital stay;The number of effective postoperative compressions and the amount of additional analgesic medication used;Hemodynamic indices at special moments in the perioperative period;

Countries

China

Contacts

Public ContactXiuxia Chen

Affiliated Hospital of Xuzhou Medical University

cxxlxy@sina.com+86 152 0520 0798

Outcome results

None listed

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