Skip to content

The Impact of Different Doses of Esketamine Infusion on the Quality of Early Postoperative Recovery in Elderly Patients Undergoing Thoracoscopic Pulmonary Surgery

The Impact of Different Doses of Esketamine Infusion on the Quality of Early Postoperative Recovery in Elderly Patients Undergoing Thoracoscopic Pulmonary Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101838
Enrollment
Unknown
Registered
2025-04-30
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Pulmonary disease

Interventions

Control Group (Group C):Routine intravenous anesthetic maintenance during surgery, without esketamine. Normal saline was continuously infused at an equivalent rate until skin closure.
Low-Dose Esketamine Group (Group ES1):In addition to the maintenance of conventional intravenous anesthetics, esketamine 0.125 mg·kg^-1·min^-1 was continuously infused intravenously to the suture.
Medium-Dose Esketamine Group (Group ES2):In addition to the maintenance of conventional intravenous anesthetics, esketamine 0.250 mg·kg^-1·min^-1 was continuously infused intravenously to the suture.

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1.Both male and female patients are eligible. 2.Age range: 65 to 79 years. 3.Body mass index (BMI): 18 kg/m^2 < BMI < 30 kg/m^2. 4.American Society of Anesthesiologists (ASA) physical status classification: I to III. 5.Elderly patients scheduled to undergo thoracoscopic lobectomy or segmentectomy for lung cancer.

Exclusion criteria

Exclusion criteria: 1.History of cardiovascular diseases, including hypertension, coronary heart disease, and arrhythmia. 2.Preoperative endocrine disorders or severe hepatic/renal dysfunction. 3.History of stroke within the past 3 months. 4.Allergy or contraindication to propofol, opioids, ketamine, or their components. 5.History of psychiatric disorders. 6.Participation in any drug clinical trial within the last 3 months. 7.Those who are allergic to or contraindicated to propofol, opioids, ketamine and other drugs and their drug components.

Design outcomes

Primary

MeasureTime frame
QoR-15 scores;

Secondary

MeasureTime frame
The Intraoperative Esketamine Dose;Visual Analog Scale (VAS) scores during activity (coughing) at 6 hours after surgery ;The incidence of dizziness within 48 hours after surgery;Time from the end of surgery to tracheal extubation;post-anesthesia care unit (PACU) stay duration;Cumulative postoperative oxycodone dose at 48h;The incidence of postoperative nausea and vomiting (PONV) within 48 hours after surgery, ;The incidence of delirium within 48 hours after surgery;The incidence of hallucinations within 48 hours after surgery;The incidence of nightmares within 48 hours after surgery;The incidence of somnolence within 48 hours after surgery;The incidence of constipation within 48 hours after surgery;Patient satisfaction after surgery;Visual Analog Scale (VAS) scores during activity (coughing) at 12 hours postoperatively;Visual Analog Scale (VAS) scores during activity (coughing) at 24 hours postoperatively;Visual Analog Scale (VAS) scores during activity (coughing) at 48 hours postoperatively;Cumulative postoperative oxycodone dose at 24h;The Intraoperative Remifentanil Dose;The Intraoperative Sufentanil Dose;Total number of PCA pump presses s at postoperative 24h ;Number of effective PCA pump presses at postoperative 24h ;Total number of PCA pump presses s at postoperative 48h ;Number of effective PCA pump presses at postoperative 48h;

Countries

China

Contacts

Public ContactMa Yanhui

Xuanwu Hospital, Capital Medical University

peep2005@163.com+86 158 1093 0059

Outcome results

None listed

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