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Effect of perioperative application of esketamine on the quality of postoperative recovery in elderly patients undergoing laparoscopic abdominal surgery

Effect of perioperative application of esketamine on the quality of postoperative recovery in elderly patients undergoing laparoscopic abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102666
Enrollment
Unknown
Registered
2025-05-19
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Colorectal tumor

Interventions

Control group(C group):Administer an equal volume of normal saline at the same time during anesthesia induction and maintenance
Esketamine group (K group):The application of esketamine during the perioperative period

Sponsors

People's Hospital of Leshan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Elderly patients >=65 years of age, regardless of gender; 2.ASA physical condition class I-III; 3.Elective laparoscopic abdominal surgery with general anesthesia and intubation, expected to be extubated, and with a surgical duration of >=2 hours; 4.The subject or their family member signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Those who refuse to participate in the research and those who are unable to communicate due to aphasia, severe hearing impairment, or other difficulties; 2.Patients with diagnosed mental illnesses, such as schizophrenia, depression, and dementia; 3.Patients with a history of chronic pain or a history of substance abuse, including alcohol, opioids, or other psychotropic medications; 4.Those who have allergic reactions to any of the medications used in the study; 5.There is one contraindication for the use of esketamine injection: (1) High intraocular pressure (glaucoma) or penetrating ocular trauma; (2) Increased intracranial pressure; (3) Poorly controlled or untreated hypertension (systolic/diastolic blood pressure at rest: 180/100 mmHg); (4) Untreated or inadequately treated hyperthyroidism; 6.Critical illnesses: (1) Unstable angina pectoris or myocardial infarction occurred within 6 months. (2) Acute lung injury or acute respiratory distress syndrome within 3 months; respiratory failure, severe chronic obstructive pulmonary disease (GOLD grade III-IV). (3) Severe liver dysfunction (Child-Pugh grade C). (4) Glomerular filtration rate < 30 ml/min. (5) Heart failure (NYHA cardiac function grade III-IV); 7.Those who have already participated in clinical studies of other drugs or medical devices;

Design outcomes

Primary

MeasureTime frame
Quality of recovery scores (QoR-15);

Secondary

MeasureTime frame
Quality of recovery scores (QoR-15);Opioid consumption;The time for intestinal function recovery(The time from tracheal extubation to the first passage of flatus);Adverse reactions (moderate to severe nausea and vomiting, restlessness, delirium, hallucination, nightmare, diplopia, dizziness);The 30-day all - cause mortality rate after surgery;The number of postoperative hospital stay days (the number of days from the day of surgery to the day of discharge);Score of the Hospital Anxiety and Depression Scale;Numeric rating scales;Sleep quality;

Countries

China

Contacts

Public ContactSong Lai

People's Hospital of Leshan

18284306100@163.cm+86 18284306100

Outcome results

None listed

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