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Effect of low-dose esketamine on intraoperative hypoxemia in patients undergoing thoracoscopic nontracheal intubation anesthesia: a double-blind, randomized controlled study

Effect of low-dose esmketamine on intraoperative hypoxemia in patients undergoing thoracoscopic surgery under non-tracheal intubation anesthesia: a double-blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094821
Enrollment
Unknown
Registered
2024-12-27
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Intraoperative complications of thoracoscopy

Interventions

Esketamine Group (E):The patient was administered 0.2 mg/kg of esketamine during the induction of anesthesia.
Saline placebo group (Group A):The same dose of normal saline was administered during anesthesia induction.

Sponsors

Shandong Provincial Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-65 years old; (2) ASA Grade I ~II; (3) BMI 18-28 kg/m^2; (4) Patients undergoing non-tracheal intubation anesthesia thoracoscopic surgery; (5) Patients who sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients who are allergic to esketamine or have drug contraindications; (2) Secondary surgery or resection of tracheal tumor; (3) A history of neurological disease or mental illness; (4) Preoperative pulmonary function examination FEV1<60% or respiratory system infection.

Design outcomes

Primary

MeasureTime frame
The incidence of hypoxemia and the time to its onset, with hypoxemia defined as an intraoperative SpO2 <=90% lasting for at least 10 s.;

Secondary

MeasureTime frame
Incidence of intraoperative hypercapnia (PCO2 >= 60 mmHg);Concentrations of IL-6 and IL-8 at the end of surgery;Postoperative visual analogue scale score;Time to recovery of spontaneous respiration after laryngeal mask placement;Time to laryngeal mask removal (measured from the end of surgery);The awakening time;Incidence of bradycardia (heart rate [HR] 20% reduction in blood pressure from the baseline value);Incidence of = 24 h postoperative nausea and vomiting and hoarseness;Time to ambulation, drinking, and eating postoperatively;Incidence of pulmonary complications within 2 weeks postoperatively;Length of hospital stay;

Countries

China

Contacts

Public ContactGu Changping

Shandong Provincial Hospital Affiliated to Shandong First Medical University

jsmggcp@163.com+86 158 0660 7957

Outcome results

None listed

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