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Clinical study of preemptive analgesia with esmketamine in thoracoscopic lobectomy

Clinical study of preemptive analgesia with esmketamine in thoracoscopic lobectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039335
Enrollment
Unknown
Registered
2020-10-24
Start date
2020-10-20
Completion date
Unknown
Last updated
2021-01-25

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

Conditions

Lung cancer

Interventions

experimental group:Esketamine 0.5mg/kg was injected intravenously 5 minutes before 5min cutting
control group:Nil

Sponsors

Department of Anesthesiology, Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age 18-80 years old; ASA I-III Patients undergoing elective thoracoscopic lobectomy.

Exclusion criteria

Exclusion criteria: (1) Refusing to participate in this research; (2) Emergency operation; (3) Open operation; (4) Neurological, cognitive or mental diseases, including stroke, dementia, and schizophrenia with language disorders, or any disease that makes a meaningful postoperative visit impossible; (5) Cardiovascular disease: defined as low-output heart failure with preoperative left ventricular ejection fraction < 30%, active coronary artery disease, severe valvular heart disease with shortness of breath, symptomatic arrhythmia, pacemaker arrhythmia or AICD placement; (6) Complicated with severe lung, liver and kidney dysfunction.

Design outcomes

Primary

MeasureTime frame
NRS pain score at 2 hours, 6 hours, 12 hours, 24 hours and 48 hours after operation;

Secondary

MeasureTime frame
Incidence of PONV within 48 hours after operation;Ramsay sedation score;Dosage and number of postoperative analgesic remedies;Time of getting out of bed for the first time;The time of removing drainage tube after operation;Postoperative hospital stay;PCA pump press times;the first time after the operation to tolerate diet; Incidence of chronic pain after operation;

Countries

China

Contacts

Public ContactZhang Mengyuan

Shandong Provincial Hospital

zhangmy717@163.com+86 15168886767

Outcome results

None listed

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