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Effect of esketamine on postoperative pain in Patients Undergoing Lumbar Vertebral Surgery

Effect of esketamine on postoperative pain in Patients Undergoing Lumbar Vertebral Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071835
Enrollment
Unknown
Registered
2023-05-26
Start date
2023-05-29
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

postoperative pain

Interventions

Control group:Same volume of physiological saline
Low-dose of esketamine group:Low-dose of esketamine

Sponsors

Xuzhou Central Hospital, Jiangsu Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age: 18~65 years old; American Society of Anesthesiologists (ASA) Grade - Class; BMI18.5 ~ 29.9 kgm2

Exclusion criteria

Exclusion criteria: History of esketamine allergy; History of alcohol or analgesic drug dependence; History of severe hypertension and severe heart, liver, lung, and kidney dysfunction; History of serious infectious diseases, immune system disorders, and hematologic disorders; History of cognitive dysfunction; History of depression, psychiatric illness; 7. patients with serious infectious diseases, immune system diseases and blood system diseases

Design outcomes

Primary

MeasureTime frame
Time of first pressure on the analgesia pump;—

Secondary

MeasureTime frame
Amount of anesthetic drugs;Postoperative adverse reaction;Postoperative pain score;—

Countries

China

Contacts

Public ContactBin Sun

Xuzhou Central Hospital, Jiangsu Province

sun_bin66@163.com+86 158 5215 2417

Outcome results

None listed

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