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Effects of different doses of esmketamine on remifentanil-induced hyperalgesia in patients undergoing thoracoscopic surgery at different times

Effects of different doses of esmketamine on remifentanil-induced hyperalgesia in patients undergoing thoracoscopic surgery at different times

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083093
Enrollment
Unknown
Registered
2024-04-15
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

hyperalgesia

Interventions

Morning Control Group:Normal saline infused at induction, maintained until the end of surgery
Afternoon Control Group:Normal saline infused at induction, maintained until the end of surgery
Morning Dose 1:Esketamine infusion 0.2 mg /kg at induction, 2µg/kg/min maintained until the end of surgery
Afternoon Dose 1:Esketamine infusion 0.2 mg /kg at induction, 2µg/kg/min maintained until the end of surgery
Morning Dose 2:Esketamine infusion 0.4mg /kg at induction, 4µg/kg/min maintained until the end of surgery
Afternoon Dose 2:Esketamine infusion 0.4 mg /kg at induction, 4µg/kg/min maintained until the end of surgery

Sponsors

The Third Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: ASA : II-III 2: Thoracoscopic surgery was planned and the duration of surgery was estimated to be 1 to 3 hours 3: Normal thinking and intelligence development, able to understand and sign informed consent, able to cooperate with the experiment 4: The right hand is dominant 5: patients who voluntarily underwent PCIA

Exclusion criteria

Exclusion criteria: 1: accompanied with serious cardiovascular, liver, kidney and other organ system diseases 2: pregnant or lactating women 3: acute and chronic pain such as chronic headache, low back pain and neuropathic pain 4: recent or long-term use of anti-inflammatory drugs, opioids or related disease treatment drugs 5: heavy smoking or drinking 6: patients with frailty or obesity 7: patients allergic to opioids, esketamine, and non-steroidal drugs 8: untreated or poorly controlled hypertension 9: glaucoma, intracranial hypertension and hyperthyroidism 10: patients with neurological and psychiatric disorders

Design outcomes

Primary

MeasureTime frame
postoperation 24h AUC of Moving Pain NRS;

Secondary

MeasureTime frame
Pressure pain threshold;Consumption of analgesics;

Countries

China

Contacts

Public ContactHuiting Liu

The Third Affiliated Hospital of Chongqing Medical University

650539@hospital.cqmu.edu.cn+86 199 2325 6802

Outcome results

None listed

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