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Effect of lidocaine on postoperative analgesia and recovery quality of patients undergoing thoracoscopic surgery

Effect of lidocaine on postoperative analgesia and recovery quality of patients undergoing thoracoscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068840
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Thoracoscopic pneumonectomy

Interventions

Experimental group:PCIA: lidocaine 1.5mg/kg+flurbiprofen axetil 200mg+0.9% NS to 300ml
Control group:PCIA: sufentanil 2ug/kg+flurbiprofen axetil 200mg+0.9% NS To 300ml

Sponsors

Gansu Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-65 2.BMI 18-28 kg/m2 3.ASA classification I-? 4.Clear awareness, basic reading and understanding ability, basically normal vision and hearing, willing to participate in the study. 5.Being able to understand and sign the informed consent form, and cooperate in completing the intervention and evaluation

Exclusion criteria

Exclusion criteria: 1.People who are allergic to the drugs used in this study 2.Complicated with serious cardiovascular disease, liver or kidney dysfunction 3.Experience hyperalgesia or have a history of chronic postoperative pain 4.Have a history of drug or alcohol abuse 5.People with mental illness 6.Patients with peptic ulcer

Design outcomes

Primary

MeasureTime frame
Postoperative analgesia effect;

Countries

China

Contacts

Public ContactYan wenjun

Gansu Provincial People's Hospital

gsywj2008@hotmail.com+86 13893370700

Outcome results

None listed

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