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Efficacy of the intraoperative opioid free anesthesia and analgesia on quality of patients' recovery and chronic pain in video-assisted thoracoscopic surgery

Efficacy of the intraoperative opioid free anesthesia and analgesia on quality of patients' recovery and chronic pain in video-assisted thoracoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069210
Enrollment
Unknown
Registered
2023-03-09
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Non-small cell lung cancer

Interventions

Group OFA:thoracic paravertebral block, esketamine, dexmedetomidine
Group OBA:opioid-based anesthesia and analgesia

Sponsors

Beijing Friendship Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients scheduled to undergo VATS partial pneumonectomy, aged >18 years and ASA grade ? - ?.

Exclusion criteria

Exclusion criteria: 1. Allergic or contraindicated to study drugs; 2. Chronic pain; 3. Severe liver dysfunction (total bilirubin >=2mg/dl); 4. Severe renal dysfunction (glomerular filtration rate 30kg m^2; 8. Dementia or obvious neurological diseases (such as stroke, epilepsy, intracranial tumors, Parkinson's disease history, etc.); 9. History of alcohol or drug abuse.

Design outcomes

Primary

MeasureTime frame
15-item recovery quality scale (QoR-15) 24 hours after surgery;

Secondary

MeasureTime frame
QoR-15 score 48 hours after surgery;3-minute diagnostic interview for CAM;Overall benefit of analgesic score satisfaction in pain treatment;Acute pain numeric rating scale score;Dosage of postoperative analgesics;Intensity of patient's chronic pain at rest;

Countries

China

Contacts

Public ContactWan Lei

Department of Anesthesiology, Beijing Friendship Hospital, Capital Medical University

wanleimz@sina.com+86 134 0106 7838

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026