None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients undergoing video-assisted thoracoscopic (VATS) lobectomy 2) Patients aged 19 years or older and younger than 84 years 3) Patients classified as American Society of Anesthesiologists (ASA) Physical Status I, II, or III 4) Patients who provided written informed consent prior to participation in the study
Exclusion criteria
Exclusion criteria: 1) Patients with a history of adverse reactions to local anesthetics 2) Patients with abnormal coagulation profiles (e.g., INR > 1.5) 3) Pregnant or breastfeeding patients 4) Patients with morbid obesity (body mass index [BMI] > 30 kg/m²)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of recovery score (Quality of Recovery-15K Survey ) | — |
Secondary
| Measure | Time frame |
|---|---|
| NRS(Numeric rating scale) pain score;Total opioid consumption over 24 hours (measured in morphine milligram equivalents, MME);Additional opioid consumption administered in the post-anesthesia care unit (PACU);Time to first analgesic administration after PACU discharge (defined as NRS > 5);Incidence of postoperative nausea and vomiting (PONV) | — |
Countries
Korea, Republic of
Contacts
Kangbuk Samsung Medical Center