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Perioperative effects of lidocaine intravenous infusion in patients undergoing video-assisted thoracic pulmonary resection surgery

Perioperative effects of lidocaine intravenous infusion in patients undergoing video-assisted thoracic pulmonary resection surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095861
Enrollment
Unknown
Registered
2025-01-14
Start date
2023-12-04
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Thoracic diseases requiring thoracoscopic surgery

Interventions

Experimental group (Group L):Slow intravenous injection of 1.5 mg/kg of lidocaine over 10 min before induction and continuous pumping of lidocaine at a rate of 2.0 mg/kg/h after intubation until the e
Control group (Group N):The same volume of saline was given as placebo.

Sponsors

Tongling People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients with ASA classification I-III, age >= 18 years, and proposed elective transvideo-assisted thoracoscopic surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: (1) Severe hepatic, renal and endocrine abnormalities; (2) Neuropsychiatric disorders, neuromuscular disorders; (3) Allergy to amide local anesthetics; (4) Severe cardiac disease (severe arrhythmia, Adame-Strokes syndrome, III degree AV block, preexcitation syndrome, congestive heart failure, etc.) prior to the operation; (5) Electrolyte disorders, epileptic seizures, pregnancy or breastfeeding; (6) chronic lung diseases (pulmonary cystic fibrosis, bronchial dysplasia, pulmonary hypertension, chronic obstructive pulmonary disease, etc.) or abnormal pulmonary function tests; (7) BMI >= 30 kg/m^2; (8) preoperative inspiratory pulse oximetry of less than 95% due to neocoronary pneumonitis, etc.; and (9) refusal to participate in the trial or to sign the test by the patients themselves or their families.

Design outcomes

Primary

MeasureTime frame
Quality of Recovery (QoR-40) score at 24h postoperatively;

Secondary

MeasureTime frame
Incidence of PPCs within 7 days of surgery;Hemodynamic changes in patients after induction and intubation;VAS PAIN SCORE;

Countries

China

Contacts

Public ContactZhu Mudan

Tongling People's Hospital

19905625176@163.com+86 199 0562 5176

Outcome results

None listed

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