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Does the systemic lidocaine improve the quality of recovery after video-assisted thoracic surgery?

Efficacy of systemic lidocaine on postoperative quality of recovery after video-assisted thoracic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027515
Enrollment
Unknown
Registered
2019-11-17
Start date
2019-11-21
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

lung cancer

Interventions

Experimental group:A single infection of lidocaine 1.5mg/kg and then a continuous infusion of 2mg/kg/h until the surgery is over
placebo group:equal volumes of saline

Sponsors

Anesthesia department of Fujian Provincal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. ASA status I or II; 2. Aged over 18 years; 3. video-assisted thoracic surgery.

Exclusion criteria

Exclusion criteria: 1. severe arrhythmia; 2. having a history of chronic opioids; 3. severe hepatic and renal dysfunction; 4. epilepsy and other disease that may affect this study.

Design outcomes

Primary

MeasureTime frame
quality of recovery;—

Secondary

MeasureTime frame
Postoperative acute pain intensity;Postoperative cumulative 48h opioids consumption;the time to recovery of bowel function;the incidence of PONV;the patient‘s satisfaction;awaking time of anesthesia;—

Countries

China

Contacts

Public ContactYusheng Yao

Fujian Provincal Hospital

fjslyys@126.com+86 13559939629

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026