Lung cancer with nausea and vomiting
Conditions
Interventions
Experimental group: Lidocaine group (Group A):Lidocaine was injected intravenously at 1.5mg/kg during anesthesia induction and pumped continuously at 2mg/kg/h during the operation until 5 minutes befo
Control group: Normal saline group (Group B):During anesthesia induction, saline with the same ml of lidocaine as the experimental group was injected intravenously, and saline with the same ML of lido
Sponsors
Chinese People's Liberation Army Western Theater Command General Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients undergoing elective thoracoscopic radical lung cancer surgery under general anesthesia were anesthetized 2. Female, ages 18-65 3. The method was intravenous general anesthesia 4.ASA grade I-III
Exclusion criteria
Exclusion criteria: 1. Patients with lidocaine allergy and contraindications 2. Previous thoracic surgery history 3. Use opioids, antiemetics, or corticosteroids within 24 hours before surgery 4. Preoperative radiotherapy and chemotherapy were performed 5. Serious cardiovascular and cerebrovascular diseases 6. Severe liver and kidney dysfunction 7. Complicated with mental illness 8. Uncooperative or unable to communicate with patients to complete postoperative follow-up
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nausea and vomiting;Pain score;Postoperative recovery quality; | — |
Countries
China
Contacts
Public ContactYang Haihong
Chinese People's Liberation Army Western Theater Command General Hospital
Outcome results
None listed