Burn
Conditions
Interventions
Control group, experimental group:Anesthesia induction and postoperative analgesia using Sufentanil
Experimental group:Anesthesia induction and postoperative analgesia using oxaliplatin
Sponsors
Heze Municipal Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.ASAI and II grade patients, aged 18-75 years, 2. BMI 18-28 kg/m2, 3.with mild to moderate burns.
Exclusion criteria
Exclusion criteria: 1.History of cardiovascular and pulmonary dysfunction, with pulmonary function indicating moderate to severe pulmonary ventilation dysfunction; Patients with heart failure and circulatory failure, etc. For patients allergic to oxaliplatin and sufentanil; 2.Participated in other clinical trials within 4 weeks prior to the start of the study; Emergency patients who cannot undergo sufficient preoperative preparation; Patients with organic heart disease before surgery (such as sinus syndrome, atrioventricular block, etc.); 3.Patients with severe dehydration, electrolyte imbalance, and shock; Pregnant, planned pregnant, or lactating female patients; Patients with neurological or psychiatric disorders, severe alcohol abuse, and a history of long-term high-dose use of sedatives; 4.Patients with severe respiratory dysfunction before surgery; Acute or severe bronchial asthma in an unmonitored environment or without resuscitation equipment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numerical Simulation Score (NRS); | — |
Secondary
| Measure | Time frame |
|---|---|
| Wake-up time; | — |
Countries
China
Contacts
Public ContactGuo jiyan
Heze Municipal Hospital
Outcome results
None listed