Pain after uvula palatopharyngeal reconstruction surgery
Conditions
Interventions
Experimental group:Before induction of general anesthesia, intravenous injection of lidocaine 1.5mg/kg/10 min was administered according to the patient's standard body weight, followed by intravenous
Control group:Before induction of general anesthesia, intravenous injection of physiological saline at a dose of 1.5mg/kg/10min according to the patient's standard body weight was administered, follow
Sponsors
Shenzhen Longgang DIstrict ENT Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1.Patients planning to undergo elective UPPP 2. Age range of 18-60 years old
Exclusion criteria
Exclusion criteria: 1.Refusal to sign informed consent form 2. Allergy to lidocaine 3. Liver dysfunction 4. Severe heart disease or heart dysfunction 5. Pregnant women 6. Central nervous system disorders 7. History of alcohol/drug abuse 8. Chronic pain patients who regularly use opioid drugs or have abnormal pain perception
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score;Postoperative Recovery Quality Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total amount of opioid use during and after surgery;Postoperative minimum oxygen saturation;Incidence of blood oxygen saturation below 90%;Incidence of adverse reactions related to opioid drugs;Incidence of adverse reactions related to local anesthetics;Total length of hospitalization; | — |
Countries
China
Contacts
Public ContactHongji Zhou
Shenzhen Longgang DIstrict ENT Hospital
Outcome results
None listed