Application of Lidocaine in Clinical Anesthesia
Conditions
Interventions
Control group:Anesthesia with propofol alone
Experimental group:Anesthesia with propofol combined with lidocaine
Sponsors
Fujian Provincial Maternity and Children's Hospital
Eligibility
Sex/Gender
All
Age
1 Years to 12 Years
Inclusion criteria
Inclusion criteria: 1. Subjects of ASA I-II; 2. Full term children.
Exclusion criteria
Exclusion criteria: 1. Newborns or subjects over 18 years old; 2. Subjects with renal failure; 3. Subjects with liver dysfunction; 4. Subjects with history of epilepsy; 5. Patients with severe arrhythmia; 6. Subjects allergic to lidocaine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Propofol usage; | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of episodes of low oxygen saturation;Anesthesia recovery time;VAS pain score;Blood pressure;heart rate; | — |
Countries
China
Contacts
Public ContactLongxin Zhang
Fujian Maternal and Child Health Care Hospital
Outcome results
None listed