not limited
Conditions
Interventions
1:propofol 1mg/kg was given by intravenous
2:propofol 2mg/kg was given by intravenous
Sponsors
Department of Anesthesiology, West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: 1. patients with ASA 1-2grade; 2. patients aged 18-55 years old; 3. patients with elective surgical procedures and endotracheal intubation of general anesthesia; 4. Paients participating in the test voluntarily and signing informed consent signed.
Exclusion criteria
Exclusion criteria: 1. body mass index >30kg/m2; 2. patients with expected difficult airway; 3. patients with electrolyte and acid-base disorders especially hyperkalaemia or significant hyperkalae-mia risk; 4. patients with neuromuscular disease or taking drugs influencing nerve muscle function; 5. patients using sedation and analgesia drug before surgery; 6. patients with history of allergic reaction to propofol;patient with mental illness and epile- psy;patients with family history of Malignant hyperthermia; 7. patients with serious diseas in liverkidneycardiovascular and respiratory system.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| tracheal intubating condition; | — |
Countries
China
Contacts
Public ContactWang Jian
Outcome results
None listed