None
Conditions
Interventions
Experimental group:Before the examination, sufentanil 0.1 µg/kg was administered intravenously (for standardized analgesia). The induction dose: in the propofol group, it was 20 mg/kg administered int
Control group:Before the examination, sufentanil 0.1 µg/kg was administered intravenously for preoperative analgesia. The induction dose: propofol 2.0 mg/kg was injected intravenously.
Sponsors
Jintang County First People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Age: 18 - 70 years old; ASA classification: I - III; Cardiac function: 1 - 3; Scheduled for elective painless gastroscopy; 2. Sign the informed consent form
Exclusion criteria
Exclusion criteria: 1. Allergic to propofol or soybeans/eggs; 2. Severe liver or kidney dysfunction (Child-Pugh C grade, eGFR < 30 mL/min); 3. Pregnant or lactating women; 4. Complicated with severe central nervous system diseases (such as uncontrolled epilepsy);
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anesthesia success rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Success rate of sedation;The incidence of injection pain;The number of additional administrations of propofol and propofol phosphate;Anesthesia recovery quality: Time to full consciousness, Time to discharge from hospital; | — |
Countries
China
Contacts
Public ContactQu Yang
Jintang County First People's Hospital
Outcome results
None listed