General anesthesia
Conditions
Interventions
C1:Cyclopofol 0.4 mg/kg was injected intravenously
C2:Cyclopofol 0.5 mg/kg was injected intravenously
C3:Cyclopofol 0.6 mg/kg was injected intravenously
P:Propofol 2 mg/kg was injected intravenously
Sponsors
Sir Run Run Hospital Affiliated to Nanjing Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: 1. Patients receiving painless gastroscopy, regardless of gender, aged 18-64 years, BMI 18-30 kg/m2, ASA I or II; 2. Volunteer to participate in this research, and voluntarily sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Previously allergic to cyclopofol and propofol; 2. Combined with mental illness, abnormal liver and kidney function; 3. History of drug or alcohol abuse; 4. Severe cardiopulmonary disease; 5. Pregnancy or lactation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of successful sedation cases;The number of cases supplemented with cyclopofol or propofol;Wake up of time;Time of departure from hospital;Heart rate;Systolic blood pressure;Diastolic blood pressure;Pulse oxygen saturation;Pulse oxygen saturation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse reactions; | — |
Countries
China
Contacts
Public ContactWenbo Liang
Sir Run Run Hospital Affiliated to Nanjing Medical University
Outcome results
None listed