Anesthesiology
Conditions
Interventions
ciprofol: ciprofol
Sponsors
The Fourth Affiliated Hospital, Zhejiang University School of Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1)Day surgery, intubation under general anesthesia 2)18 years old < age < 60 years old 3) ASA I-II level 4)18 kg/m2<BMI<28 kg/m2 5)Voluntarily participate in this study and sign informed consent
Exclusion criteria
Exclusion criteria: Change of surgical mode; Having a severe allergic reaction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sedative effect (sedative induction time, operative time, sedative waking time, etc); | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of adverse reactions such as injection pain,hypotension,respiratory depression and hypoxemia;Patient satisfaction and surgeon satisfaction; | — |
Countries
China
Contacts
Public ContactJianhong-Xu
Outcome results
None listed