Randomized controlled clinical trial of the efficacy and safety of cyclopofol for general anesthesia induction in elderly and preelderly women
Conditions
Interventions
Cyclophenol group :Cyclopolol group anesthesia induction was 0.4mg/kg
propofol group:Propofol group anesthesia induction was 2mg/kg
Sponsors
International Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University
Eligibility
Sex/Gender
Female
Age
45 Years to 75 Years
Inclusion criteria
Inclusion criteria: Female (75=aged>45) Body Mass index (BMI) =18;<30 kg/m2; Elective gynecological operations; ASAI~II; Be able to understand the research process and methodology and participate in the study voluntarily.
Exclusion criteria
Exclusion criteria: Patients with severe organ dysfunction such as heart, lung, liver and kidney; Those who have contraindicated evidence of the drugs used in this study; Long-term users of opioids; Participants in other clinical trials within 3 months before the trial; Who the researchers thought should not be included.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hemodynamic index;successful induction rate of general anesthesia ;Minimum systolic blood pressure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Occurrence of adverse events during the trial ;time to successful induction of general anesthesia ;bispectral index value ; | — |
Countries
China
Contacts
Public ContactZifeng Xu
The International Peace Maternity and Child Health Hospital-Shanghai JiaoTong University School of Medicine
Outcome results
None listed