anesthesia
Conditions
Interventions
control group:propofol
treatment group :ciprofol
Sponsors
Chengdu Jinjiang Maternal and child Health Care Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Aged 18 to 35 years; 2. BMI>=18 kg/m2 and =95%, SBP>=90mmHg; DBP>=60mmHg; 5. Sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Those with contraindications to general anesthesia or a history of anesthesia accident in the past; 2. Kidney or liver disease; 3. Any heart disease and respiratory system disease; 4. History of hypertension; 5. Abuse of alcohol or other drugs within 3 months; 6. There may be difficult airway; 7. Prepare for pregnancy within one month; 8. Respiratory tract infection within one week; 9. Subjects who are considered by the investigator to have any other factors that are not suitable for participating in this clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of respiratory related adverse events; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hysteroscopy examination diagnosis and treatment completion rate;Incidences of circulation-related adverse events;Incidence of postoperative dizziness;Incidence of postoperative nausea and vomiting;Incidence of intraoperative body movement;Injection pain score;Vital signs;Drug top-up times;Postoperative satisfaction scores of patients and anesthesiologists; | — |
Countries
China
Contacts
Public ContactJia Fei
Chengdu Jinjiang Maternal and child Health Care Hospital
Outcome results
None listed