None listed
Conditions
Interventions
Sponsors
Mindong Hospital Affiliated to Fujian Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: (1) Patients undergoing elective, painless induced abortion surgery (2) Age 18-45 years; (3)BMI18~28kg/m2 (4) Gestation time, 50-75 days; (5) Blood routine, coagulation routine, urine routine, white ribbon routine, liver and kidney function test results were unremarkable; (6) American Society of anesthesiologists (ASA) class I to II; (7) Informed of the experimental procedure and risks of anaesthesia, volunteered to participate in this study and signed consent for anaesthesia.
Exclusion criteria
Exclusion criteria: ?Patients with severe respiratory diseases; ?Patients with respiratory tract management difficulties:Modified Mallampati Score=III; ?HR<50 times/min,Atrioventricular block,Etc.Patients with severe arrhythmia; ?Patients with uncontrolled hypertension, hypotension and diabetes; ?Patients with severe liver and kidney dysfunction ?Patients with known or suspected allergy to propofol inj, benzodiazepines; ?Patients with alcoholism, drug abuse and chronic use of narcotic sedatives, narcotic analgesics, etc; ?Patients with mental illness ?Patients who have participated in clinical trials of any drug within 3 months; ?The investigator felt that there were any other conditions that were not suitable for participation in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative quality of recovery-15; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of nausea and vomiting after awakening;Injection pain;Time to discharge;Incidence of hypoxemia;Incidence of hypotension;The number and frequency of additional sedative drugs;Recovery time; | — |
Countries
China
Contacts
Public ContactDigui Weng
Mindong Hospital Affiliated to Fujian Medical University
Outcome results
None listed