Abortion surgery
Conditions
Interventions
Sponsors
The Affiliated Suzhou Science&Technology Town Hospital of Nanjing Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18-35 years; 2. American Anesthesiologists (ASA) Grade I-II; 3. Patients with elective painless abortion, single birth, 8-10 weeks of gestation; 4. Body mass index (BMI) 18-30kg/m^2; 5. Vital signs: respiratory rate >=10 and =95% when breathing air; systolic blood pressure (SBP) >=90mmHg and <=160mmHg; diastolic blood pressure (DBP); 6. Able to understand the research process and methods, and voluntarily participate in this research.
Exclusion criteria
Exclusion criteria: 1. Those who have general anesthesia contraindications or have a history of anesthesia accidents in the past; 2. Past history of vaginal delivery; 3. Abnormal uterine anatomy or other serious organic diseases; 4. Severe urinary ketone body 2+ or more in early pregnancy; 5. The patient has a history of artificial abortion within 3 months; 6. Known or suspected allergies or contraindications to propofol injection, cyclopofol injection excipients, benzodiazepines, opioids, muscle relaxants, etc.; 7. Patients with acute upper respiratory tract infection, asthma attack or acute severe throat disease; 8. Have a history of gastrointestinal diseases: gastrointestinal retention, active bleeding, possible reflux and aspiration, etc.; 9. Respiratory insufficiency, obstructive lung disease, difficult airway or difficult tracheal intubation (modified Markov score is III or IV); 10. Uncontrolled hypertension, hypotension and diabetes; 11. Severe arrhythmia, heart failure, unstable angina, myocardial infarction, etc.; 12. Severe liver dysfunction or severe renal insufficiency; 13. History of alcoholism or drug dependence; 14. Abuse or long-term use of narcotic, sedative, and analgesic drugs; 15. Those who have a history of mental illness; 16. Those who have participated in any drug clinical trial within 1 month before screening; 17. The investigator believes that there are any other subjects who are not suitable to participate in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anesthesia induction success rate; | — |
Countries
China
Contacts
Public ContactLi Hua
The Affiliated Suzhou Science&Technology Town Hospital of Nanjing Medical University
Outcome results
None listed