Painless induced abortion
Conditions
Interventions
Propofol group:Intravenous injection of Propofol 1.6mg/kg
Sponsors
The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18-45 years; 2. American Anesthesitist Grade (ASA) grade I-II; 3. Body mass index (BMI) 18-30kg/m^2; 4. Vital signs: respiratory frequency >= 10 and = 95%; systolic blood pressure (SBP) >= 90 mmHg and = 60 mmHg and = 55 and <= 100 times/min; 5. Understand the study process and methods, and voluntarily participate in this study.
Exclusion criteria
Exclusion criteria: 1. Associated with a contraindication to venous general anesthesia or has a previous history of unexpected anesthesia; 2. Known or suspected to be allergic or contraindication to propofol injections, cipofol injection excipients; 3. Combined with cerebral brain loss, intracranial hypertension, stroke, unstable angina pectoris, and myocardial infarction; 4. Respiratory insufficiency, obstructive pulmonary disease, presence of difficult airway or judged tracheal intubation difficulty (modified Marsh score grade III or IV); 5. Uncontrolled diabetes mellitus or hypertension; 6. Has severe liver dysfunction or severe renal insufficiency; 7. History of alcoholism or drug dependence; 8. Abuse or long-term application of anesthesia, sedation, and analgesic drugs; 9. With a previous history of mental illness; 10. Those who had participated in any drug clinical trial within 1 month prior to the screening; 11. The investigator considered any other subjects unsuitable to participate in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Success rate of anesthesia induction; | — |
Countries
China
Contacts
Public ContactQi Qingling
The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Outcome results
None listed