Painless induced abortion
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. The subjects with accurate and complete clinical data; 2. Aged 18 to 46 years, ASA grade I-II, BMI 18-28 kg / m2; 3. No patients with liver and kidney dysfunction, shock and cardiopulmonary dysfunction; 4. Those who have the ability of reading and understanding; have the knowledge of this research and participate voluntarily.
Exclusion criteria
Exclusion criteria: 1. Patients with obvious respiratory and circulatory dysfunction, abnormal blood routine and blood biochemical indexes before operation; 2. Patients with severe neuropsychiatric diseases; 3. Patients with infectious diseases; 4. Patients who took benzodiazepines or opioids every day or in recent 3 months within 1 month; 5. Patients who are allergic or contraindicated to benzodiazepines, opioids, propofol, flumazenil, naloxone and other drugs; 6. Patients with respiratory tract management difficulties: modified Markovian score grade III and above.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HR, RR, SPO2, NBP and BIS of the subjects after starting administration until the end of operation were stable, and the continuous change trend (diachronic change) was recorded.;MOAA/S score during operation;The time from the end of the last dose until the subject is fully awake;The standard time for subjects to leave the hospital after the operation;Incidence of injection pain; | — |
Countries
China
Contacts
Jingzhou First People's Hospital