painless induced abortion
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Accurate and complete clinical data;(2) age 18 to 46, ASA class ? ~ ?, BMI 18 ~ 28 kg/m2;(3) No dysfunction of important organs such as liver and kidney, shock and cardiopulmonary dysfunction;(4) Ability to read and understand;Informed and voluntary participation in this study.
Exclusion criteria
Exclusion criteria: (1) Patients with obvious respiratory and circulatory dysfunction, abnormal blood routine and blood biochemical indicators before operation;(2) persons suffering from severe neuropsychiatric diseases;(3) persons suffering from infectious diseases;(4) Taking benzodiazepines or opioids every day for one month or for nearly three months intermittently;(5) Allergic or contraindicated to benzodiazepines, opioids, propofol, flumazine, naloxone and other drugs and their components;(6) judged: patients with difficult airway management improved markov score ? level 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