painless induced abortion
Conditions
Interventions
Control group:propofol +normal saline
Experimental group:propofol +Flumazenil
Sponsors
First Hospital of Shanxi Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1. ASA grade I~II; aged 18 to 50 years; 2. Painless abortion surgery to relieve the curse; 3. Be informed about all the contents of this study and sign the consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with obvious respiratory, circulatory dysfunction, abnormal blood routine and blood biochemical indexes before surgery; 2. Patients with severe neuropsychiatric diseases; 3. Those suffering from infectious diseases; 4. Those who take benzodiazepines or opioids intermittently every day within 1 month or within the past 3 months; 5. Those who are allergic or contraindicated to benzodiazepines, opioids, propofol and other drugs and their components; 6. Patients who are judged to have difficulty in airway management: modified Markov score grade III and above; 7. Patients who are participating in other clinical trials; 8. The researchers believe that patients should not participate in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative quality recover scale; state of out of bed ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Eye opening time;Time to answer questions;Completion instruction time;Out of bed time; | — |
Countries
China
Contacts
Public ContactLi Tingyi
First Hospital of Shanxi Medical University
Outcome results
None listed