None listed
Conditions
Interventions
Group P:Propofol 20 mg
Group C:Cyclophenol 2.5 mg
Group S:Sodium Chloride Physiological Solution 2ml
Sponsors
Weifang People's Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Gynecological patients who are scheduled to undergo hysteroscopy under total intravenous anesthesia; 2. ASA I-II grade; 3. BMI 18-28; 4. Aged 18-65 years.
Exclusion criteria
Exclusion criteria: 1. Patients who are allergic to any ingredients such as benzodiazepine opioids propofol and micuramide; 2. Patients with schizophrenia and severe depression; 3. Acute upper respiratory tract infection; 4. Poorly controlled severe hypertension; 5. History of alcohol abuse and long-term use of sedative analgesics and history of allergies; 6. Markov airway classification grade IV, those who require awake tracheal intubation as determined by the investigator; 7. Breastfeeding period female; 8. Other circumstances determined by the researcher to be unsuitable for selection; 9. The operation time is more than 1 hour; 10. Patients who have been hospitalized for more than 24 hours; 11. Patients who have been dropped out after surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of nausea and vomiting; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time the patient fell asleep;Changes in hemodynamics at different times;Time of anesthesia;Remazolam dose; | — |
Countries
China
Contacts
Public ContactJi Fanceng
Weifang People's Hospital
Outcome results
None listed