painless hysteroscopy
Conditions
Interventions
Low dose group (group L):Oliceridine fumarate 0.5mg+ propofol
Medium dose group (M group):Oliceridine fumarate 1mg+ propofol
Sponsors
The Afffliated Shunde Hospital of Jinan University, Foshan, China
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Age 18-60 years old, BMI 18-28 kg /m^2, Mallampati grade ? or ?, no airway, head and neck conditions; 2. ASA grade I or II; 3. patients scheduled for elective hysteroscopy; 4. Patients volunteered to participate in the study.
Exclusion criteria
Exclusion criteria: 1. Patients who refuse to participate or who are not suitable for the trial; 2. allergic to propofol or oliceridine fumarate; 3. severe cardiovascular, pulmonary, liver and kidney dysfunction or adrenal cortex dysfunction; 4. Use of alcohol, psychotropic drugs or analgesics within 24 hours before surgery; 5. epileptic seizures; 6. a history of psychological problems or mental illness; 7. history of hyperthyroidism; 8. airway hyperresponsiveness disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body movement;frown;Ramsay score <5; | — |
Secondary
| Measure | Time frame |
|---|---|
| blood pressure;SPO2; | — |
Countries
China
Contacts
Public ContactChen Jinming
The Afffliated Shunde Hospital of Jinan University, Foshan, China,
Outcome results
None listed