Infertility
Conditions
Interventions
O1C1:Oxycodone 0.05 mg/kg
Ciprofol 0.3 mg/kg
O1C2:Oxycodone 0.05 mg/kg
Ciprofol 0.35 mg/kg
O1C3:Oxycodone 0.05 mg/kg
Ciprofol 0.4 mg/kg
O1C4:Oxycodone 0.05 mg/kg
Ciprofol 0.45 mg/kg
O1C5:Oxycodone 0.05 mg/kg
Ciprofol 0.5 mg/kg
O2C1:Oxycodone 0.075 mg/kg
O2C2:Oxycodone 0.075 mg/kg
O2C3:Oxycodone 0.075 mg/kg
O2C4:Oxycodone 0.075 mg/kg
O2C5:Oxycodone 0.075 mg/kg
Sponsors
The First Affiliated Hospital of Hebei North University
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Female patients of childbearing age undergoing elective ultrasound-guided painless oocyte retrieval; 2. Aged 20–45 years; 3. With body mass index (BMI) of 18.5–28.0 kg/m^2; 4. And ASA physical status ? or ?.
Exclusion criteria
Exclusion criteria: 1. Severe systemic diseases, including but not limited to severe respiratory or cardiovascular disorders; 2. Clearly difficult airway; 3. Known allergy or contraindication to the study drugs oxycodone and ciprofol, or to any of their components; 4. History of asthma; 5. History of long-term analgesic use; 6. Allergy to any of the medications used; 7. Confirmed difficult airway; 8. High ovarian position requiring external abdominal pressure assistance; 9. Surgical duration = 30 minutes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Heart rate;Systolic blood pressure;Diastolic blood pressure;Mean arterial pressure;Additional dose of Ciprofol;Wake-up time;Incidence of Adverse Reactions;Lower abdominal pain score at 1 hour postoperatively; | — |
Countries
China
Contacts
Public ContactYan Xiaowen
The First Affiliated Hospital of Hebei North University
Outcome results
None listed