nausea and vomit
Conditions
Interventions
experimental group:Tropisetron and propofol
Sponsors
People's Hospital of Three Gorges University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Gynecological surgery and postoperative intravenous analgesia; 2. Age: 18-64 years old; 3. ASA classification: I-II; 4. Body Mass index (BMI): 18-24 kg/m2; 5. Preoperative examination of heart, lung, liver and kidney function were normal; 6. Have the ability of independent behavior, clear consciousness and understand the investigation content; 7. Volunteers to participate in the study and sign the agreement.
Exclusion criteria
Exclusion criteria: 1. Patients with hypertension, heart disease, diabetes and other important systemic diseases with unsatisfactory control; 2. Long-term dependence on analgesics and other drugs; 3. History of allergy to propofol, toanisagar and other drugs; 4. A history of migraines; 5. Severe hyperlipidemia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| nausea rating;vomiting degree score;sedation scores;times of rescue; | — |
Secondary
| Measure | Time frame |
|---|---|
| satisfaction; based blood pressure;based heart rate;oxyhemoglobin saturation; | — |
Countries
China
Contacts
Public ContactZhaojun Qin
People's Hospital of Three Gorges University
Outcome results
None listed