Postoperative Nausea and Vomiting
Conditions
Interventions
Control group:No intervention
Sponsors
China Medical University Affiliated Shengjing Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1: Under general anesthesia, perform a total hysterectomy 2: Age 18-60 years old 3: ASA Classification I-II 4: Apfel score is greater than or equal to 2 points 5: Able to understand, sign the informed consent form, and coordinate interventions and assessments
Exclusion criteria
Exclusion criteria: 1: Pregnant and lactating patients 2: Contraindications such as skin allergies or rupture, test point infection or itching, adhesive tape allergies, implanted pacemakers, etc 3: Severe cardiovascular diseases (myocardial infarction, heart failure, malignant arrhythmias, etc.) 4: Having a history of alcohol, opioid, or other drug abuse 5: May require ICU stay after surgery 6: Participated in other clinical studies within 3 months before enrollment in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of postoperative nausea and vomiting; | — |
Secondary
| Measure | Time frame |
|---|---|
| Number ofvomiting episodes;First flatus time after surgery;Postoperative pain score;Ultrasound observation comparing the size of the stomach before and after surgery; | — |
Countries
China
Contacts
Public ContactHan Guang
China Medical University Affiliated Shengjing Hospital
Outcome results
None listed