Postoperative nausea and vomiting
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age 18 or above (including 18) 2. ASA I~III level; 3. Body mass Index (BMI) : 18 to 35kg/m ² 4. Pregnant women who are scheduled to undergo electrocautery abortion under general anesthesia 5. Clearly understand and voluntarily participate in this research, and sign the informed consent form by oneself.
Exclusion criteria
Exclusion criteria: 1. History of chronic pain or acute pain before surgery, as well as long-term use of painkillers 2. There were symptoms of nausea and vomiting before the operation or antiemetic drugs were taken 3. Severe liver and kidney dysfunction 4. There was a history of depression or anxiety before the operation 5. Allergic to or contraindicated to the drug components involved in this study 6. Has participated in other drug clinical trials as a subject within the past three months 7. Patients who the researchers consider unsuitable to participate in this trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of postoperative nausea and vomiting;Intraoperative sedative and analgesic effects; | — |
Secondary
| Measure | Time frame |
|---|---|
| Surgeon satisfaction;Postoperative NRS score;The incidence of severe postoperative nausea and vomiting; | — |
Countries
China
Contacts
Tianjin Medical University General Hospital