postoperative nausea and vomiting
Conditions
Interventions
Sponsors
The First Affiliated Hospital of Zhejiang Chinese Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: (1) Patients scheduled for gynecological laparoscopic surgery under general anesthesia, classified as ASA physical status I or II. (2) Patients were aged >=18 years and <65 years.
Exclusion criteria
Exclusion criteria: (1) pre-operative non-pharmacological prophylactic interventions, such as acupoint stimulation ; (2) a body mass index (BMI) >30 kg/m^2 or <18.5 kg/m^2; (3) patients with malignant tumors; (4) pregnant patients; (5) patients experiencing nausea or vomiting within 24 hours prior to surgery; (6) patients with permanent pacemakers or metallic implants; (7) patients with an anticipated anesthesia duration exceeding 4 hours or less than 60 minutes; (8) patients with metal contact allergies; (9) patients with a hemoglobin level below 9g/L; (10) patients refusing to participate in the study; (11) patients with intraoperative blood loss exceeding 400ml or requiring reoperation due to postoperative abdominal hemorrhage; (12) patients with skin damage at the wrist where the device was to be placed; (13) patients who received antiemetic drugs preoperatively. (14) epileptic patient.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the incidence of 24h postoperative nausea and vomiting;Postoperative opioid consumption;Postoperative side effects of acupoint stimulation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction on Nausea and Vomiting 24 Hours After Surgery; | — |
Countries
China
Contacts
Public ContactGuo Xiaowen
The First Affiliated Hospital of Zhejiang Chinese Medical University
Outcome results
None listed