Anesthesiology
Conditions
Interventions
Control group:Wear a transdermal acupoint electrical stimulation wristband with the same appearance, but only wear it without providing electrical stimulation (false stimulation).
Trial Group:Wear the transcutaneous acupoint electrical stimulation wristband and provide the set effective electrical stimulation
Sponsors
Inner Mongolia Erdos Central Hospital
Eligibility
Sex/Gender
Female
Age
25 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. Single fetus, first cesarean section; 2. Age: 25-35 years old 3. ASA physiological status classification I-II; 4. The Apfel PONV risk score is 2 to 4 points. 5. Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Preoperative use of antiemetic drugs; 2. Presence of preeclampsia or other hypertensive disorders of pregnancy; 3. Abnormal liver or kidney function, coagulation disorders; 4. Allergy to bracelet material (rubber, metal) or skin damage/infection at the wearing site; 5. Presence of a cardiac pacemaker or other metallic internal fixation devices; 6. Inadequate epidural anesthesia requiring change of anesthetic method.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of PONV within 24 hours postoperatively; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative nausea severity (NVAS score);Plasma Serotonin Concentration ;Postoperative sleep quality (using the Richards Campbell Sleep Questionnaire RCSQ);The number of compressions of the patient-controlled analgesic pump (PCA); | — |
Countries
China
Contacts
Public ContactLi Wei
Erdos Central Hospital of Inner Mongolia Autonomous Region
Outcome results
None listed