Dental and maxillofacial deformities
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Female patients; 2) Aged 18 to 50 years; 3) Body Mass Index (BMI) ranging from 18.5 to 27.9 kg/m²; 4) Undergoing bimaxillary orthognathic surgery; 5) General anesthesia; 6) American Society of Anesthesiologists (ASA) physical status I to III; 7) After being informed of the study's purpose and content, the patient or their family members signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1) Metal contact allergy; 2) Presence of metallic implants such as a pacemaker, cochlear implant, or other metal-containing devices; 3) Skin damage or scars at the wrist area; 4) History of cranial or mental disorders; 5) History of gastrointestinal surgery or chronic gastrointestinal diseases; 6) Abnormal liver or kidney function; 7) Patients with nausea and vomiting or who have used antiemetic drugs one day before surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of PONV within 24 hours; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain assessment;Number of days in hospital;Electrical stimulation-related complications;The time of first oral intake after surgery;Postoperative patient satisfaction score;The highest PON score at each postoperative time interval ;Incidence of PON, incidence and frequency of POV at each time interval;Incidence of PON, incidence of POV, and rescue antiemetic rate within 24 hours; | — |
Countries
China
Contacts
West China Hospital of Stomatology,Sichuan University