postoperative sleep
Conditions
Interventions
negative control group:electrical stimulation at percutaneous non-acupoint
Sponsors
Department of Anesthesiology, Tangdu Hospital, Air Force Military Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Female patients undergoing breast cancer surgery; 2. BMI 18-30 kg/m2; 3. Aged 18-65 years; 4. ASA grade I-II; 5. Patients who agreed to sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients who experience the breast cancer surgery; 2. Patients with history of metastases of other organs clearly diagnosed by imaging or pathology; 3. Patients with diagnosed sleep disorder or having sleep problems for more than 3 months; 4. Patients who take psychotropic or other medications that may interfere with sleep within 3 months before surgery; 5. Patients who unable to complete the sleep assessment scale independently; 6. Patients with contraindication on transcutaneous electrical acupoint stimulation iucluding damage or infection at the local skin, electrophysiological device implantation and so on; 7. Patients with acupuncture, transcutaneous electrical acupoint stimulation or similar treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of sleep disorder; | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS pain grade;Incidence of postoperative nausea and vomiting;Incidence of local discomfort after electrical stimulation; | — |
Countries
China
Contacts
Public ContactChangjun Gao
Tangdu Hospital, Air Force Military Medical University
Outcome results
None listed