Postoperative sleep disturbances
Conditions
Interventions
Control group:sham-tACS group
Experimental group:active-tACS group
Sponsors
The First Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1) Age 18~65 years old; 2) patients with ASA classification I-?; 3) Patients undergoing elective gynecological laparoscopic surgery.
Exclusion criteria
Exclusion criteria: 1) Pittsburgh Sleep Quality Score PSQI=7; 2) Contraindications to transcranial electrical stimulation (implantation of electronic devices (such as pacemakers or other metal devices) in the body, cavities or cracks in the skull, or local skin damage or inflammation); 3) History of neurosurgery, epilepsy or psychiatric disorders; 4) Those who have been taking sedative and sleeping pills for a long time; 5) History of severe cardiovascular disease or severe liver and kidney insufficiency; 6) Pregnant and lactating women; 7) BMI=40; 8) Patients who are allergic to the drugs required in the study or refuse to use the intravenous self-controlled analgesic pump; 9) Patients who refuse to sign the informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of sleep disturbance on the first postoperative day; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of sleep disturbance on postoperative day 3;Postoperative resting and active NRS pain scores;Preoperative and postoperative anxiety and depression scores HAD in the two groups;;Postoperative quality of recovery score, QoR-15;Postoperative adverse reactions; | — |
Countries
China
Contacts
Public ContactJianjun Yang
The First Affiliated Hospital of Zhengzhou University
Outcome results
None listed