Postoperative sleep disturbance
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Before starting trial-related activities, voluntarily sign the informed consent form, fully understand the purpose and significance of this experiment, and voluntarily comply with the trial procedures; 2. Planned elective gynecological laparoscopic surgery under general anesthesia with an expected duration of 1 to 3 hours; 3. Age 18 to 65 years; 4. American Society of Anesthesiologists (ASA) physical status classification I or II; 5. Body mass index (BMI) between 18 kg/m^2 and 30 kg/m^2.
Exclusion criteria
Exclusion criteria: 1. Pittsburgh Sleep Quality Index (PSQI) > 7 points; 2. Preoperative neurological or psychiatric disorders (such as depression, Parkinson's disease, schizophrenia, epilepsy, etc.) or sleep-related disorders (such as obstructive sleep apnea syndrome, etc.); 3. History of brain disease (such as cerebral infarction, cerebral hemorrhage, intracranial lesions, traumatic brain injury, etc.); 4. History of neurosurgery; 5. Cognitive or communication impairments; 6. Long-term use of sedative or hypnotic drugs; 7. Severe liver or kidney dysfunction; 8. Pregnancy or breastfeeding; 9. Refusal to participate in this study; 10. Other conditions judged by the researcher that make the subject unsuitable for participation in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of sleep disorder on the first night after operation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hospital Anxiety and Depression Scale;waking time;Adverse event;Opioid drug consumption;Incidence of sleep disorder on the 2nd, 3rd and 7th night after operation;electroencephalogram;Pain score; | — |
Countries
China
Contacts
The First Affiliated Hospital of Zhengzhou University