Perioperative sleep disorder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Female patients undergoing laparoscopic surgery; 2. Surgical patients aged 18-65; 3. The American Society of Anesthesiologists (ASA) physical status is graded I-III; 4. Body mass index (BMI) 18-30kg/m^2; 5. Good compliance, willing to accept this therapy;
Exclusion criteria
Exclusion criteria: 1. The patient refused to participate in the study. 2. Body mass index (BMI) > 30kg/m^2; 3. Presence of pre-operative conditions that affect sleep, such as neurological disorders, endocrine disorders, psychiatric disorders, or chronic pain that the researchers believe may interfere with the evaluation of the study. 4. Insomnia Severity Index (ISI) >= 8 or other preoperative sleep disorders such as obstructive sleep apnea, periodic limb movement disorder, restless legs syndrome, circadian rhythm disorder, or narcolepsy; 5.A recent history of drug abuse; 6. Presence of cognitive impairment or inability to communicate; 7. Patients with severe complications such as severe allergic reactions or massive bleeding during surgery who require rescue; 8. Use of hypnotic drugs during postoperative follow-up; 9. Do not use patient-controlled intravenous analgesia (PCIA); 10. Failure to complete the study program or to lose patients for various reasons during follow-up; 11. Those with a history of alcoholism or excessive consumption of coffee or strong tea; 12. Participate in other clinical investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence rate of postoperative sleep disorders; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale;Hospital Anxiety and Depression Scale;Incidence rate of postoperative complications; | — |
Countries
China
Contacts
Shaanxi Provincial People's Hospital