Sleep disorders
Conditions
Interventions
Control group:One night after surgery, give an equal dose of physiological saline nasal spray half an hour before going to bed
Experimental group:One night after surgery, 50 µ g of dexmedetomidine nasal spray was administered half an hour before going to bed
Sponsors
Guangzhou Women and Children's Medical Center
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Women aged 18-60 2. ASA level I-II 3. Accepting gynecological laparoscopic surgery 4. The surgery will end before 5 pm.
Exclusion criteria
Exclusion criteria: 1. Patients with preoperative sleep disorders (Pittsburgh Sleep Quality Index score = 7) 2. Patients with obstructive sleep apnea hypopnea syndrome 3. Those who take sedatives and antidepressants, have drug and alcohol dependence 4. Individuals with a history of mental illness, cardiovascular disease, nasopharyngeal carcinoma, nasal bleeding, and other nasal abnormalities.5. Having severe hearing or visual impairments, unable to communicate effectively, or refusing participants.6 Having a history of serious chronic diseases such as heart, brain, lungs, liver, and kidneys. 7. Individuals who are unable to understand the content of the scale and are allergic to experimental drugs 8. Anesthesia or surgical accidents occur during the operation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep Assessment Scale;Deep sleep duration;Sleep efficiency;Light sleep duration; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hypotension;Bradycardia;Postoperative nausea and vomiting; | — |
Countries
China
Contacts
Public ContactXi Chen
Guangzhou Women and Children's Medical Center
Outcome results
None listed