Sleep disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age >= 55 years old, ASA II-III grade, BMI18-25kg/m^2, Hypertensive patients undergoing urological surgery, including various stones and tumors (excluding functional tumors such as pheochromocytoma and primary aldosteronism), without serious systemic diseases, voluntarily participate in this trial and sign an informed consent form.
Exclusion criteria
Exclusion criteria: Preoperative patients with severe heart, lung, brain, kidney, central nervous system, and psychiatric disorders; Patients with a history of using sedatives, painkillers, or antidepressants; Those who are not suitable for transcutaneous acupoint electrical stimulation; Individuals with severe visual or hearing impairments who are unable to communicate; Individuals allergic to the use of anesthetic drugs; Individuals who have undergone other types of surgeries within the past six months; Those who have poor compliance and are unable to cooperate with treatment; The patient or family members do not agree to conduct this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Athens Insomnia Scale Score;Pittsburgh Sleep Quality Index Scale;Non invasive cardiac output;Peripheral vascular resistance; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure and heart rate; Collect relevant data on the preoperative and postoperative sleep monitoring wristbands on day 1 (including all day sleep duration),The duration of sleep, deep sleep time throughout the day, light sleep time throughout the day, wakefulness time, time of falling asleep last night, time of waking up this morning, and based on body movements during sleep. ; | — |
Countries
China
Contacts
The First Affiliated Hospital of Guangxi Medical University