About this trial
Postoperative sleep disorder is one of the common complications after general anesthesia. Compared to patients of various ages, elderly patients have a much higher incidence of postoperative sleep disturbance. Postoperative sleep disorders can have many adverse effects, including cognitive impairment, altered pain perception, and emotional disorders, which are not conducive to the long-term prognosis of elderly patients. Enhancing postoperative sleep quality in older patients has become a significant public health concern in the current day due to its direct relationship to both maximizing surgical outcomes and enhancing physical health. This study intends to conduct a prospective, randomized controlled, triple-blind clinical trial on use of transauricular vagal nerve stimulation to improve sleep disorders in elderly patients after general anesthesia surgery, aiming to investigate the efficacy of transauricular vagal nerve stimulation in postoperative sleep disorders in elderly patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients undergoing non-craniocerebral surgery under elective general anesthesia
Age ≥65 years old
American society of Aneshesiologists Grade I to III
Sign informed consent
Disqualifiers
Patients who are expected to retain tracheal intubation after surgery
Disturbance of consciousness, mental disorder, inability to cooperate
Expected survival < 3 months
The estimated operation time is < 2 hours
Trial design
Parallel
Treatments tested in this trial
Transauricular Vagal Nerve Stimulation
DeviceTransauricular vagal nerve stimulation
Treatment groups
Trial outcomes
Primary outcomes
Incidence of sleep disorders within 5 days after surgery.
Secondary outcomes
Sleep quality after surgery.
The investigators collected patient-related information on postoperative days 1, 3, and 5 by using the Pittsburgh Sleep Quality Index (total score ranges from 0 to 21, with higher scores indicating poorer sleep quality) and a sleep monitoring bracelet, and analyzed the subsequent data.
Postoperative pain score
The investigators collected information from the patients on the 1st and 2nd postoperative days by Visual Analogue Scale and analyzed the data subsequently. The scale is based on a 10-cm horizontal line drawn on a piece of paper, with 0 cm at one end of the line indicating "no pain at all" and 10 cm at the other end indicating "extreme pain"; the level of pain increases from 0 to 10 cm, with higher scores indicating more intense pain. The higher the score, the more severe the pain.
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