A Clinical Follow-up Study on the Efficacy of Thumbtack Needle for Postoperative Sleep and Recovery Treatment
Trial Parameters
Brief Summary
To understand the impact of thumb-tack needle therapy on postoperative sleep and recovery in patients who have undergone general anesthesia, and to explore the clinical significance of thumb-tack needle therapy in improving postoperative sleep quality, preventing postoperative sleep disorders, and promoting postoperative recovery
Eligibility Criteria
Inclusion Criteria: 1. Patients undergoing breast cancer surgery with general anesthesia in the hospital; 2. American Society of Anesthesiologists (ASA) classification I-II; 3. Women aged 18-55 years; 4. No history of chronic insomnia; 5. Individuals who have not taken sedative-hypnotic drugs within the past month. Exclusion Criteria: 1. Those who do not meet the aforementioned inclusion criteria; 2. A history of severe heart, brain, lung, or kidney diseases (such as acute coronary syndrome (ACS), severe heart failure classified as NYHA Class III or IV, severe arrhythmias, severe valvular disease; acute aortic disease, and severe peripheral vascular disease, etc.), or poor physical condition (including reduced exercise tolerance, multi-organ dysfunction, malnutrition, etc.); 3. A history of sleep disorders and psychiatric history; 4. Inability to receive thumb-tack needle treatment.