RecruitingNCT06757023
A Clinical Follow-up Study on the Efficacy of Thumbtack Needle for Postoperative Sleep and Recovery Treatment
Sponsor
The First Affiliated Hospital of Xiamen University
Enrollment
110 participants
Start Date
Nov 13, 2024
Study Type
OBSERVATIONAL
Conditions
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
Min Age: 18 YearsMax Age: 55 Years
Inclusion Criteria8
- Patients undergoing breast cancer surgery with general anesthesia in the hospital;
- American Society of Anesthesiologists (ASA) classification I-II;
- Women aged 18-55 years;
- No history of chronic insomnia;
- Individuals who have not taken sedative-hypnotic drugs within the past month.
- 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.);
- A history of sleep disorders and psychiatric history;
- Inability to receive thumb-tack needle treatment.
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Locations(2)
View Full Details on ClinicalTrials.gov
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NCT06757023
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