A Clinical Follow-up Study on the Efficacy of Thumbtack Needle for Postoperative Sleep and Recovery Treatment
Recruiting now
Conditions studied: Postoperative Complications, Postoperative Pain, Acupuncture
In brief
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
Key facts
- Study ID
- NCT06757023
- Run by
- The First Affiliated Hospital of Xiamen University
- People needed
- 110
- Starts
- 2024-11-13
- Expected to finish
- 2026-11-13
- Last updated by the study team
- 2025-01-03
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- Those who do not meet the aforementioned inclusion criteria;
- 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.
Where it is running
- First Affiliated Hospital of Xiamen University — Xiamen, Fujian, China (enrolling)
- First Affiliated Hospital of Xiamen University — Xiamen, Fujian, China (enrolling)
Full record on ClinicalTrials.gov
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