A Clinical Follow-up Study on the Efficacy of Thumbtack Needle for Postoperative Sleep and Recovery Treatment

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-55
SponsorThe First Affiliated Hospital of Xiamen University

About this trial

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

Qualifiers

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;

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

110 Participants
are grouped into 1 trial group

Locations

2
First Affiliated Hospital of Xiamen University361000, XiamenFujian, China
First Affiliated Hospital of Xiamen University361000, XiamenFujian, China

Sponsors and collaborators

The First Affiliated Hospital of Xiamen University

Lead sponsor

Fujian Medical University

Sponsor institution