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

Sponsors and collaborators

The First Affiliated Hospital of Xiamen University

Lead sponsor

Fujian Medical University

Sponsor institution