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

Last updated: December 25, 2024
Sponsor: The First Affiliated Hospital of Xiamen University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Post-surgical Pain

Pain

Chronic Pain

Treatment

N/A

Clinical Study ID

NCT06757023
FirstAHXiamenU-YB-3
  • Ages 18-55
  • All Genders

Study 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

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

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 coronarysyndrome (ACS), severe heart failure classified as NYHA Class III or IV, severearrhythmias, severe valvular disease; acute aortic disease, and severe peripheralvascular disease, etc.), or poor physical condition (including reduced exercisetolerance, multi-organ dysfunction, malnutrition, etc.);

  3. A history of sleep disorders and psychiatric history;

  4. Inability to receive thumb-tack needle treatment.

Study Design

Total Participants: 110
Study Start date:
November 13, 2024
Estimated Completion Date:
November 13, 2026

Connect with a study center

  • First Affiliated Hospital of Xiamen University

    Xiamen, Fujian 361000
    China

    Active - Recruiting

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