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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06757023

Enrollment

110

Registered

2025-01-03

Start date

2024-11-13

Completion date

2026-11-13

Last updated

2025-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acupuncture, Postoperative Complications, Postoperative Pain

Brief 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

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 55 Years

Healthy volunteers

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 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 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.); 3. A history of sleep disorders and psychiatric history; 4. Inability to receive thumb-tack needle treatment.

Design outcomes

Primary

Measure	Time frame	Description
Pittsburgh sleep quality index(PSQI)	1 day or 2 days before anesthesia exposure and 1, 3, and 7 days after anesthesia exposure.	Total scores range from 0 to 21, with higher scores indicating worse sleep quality.

Secondary

Measure	Time frame	Description
Later Recovery evaluated by QoR-40 questionnaire	QoR-40 score on the third day after surgery	The maximum total score is 200, with higher scores indicating better recovery quality

Countries

China

Contacts

Primary ContactBin Yang doctor

yangbin4332@outlook.com1385998603

Outcome results