Clinical Trial

Acupoint Stimulation Improves Postoperative Wound Pain

Enrolling by Invitation
View on ClinicalTrials.gov →
Record status
This record was last updated May 28, 2025 (before its estimated September 30, 2025 completion). Its status may not reflect the trial's current state.
Summary
Postoperative pain remains one of the most common and distressing symptoms experienced by surgical patients. Poorly managed postoperative pain can impede recovery, reduce patient willingness to mobilize, increase the risk of complications, and negatively affect overall quality of life. Currently, opioids and nonsteroidal anti-inflammatory drugs (NSAIDs) are the primary pharmacological strategies for managing postoperative pain. However, these medications often carry the risk of adverse effects and may not adequately address all aspects of patient comfort and recovery. In response to this challenge, this study aims to evaluate the effects of a non-pharmacological, non-invasive intervention-acupoint stimulation-on postoperative wound pain and mobilization in patients undergoing abdominal surgery. Ultimately, this study seeks to contribute to the development of more diversified and patient-centered pain management strategies, with the expectation that the integration of Chinese and Western medicine will lead to improved patient care and enhanced postoperative recovery.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-05-11.
Trial Details
NCT Number NCT06978335
Lead Sponsor Cheng-Hsin General Hospital
Conditions Abdominal Surgeries, Pain, Acupuncture Points
Enrollment 72 participants
Start Date 2024-06-19
Primary Completion 2025-09-30 (estimated)
Study Completion 2025-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-05-28