Condition: Postoperative Gastrointestinal Dysfunction (POGD) · Sponsor: The First Affiliated Hospital of Xiamen University
The purpose of this clinical trial is to understand the effect of percutaneous acupoint electrical stimulation on postoperative gastrointestinal dysfunction. It will also investigate the safety of percutaneous acupoint electrical stimulation. The main questions that this trial aims to answer are: Can percutaneous acupoint electrical stimulation alleviate postoperative gastrointestinal dysfunction? Through which mechanisms do they function? Participants will: Preoperatively, patients were either given or not given percutaneous acupoint electrical stimulation. Record their symptoms and biological indicators within 5 days after the operation.
This description comes directly from the study's public registry record.
Linhong Wang · +86-13807548496 · 2797424071@qq.com
Always discuss trial participation with your own doctor first.
| The First affiliated Hospital of Xiamen University | Xiamen, Fujian, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07133620