跳至主要内容
临床试验/ITMCTR2000004043
ITMCTR2000004043已完成1 期

The impact of Transcutaneous Acupoint Electrical Stimulation on high risk patient of Postoperative Nausea and Vomiting: Randomized, double-blind and controlled trial

The First Affiliated Hospital of Chongqing Medical University0 个研究点开始时间: 待定最近更新:
适应症

试验速览

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 65(—)
性别
Female

入选标准

  • female patients undergoing bariatric surgery under general anaesthesia, ASA physical status class II or IV, aged below 65 years, written informed consent was obtained.

排除标准

  • 1. Contraindications for transcutaneous electrical acupoint stimulation (TEAS), such as rash or local infection over the acupoint stimulation skin area, and implantation of a cardiac pacemaker or defibrillator;
  • 2. communication difficulty, included psychiatric or neurological disease;
  • 3. any pre-using medicine or pre-existing medical condition that limited objective assessment before operation, included use of antiemetics, opioids or glucocorticoids, and gastroesophageal reflux;
  • 4. invovled other study within three months of this study beginning.

研究者

相似试验