ITMCTR2000003873已完成1 期
Clinical study on prevention of propofol injection pain by TAES combined with lidocaine
Department of Anesthesiology, the First Affiliated Hospital of Wenzhou Medical University0 个研究点开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
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
- •1. Women aged 18 to 65 years who were selected for painless hysteroscopy;
- •2. ASA grade I-II;
- •3. BMI kg/m2 18-31;
- •4. No contraindication of propofol and lidocaine;
- •5. informed consent to this pre-treatment programme.
排除标准
- •1. meridian points have surgical incision or scar;
- •2. patients with local skin infection at acupoints;
- •3. patients with upper or lower limb nerve damage;
- •4. have a history of spinal surgery;
- •5. other clinical trials in the last four weeks;
- •6. can't understand NRS score;
- •7. patients with history of allergy to lipids, propofol, local anesthetics (lidocaine) and general anesthesia;
- •8. patients with forearm thrombophlebitis or acute and chronic pain syndrome;
- •9. has a history of gastrointestinal ulcers and analgesic and sedative drug abuse;
- •10. Severe mental illness or Patients with dyslexia;
- •11. Patients with chronic pain syndrome, thrombophlebitis, neurological disorders;
- •12. The researchers found it inappropriate to participate in the trial.
研究者
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