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临床试验/ITMCTR2200005798
ITMCTR2200005798尚未招募1 期

Clinical study on the prevention and treatment of gastrointestinal dysfunction after lumbar internal fixation by percutaneous acupoint electrical stimulation

Wangjing Hospital, China Academy of Chinese Medical Sciences0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
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
All

入选标准

  • (1) Surgical treatment of lumbar internal fixation under general anesthesia should be performed at an appropriate time.
  • (2) American Society of Anesthesiologists (ASA) Grade I-II.
  • (3) Between the ages of 18 and 65.
  • (4) Normal oral diet, normal exhaust and defecation, and no other serious gastrointestinal diseases before surgery.
  • (5) Good communication skills, able to fully understand and cooperate in completing CRF evaluation.
  • (6) Signed informed consent and volunteered to participate in this study.

排除标准

  • (1)Patients with contraindications to percutaneous electrical stimulation, including stimulated local skin injury or infection, implanted electrophysiological devices.
  • (2) serious dysfunction of heart, brain, lung, liver, kidney and other important system organs.
  • (3) Communication disorders, including language disorders, previous neurological diseases and mental disorders.
  • (4) Severe obesity (BMI>30kg/m2) or severe malnutrition.
  • (5) Long-term use of sedatives, drugs.
  • (6) Erecstool dysfunction caused by severe spinal cord injury or cauda equina nerve injury.

研究者

发起方
Wangjing Hospital, China Academy of Chinese Medical Sciences

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