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临床试验/ITMCTR2200006465
ITMCTR2200006465尚未招募1 期

Clinical efficacy evaluation of taVNS for patients with IBS-D

Wangjing Hospital, Chinese Academy of Traditional Chinese Medicine0 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

  • To be admitted to the study, patients must meet all six of the following criteria:
  • (1) The case met the above western diagnostic criteria;
  • (2) Blood routine, urine routine, stool routine plus occult blood, biochemical and imaging tests to exclude other serious chronic diseases;
  • (3) male and female patients aged 18 to 65 years;
  • (4) Course of disease > 6 months;
  • (5) No drug treatment was given within 4 weeks before enrollment;
  • (6) Patients and their family members shall be informed and sign informed consent.

排除标准

  • Patients meeting 1 or more of the following criteria should be excluded:
  • (1) patients with severe liver and kidney function injury, severe heart, brain and lung diseases and severe mental diseases;
  • (2) patients aged under 18 years or over 65 years;
  • (3) during the observation period, taking other drugs, such as opioid antidiarrheal drugs or selective 5-HT reuptake inhibitors, affected the observation results;
  • (4) Subjects are unwilling to participate in the test or have poor compliance;
  • (5) pregnant or lactating women;
  • (6) Patients with other body surface electrical stimulation or acupuncture therapy involved in the original treatment plan.
  • (7) Patients with ear ulceration and other skin lesions.
  • (8) Patients with known hypersensitivity to trimebutin maleate.

研究者

发起方
Wangjing Hospital, Chinese Academy of Traditional Chinese Medicine

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