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临床试验/TCTR20230523002
TCTR20230523002尚未招募1 期

Efficacy and safety of mild moxibustion in the treatment of diarrhea-predominant irritable bowel syndrome (spleen deficiency and dampness excess syndrome): A study protocol for a randomized controlled trial

ijiang Ji0 个研究点目标入组 92 人开始时间: 2023年5月23日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
92

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • 1.Patients should meet both TCM and Western diagnostic criteria of IBS-D;
  • 2.Patients at age of 18 to 65 years old;
  • 3.No history of relevant treatment before enrollment or with discontinuation of treatment with Chinese medicine, antidiarrheal drugs and antispasmodics for more than 1 month;
  • 4.The total score of the IBS Severity Scoring System score(IBS-SSS) is more than 75;
  • 5.Voluntary participation in this study and signing of the informed consent form.

排除标准

  • 1.Patients with IBS-C, IBS-M, and IBS-U;
  • 2.Patients with inflammatory bowel disease, organic intestinal lesions, peptic ulcer, infectious diarrhea;
  • 3.Patients combined with severe cardiovascular, hepatic, renal, endocrine and hematopoietic system diseases; patients with other diseases other than diarrhea that may affect the test results that cannot be discontinued; patients with mental illness;
  • 4.Patients who are pregnant or lactating, and those who have a birth plan from their enrollment to 1 month after the end of the trial;
  • 5.Those who have participated in other clinical trials within 1 month.

研究者

发起方
ijiang Ji

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