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
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