ITMCTR1900002709招募中4 期
Postmarket research for two classical formulae of Chinese medicine based on an overarching design
Guangdong Provincial Hospital of 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
- 4 期
- 状态
- 招募中
- 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 70(—)
- 性别
- All
入选标准
- •1 those who meet the diagnostic criteria for IBS-D in Rome IV;
- •2. those who meet the diagnostic criteria of Chinese medicine pattern of dampness;
- •3. aged 18 to 70 years;
- •4. initial IBS-SSS score > 75;
- •5. basic the ability of reading comprehension;
- •6. patients have informed consent and signed informed consent.
排除标准
- •1. patients with heart, liver, kidney, hematopoietic system and other serious diseases and tumors, have a history of nervous system and mental illness;
- •2. patients with warning signs (weight loss within 3 months of emaciation > 10%), hematochezia that is confirmed not to be caused by hemorrhoids or anal fissure , diarrhea at night, fever, family history of colorectal cancer (or polyposis syndrome), inflammatory bowel disease (IBD) or celiac disease.
- •3. organic diseases of the digestive system, or systemic diseases that affect digestive tract dynamics;
- •4. patients with a history of abdominal surgery (except caesarean section);
- •5. those who are unwilling or unable to stop using drugs that affect the effectiveness evaluation of interventions during the study;
- •6. pregnant and nursing women or women planning pregnancy within 3 months;
- •7. those who have participated in other clinical trials in the past 3 months;
- •8. standard points of SAS.>50, standard points of SDS.>53;
- •9. ALT or AST is 2 times higher than the upper limit of normal range., TBIL or BUN is 1.5 times higher than the upper limit of normal range.
- •10. patients with a history of drug allergy used in the study;
- •11. researchers believe that patients are not suitable for this study.
研究者
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