ITMCTR1900002644尚未招募1 期
A Multicenter, Randomized and Controlled Trial for Chang-An-Jun-Tai Granule in the Treatment of Patients With Irritable Bowel Syndrome With Diarrhea (IBS-D).
The First Affiliated Hospital of Guangzhou University 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
- 性别
- All
入选标准
- •To simultaneously satisfy the following criteria:
- •1. Conform to the Roman IV(Rome IV) of a patient diagnosed with IBS-D and baseline IBS-SSS score > 75;
- •2. Aged 18 to 60 years;
- •3. Nearly 2 weeks no using the drugs in the treatment of IBS;
- •4. Nearly 2 weeks no using antibiotics or probiotics;
- •5. The patients volunteered to receive the drug and signed an informed consent form, and the informed consent process was in accordance with the relevant provisions of GCP.
排除标准
- •Meet one of the following criteria were excluded:
- •1. there is explanation above the clinical symptoms of the patients with other diseases;
- •2. chronic esophagitis, Barrett esophagus and gastroesophageal reflux disease, peptic ulcer, gastric polyp (without resection), digestive tract tumor patients;
- •3. found that endoscopic gastric mucosa high grade intraepithelial neoplasia, pathological diagnosis, malignant gastrointestinal organic diseases;
- •4. patients with history of abdominal operation;
- •5. allergic or allergic to many medicines;
- •6. confusion, dementia, psychosis, neurosis and various serious unwilling to cooperate;
- •7. with serious the primary cardiovascular disease, liver disease, kidney disease, blood disease, lung disease, autoimmune diseases, or serious diseases affected the survival, such as cancer or aids;
- •8. pregnant and lactating women;
- •9. exist cognitive or other damage (such as vision, etc.) and impact on the participants completed self-report;
- •10. of the pharmaceutical composition ingredients allergies are; is or 4 weeks in other drug clinical trials of patients;
- •11. investigators have sufficient reason to believe that the participants according to current medical or psychological state is not suitable for researchers to study.
研究者
相似试验
进行中(未招募)
不适用
Previous Study | Return to List | Next Study A Trial to Evaluate the Correlation Between Spontaneous Catch-up Growth, Clinical Response to Saizen (Recombinant Human Growth Hormone, r-hGH) and Gene Expression Profiling in Children Small for Gestational Age (SGA) (SAIZEN in SGA)Small for Gestational AgeEUCTR2015-001681-25-Outside-EU/EEAMerck KGaA25
招募中
4 期
A multicenter, randomized, open, controlled trial for the efficacy and safety of Shen-Qi Fu-Zheng injection in the treatment of novel coronavirus pneumonia (COVID-19)ovel Coronavirus Pneumonia (COVID-19)ITMCTR2000003004nion Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology
进行中(未招募)
不适用
A multi-center, randomized, controlled trial with programmed introduction of Sirolimus-based, Calcineurin inhibitor free immunosuppression in recipients of non-heart-beating donor kidney grafts. - PRINS studyEUCTR2007-002763-27-NLErasmus MC
已完成
4 期
A multi-center, randomized, controlled trial with programmed introduction of Sirolimus-based, Calcineurin inhibitor free immunosuppression in recipients of non-heart-beating donor kidney grafts.kidney transplant function10038430NL-OMON31753Erasmus MC, Universitair Medisch Centrum Rotterdam100
尚未招募
1 期
A multicenter, randomized, controlled trial for a novel vaginal microecologic therapy for the treatment of persistent cervical human papillomavirus infection at high riskITMCTR2000003652Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine
