跳至主要内容
临床试验/JPRN-UMIN000024917
JPRN-UMIN000024917尚未招募未知

Clinical Efficacy and Safety of Oral Qing-Dai in Patients with Ulcerative Colitis - Clinical Efficacy and Safety of Oral Qing-Dai in Patients with Ulcerative Colitis

Kumamoto red cross hospital division of gatroenterology0 个研究点目标入组 20 人开始时间: 2016年12月3日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
20

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
7years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • colitis associated dysplasia, symptomatic intestinal stenosis a history of side effect or allergy of Chinese herbal medicine a need for potential surgery after enrollment in this study signs of other types of colitis, severe liver ,heart or renal diseases; or a history of malignant diseases, psychosomatic disorders,infectious disease. Pregnant or breastfeeding women. The patients treated with leukocyte aphaeresis,prednisolone >=40mg,adalimumab,tacrolimus or cyclosporine within 2 weeks before the commencement of the study. The patients treated with infliximab whitin 4 weeks before the commencement of the study. Changing the dose of mesalamine or prednisolone within 2 weeks before the commencement of the study. The patients treated with thiopurine within 12 weeks before the commencement of the study. Changing the dose of thiopurine within 4weeks before the commencement of the study.

研究者

发起方
Kumamoto red cross hospital division of gatroenterology

相似试验