JPRN-UMIN000030884招募中未知
A comparison of remission rate at 8 weeks between combination therapy of Ustekinumab and Budesonide and monotherapy of Ustekinumab in moderate to severe Japanese Crohn's disease; A phase III, single-center, double blind, randomized control trial. - A comparison between combination therapy of Ustekinumab boosted by Budesonide and monotherapy of Ustekinumab for Crohn's disease. (BUUST study)
Tohoku University Hospital, Division of Gastroenterology0 个研究点目标入组 80 人开始时间: 2018年2月20日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 80
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
- 18years-old 至 75years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •With stoma. With surgical lesion such as stenosis or abscess. Inpatient with intravenous hyperalimentation. History of allergy for Ustekinumab or Budesonide. Woman with pregnancy, possibility of pregnancy. Woman who is within 28 days after postpartum, or gives the breast to a child. With psychiatric disorder Within 5 years after diagnosis or treatment of malignant tumor. Patient who has active infection.
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