EUCTR2014-002465-30-IT进行中（未招募）1 期
Spontaneous study on the efficacy and safety of an oral viscous suspension of budesonide administered to children affected by eosinophilic esophagitis.
Dip. Pediatria UOC Gastroenterologia ed Epatologia Pediatrica0 个研究点开始时间: 2014年6月24日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（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 clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •patients of both gender aged below 18 yrs with diagnosis of eosinophilic esophagitis verified by histological examination of esophageal biopsies (eosinophil count >/= 15/HPF)
- •Newly diagnosed patients or previously put under restricted diet or treated with fluticasone/budesonide nebulizer suspension with negative results or relapse.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 30
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Age > 18 yrs
- •Patients with concomitant crhonic intestinal pathologies, heart or gut, respiratory or kidney malformations , neurological deficit, uncertain diagnosis of Eosinophilic Esophagitis
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