IRCT20140304016844N3招募中3 期
Comparison of the efficacy of Buspirone and placebo in functional abdominal pain in children
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 100
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
- 6 years 至 18 years（—）
- 性别
- All
入选标准
- •Children from 6 to 18
- •Filling the proposed Rome III diagnostic criteria for functional abdominal pain
- •Having written consent from the parents of these children before their entry to the study
排除标准
- •Using any kind of psychiatric, antibiotic or probiotic medication in last 2 months
- •A history of symptoms improvement following 2 weeks of lactose free diet
- •Positive result in lactose respiratory test
- •Suffering from another digestive disorder or organic disease, in addition to functional abdominal pain
- •Weight of Height below 5 percentile for appropriate age
研究者
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