TCTR20180131001已完成3 期
Efficacy of Curcuma longa in treatment of postprandial distress syndrome: an open-label randomized controlled trial
icharat Sawangroj0 个研究点目标入组 78 人开始时间: 2018年1月31日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 78
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
- 20 Years 至 60 Years（—）
- 性别
- All
入选标准
- •- Patients with PDS of functional dyspepsia according to ROME IV criteria including uninvestigated dyspepsia
- •- No alarm features
- •- Discontinued all GI medications for 1 week
排除标准
- •- Drugs allergy (simethicone and/or Curcuma longa)
- •- Pregnancy/lactation
- •- History of gastric malignancy
- •- History of gallstone or biliary obstruction
研究者
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