跳至主要内容
临床试验/IRCT2013043013183N1
IRCT2013043013183N1已完成2 期

Assessment of effect of Wild Mint product in Postprandial Distress Syndrome

shahed University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
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
18 years 至 65 years(—)
性别
All

入选标准

  • patients with 18-65 old years? Early Satiety? bothersome postprandial fullness? Without Organic Disorders on physical examination and Endoscopic
  • Exclusion criteria: Patients with organic disorders? The use of Chemicals and Herbals any other medication? History of Abdominal surgeries? History of bloody diarrhea? Pregnancy and lactation? Lack of interest in work? Not sign the consent

排除标准

  • 未提供

研究者

发起方
shahed University of Medical Sciences

相似试验