跳至主要内容
临床试验/CTRI/2017/08/009227
CTRI/2017/08/009227已完成2 期

An Open, Prospective, Comparative Study to Assess the Efficacy and Safety of Pudin Hara Pearls & Liquid in the Management of Indigestion

Dabur India Limited0 个研究点目标入组 79 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
79

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

入选标准

  • Subjects suffering from functional dyspepsia i.e. indigestion and its related signs and symptoms such as fullness, bloating, nausea, gassy discomfort, loss of appetite, spasm and pain in the chest or abdomen for at least on two occasions in the preceding week and were having normal hepatic and renal functions (LFT & RFT)

排除标准

  • Subjects with persistent dyspepsia, vomiting, severe epigastric pain unintentional weight loss, iron deficiency anemia, gastro-intestinal bleeding, dysphasia, odynophagia, previous gastric surgery, epigastric mass, suspicious barium meal, peptic ulcer, and NSAID use. Organic deformity or malignancy of the GI tract, significant systemic and psychological condition (s) which may hamper the study proceedings, conditions requiring immediate surgical intervention, known hypersensitivity to study product or ingredient (s), concomitant medications known to adversely interact with study products or their ingredients, alcohol or drug abuse, pregnancy, lactation and females planning to conceive in near future

研究者

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