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临床试验/CTRI/2019/02/017407
CTRI/2019/02/017407已完成3 期

A Double-Blind, Randomized, parallel (adaptive) clinical study to evaluate the efficacy and safety of 3 different types of formulations on bowel function. - Bowel Function Study.

ITC Life Science and Technology center0 个研究点目标入组 229 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
229

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1.Elderly with digestive complaints (Bowel Function)} - Male or Female Age 55-65 years. (E.g. Documented History of Chronic Constipation, IBS, Diarrhea, Stomach pain etc. (For Group â??A )
  • 2. Constipated Subjects (complaints of hard and lumpy stools) â?? Male or Non-pregnant Female Age 18- 50 years ( For Group â?? B )
  • 3. Healthy subjects (as defined by medical history & physical examination)-male or non-pregnant female â?? Age 18- 50 years (For Group C )
  • 4. Rome-III diagnostic criteria prescribed for IBS. (For Group â?? B) (Annexure I)
  • 5.Recurrent abdominal pain or discomfort at least 3 days per month in the last 3 months associated with changes in frequency of stool.
  • 6.Relief of pain or discomfort with defecation. (Group â?? B)
  • 7. Capability to provide written informed consent (For all Groups)

排除标准

  • 1.The subject has a serious, unstable medical condition,such as lung disease,uncontrolled blood pressure,uncontrolled thyroid function,a physical or medical disability or an advanced medical condition.
  • 2.The subject had previous significant gastric or intestinal surgery except appendectomy and gall bladder surgery.
  • 3.IBS sub type other than IBS associated with Constipation.
  • 4.Diarrhea more than 3 bowel movements per day.
  • 5.Antibiotic use within 4 weeks of randomization.
  • 6.Pregnant or lactating women.
  • 7.Subjects on the ongoing therapies with the drugs known to effect gut motility e.g. Laxatives, prokinetics, etc.
  • 8.Subject with eating disorder.
  • 9.History of alcohol, drug, or medication abuse.
  • 10.Participation in another study with any investigational product (IP) within 3 months of randomization.
  • 11.Subject with any condition that might interfere with the conduct of the study as per Investigatorâ??s opinion.
  • 12.Known allergies to any substance in the study product, including lactose intolerance and galactosemia.

研究者

发起方
ITC Life Science and Technology center

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