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临床试验/CTRI/2023/08/056220
CTRI/2023/08/056220尚未招募Unknown

To Evaluate the Efficacy and Safety of Constipation Relief Syrup meant for improving Bowel Movement Increased Frequency of Defecation and Soft Stool. - NI

sarbottam care limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方

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.Males and females aged >= 18 years.
  • 2.Organic bowel disease will be ruled out by Fecal Immunochemical Test (FIT) and/or colonoscopy.
  • 3.Must have <= 2 bowel movements during a 7-day qualification period.
  • 4.In otherwise good health as judged by a physical examination and laboratory testing.
  • 5.Not taking medications known to affect bowel function in one week before study.
  • 6.Willing to participate in the study by signing the informed consent.

排除标准

  • 1.Hypersensitive to the study medication.
  • 2.Suffering from severe liver, renal or cardiac diseases, and pregnant or breastfeeding women
  • 3.suspicion to metabolic etiologies and organic disorders such as obstructive disorders and neurologic problems.
  • 2.Obstructive ileus. Acute Abdomen, Chronic Amoebiasis
  • 3.Irritable bowel syndrome (IBS) or inflammatory bowel disease (IBD)
  • 4.Unwilling to adhere the study

研究者

发起方
sarbottam care limited

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