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临床试验/CTRI/2020/03/023787
CTRI/2020/03/023787已完成4 期

A Prospective, Open-label, Non-comparative, Multi-centric Active PMS to evaluateefficacy and safety of STOMAFIT ORAL LIQUID containing Liquor Bismuth Ammonium Citrate2.5ml, Belladonna Dry Extract 9mg, Thymol 0.15mg and Menthol 0.2 mg in Gastritis orGastroesophageal Reflux Disease (GERD)

SUNCARE FORMULATIONS PVT LTD0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Pms

入排标准

入选标准

  • 1. Male and female subjects 18-60 years of age
  • 2. Patients having gastrointestinal illness; signs and symptoms confirmed from clinical judgement
  • 3. Patients willing to give informed consent for the Active PMS and willing to comply with all the study procedure and requiremnets

排除标准

  • 1. History of HIV positive patients
  • 2. Chronic heart failure, respiratory failure or chronic liver and renal failure.
  • 3. Patient with active cancer.
  • 4. Female who is pregnant, planning a pregnancy (during the course of the study) or nursing a child
  • 5. Certain medications that may interfere with the study medication (these will be identified by the study Investigator).

研究者

发起方
SUNCARE FORMULATIONS PVT LTD

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