CTRI/2023/03/051058尚未招募4 期
A Single Centric, Open-Label, Non-Randomized Phase IV Post- Marketing Surveillance Study to Measure the Efficacy and Safety of Product PETSAFFA Tablets in Subjects Suffering from Constipation, Gas and Acidity.
Divisa Herbals Pvt. Ltd.0 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
- 4 期
- 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.Age Between 18 and 80
- •2.Subjects suffering from Constipation, Gas and Acidity
- •3.Subjects willing to sign ICF
- •4.Subjects willing to refrain taking any other similar medication during the study period.
排除标准
- •1.Pregnant, breast-feeding subjects undergone any surgery and else take taken part in any clinical trial.
- •2.Participation in any other clinical study (device or drug) within 30 days prior to Screening.
- •3.Subjects with clinically significant serious cardiovascular, cerebrovascular, respiratory, hepatic, renal disease, congenital or any other disorder
- •4.Subject with abnormal lab values detected at the time of screening shall be excluded.
- •5.A known history or present condition of allergic response to pharmaceutical products its components or ingredients in the investigational product.
- •6.Pre-existing systemic disease necessitating long-term medications.
- •7.Genetic and endocrinal disorder.
- •8.Not willing to sign the ICF or give the consent.
研究者
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