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
相似试验
进行中(未招募)
1 期
A study evaluating the of safety and efficacy of LNP023 in patients with a kidney disorder called IgAN nephropathyEUCTR2017-000891-27-DEovartis Pharma AG96
进行中(未招募)
1 期
A study evaluating the of safety and efficacy of LNP023 in patients with a kidney disorder called IgAN nephropathyPrimary IgA NephropathyMedDRA version: 20.0Level: HLGTClassification code 10029149Term: NephropathiesSystem Organ Class: 10038359 - Renal and urinary disordersEUCTR2017-000891-27-SEovartis Pharma AG96
进行中(未招募)
1 期
A study evaluating the of safety and efficacy of LNP023 in patients with a kidney disorder called IgAN nephropathyPrimary IgA NephropathyMedDRA version: 20.0Level: HLGTClassification code 10029149Term: NephropathiesSystem Organ Class: 10038359 - Renal and urinary disordersEUCTR2017-000891-27-GBovartis Pharma AG96
进行中(未招募)
1 期
Study of safety and efficacy of LNP023 in patients with a kidney disorder called IgAN nephropathyPrimary IgA NephropathyMedDRA version: 20.0Level: HLGTClassification code 10029149Term: NephropathiesSystem Organ Class: 10038359 - Renal and urinary disordersEUCTR2017-000891-27-ITovartis Pharma AG100
进行中(未招募)
1 期
A study evaluating the of safety and efficacy of LNP023 in patients with a kidney disorder called IgAN nephropathyPrimary IgA NephropathyMedDRA version: 20.0Level: HLGTClassification code 10029149Term: NephropathiesSystem Organ Class: 10038359 - Renal and urinary disordersEUCTR2017-000891-27-BEovartis Pharma AG100
