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临床试验/NCT04145856
NCT04145856已完成4 期

Efficacy of the Combination Therapy With Alverine-simeticone and i3.1 Probiotic Formula in the Quality of Life of Patients With IBS-D or IBS-M in Hospital Juarez Mexico

Hospital Juarez de Mexico2 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2018年9月3日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
55
试验地点
2
主要终点
Disease-specific quality of life (QoL)

研究概览

简要总结

This randomized study evaluates the usefulness of the I31 probiotic formula, alone or in combination with alverine/simethicone, against placebo, in the treatment of diarrhea-predominant or mixed irritable bowel syndrome

详细描述

Irritable Bowel Syndrome (IBS) is a functional gastrointestinal disease in which recurrent abdominal pain is associated with defecation or a change in bowel habits. Disordered bowel habits are typically present (ie, constipation, diarrhea, or a mix of constipation and diarrhea), as are symptoms of abdominal bloating/distention.

I31 is a probiotic formula composed of strains Pediococcus acidilactici CECT7483 and Lactobacillus plantarum CECT7484 and CECT7485, previously shown to improve quality of life in patients with IBS of Caucasian descent.

Alverine/simethicone is a combination of two drugs: Alverine citrate relaxes muscle cramps that occur in the intestine in conditions such as irritable bowel syndrome and diverticulosis. Simethicone is an antifoam administered orally. Reduces gas formation and facilitates its elimination from the digestive tract

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 59 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects attending Hospital Juarez de Mexico with a diagnosis of diarrhea-predominant or mixed irritable bowel syndrome (IBS-D and IBS-M), according to Rome-IV criteria (Lacy et al. Gastroenterology 2016), providing Informed Consent.

排除标准

  • Unexplained weight loss, blood in feces, anemia.
  • Use of systemic antibiotics, NSAIDs, antipsychotic or prokinetic medication in the 3 weeks before study initiation.
  • Pregnant or lactating women.
  • History of gastrointestinal cancer.
  • Suspicion of coeliac disease, inflammatory bowel disease (IBD), endometriosis or pelvic inflammatory disease.
  • History of abdominal surgery within 2 years (3 months if appendectomy or herniorraphy)
  • BMI below 18
  • Known allergy to any of the components in the treatments

结局指标

主要结局

Disease-specific quality of life (QoL)

时间窗: 6 weeks

Irritable bowel syndrome-specific validated IBSQoL questionnaire (Hahn et al. Aliment Pharmacol Ther 1997). Response is defined as an improvement of 15 or more points in the normalized 0-100 score

次要结局

  • Abdominal Pain(6 weeks)
  • Diarrhea(6 weeks)

研究者

发起方
Hospital Juarez de Mexico
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Nuria Pérez López

Digestive Physiology Lab Head

Hospital Juarez de Mexico

研究点 (2)

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