NCT01678781已完成不适用
Open International Study on Quality of Life in IBS Patients Before and After 8 Weeks Treatment With Mebeverine/Pinaverium Bromide
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Abbott
- 入组人数
- 607
- 试验地点
- 24
- 主要终点
- Change in Irritable Bowel syndrome (IBS) quality of life (QoL) measure (IBS-QoL) to assess the impairment of QoL in IBS patients
研究概览
简要总结
A study to evaluate, by country and overall, the changes from baseline of the irritable bowel syndrome quality of life (IBS QoL) total score after 4 and 8 weeks of treatment with Duspatalin® or Dicetel® in IBS patients.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Irritable bowel syndrome patients diagnosed by Rome III criteria (18 years or older)
排除标准
- •Pregnancy and lactation
- •Specific contraindications to mebeverine hydrochloride or pinaverium bromide
结局指标
主要结局
Change in Irritable Bowel syndrome (IBS) quality of life (QoL) measure (IBS-QoL) to assess the impairment of QoL in IBS patients
时间窗: From baseline up to the week 8 visit
次要结局
- Change in abdominal pain(From baseline up to the week 8 visit)
- Change in bloating(From baseline up to the week 8 visit)
- Change in feeling of abdominal distension(From baseline up to the week 8 visit)
- Change in stool frequency(From baseline up to the week 8 visit)
- Change in stool form(From baseline up to the week 8 visit)
- Change in straining of evacuation(From baseline up to the week 8 visit)
- Change in urgency of evacuation(From baseline up to the week 8 visit)
- Change in feeling of incomplete evacuation(From baseline up to the week 8 visit)
研究者
研究点 (24)
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