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临床试验/NCT01398020
NCT01398020已完成不适用

Oral 2L Bi-PegLyte Versus 4L PegLyte Regimen for Outpatient Colonic Preparation: A Randomized, Non-Inferiority Open Trial

University of British Columbia1 个研究点 分布在 1 个国家目标入组 318 人开始时间: 2011年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
318
试验地点
1
主要终点
Difference in Boston Bowel Preparation Scale between the two groups

研究概览

简要总结

The investigators wish to compare the efficacy and patient tolerability of a preparation consisting of 2L Bi-Peglyte plus 15mg of bisacodyl vs the standard preparation of 4L Peglyte. The investigators hypothesize that 2L Bi-Peglyte with 15mg bisacodyl will show higher efficacy and tolerability.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Investigator)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 19 or older
  • Outpatient colonoscopy

排除标准

  • constipation

研究组 & 干预措施

Standard bowel prep

Active Comparator

Subject will receive standard bowel prep prior to colonoscopy.

干预措施: Standard Bowel Prep (Drug)

2L Bi-Peglyte

Experimental

Subjects will be asked to take 2L Bi-Peglyte + 15mg bisacodyl for bowel prep the day before colonoscopy.

干预措施: 2L Bi-Peglyte Bowel Prep (Drug)

结局指标

主要结局

Difference in Boston Bowel Preparation Scale between the two groups

时间窗: 30 minutes

This is an established rating scale to evaluate the quality of bowel prep. The ratings will be compared between the two groups.

次要结局

  • Difference in the number of participants who develop distress symptoms from bowel prep (and the type) between the two groups(20 hours)
  • Difference in the absolute number/percentage of participants in the two groups who find the bowel prep experience easy, acceptable, difficult, very difficult, or unable to complete.(20)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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