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临床试验/NCT01978509
NCT01978509终止不适用

The Affect of Low-Volume Bowel Preparation for Hospitalized Patients Colonoscopies

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2013年9月最近更新:
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适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
Mayo Clinic
入组人数
32
试验地点
1
主要终点
Bowel Cleansing
研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to compare the efficacy of a low-volume bowel preparation versus a high-volume bowel preparation for bowel cleansing on hospitalized patients undergoing colonoscopies.

研究设计

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

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Low volume prep (Prepopik)

Active Comparator

Low volume prep for colonoscopy (Prepopik)

干预措施: Low volume prep (Prepopik) (Drug)

Moderate volume prep (Moviprep)

Active Comparator

Moderate volume prep for colonoscopy (Moviprep)

干预措施: Moderate volume prep (Moviprep) (Drug)

High volume prep (Golytely)

Active Comparator

High volume prep for colonoscopy (Golytely)

干预措施: High volume prep (Golytely) (Drug)

结局指标

主要结局

Bowel Cleansing

时间窗: 24 hours

Measured using the total Boston Bowel Prep Score (BBPS) obtained by adding scores from each segment for a range of minimum 0 = very poor and maximum 9 = excellent.

次要结局

  • Cancellation or Delay of Procedure Due to Poor Bowel Preparation(24 hours)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Francisco C. Ramirez, M.D.

MD

Mayo Clinic

研究点 (1)

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The Affect of Low-Volume Bowel Preparation for... | 临床试验