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临床试验/NCT00746395
NCT00746395已完成4 期

Randomized, Placebo-controlled Trial of Lubiprostone as a Preparation for Capsule Endoscopy

University of South Alabama1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2008年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
45
试验地点
1
主要终点
Complete Small Bowel Transit

研究概览

简要总结

This investigation is designed to compare lubiprostone and placebo for cleansing and propulsion in preparation for capsule endoscopy.

详细描述

Introduction of small bowel capsule endoscopy made available an unique technique for diagnostic evaluation of the gastrointestinal tract. After esophagogastroduodenoscopy and colonoscopy about 5% of bleeding cases remain unexplained and capsule endoscopy provides small bowel yield. Capsule endoscopy has special application for evaluation of inflammation bowel disease and other small bowel conditions. Several adjuncts are used to enhance the examination by improving cleansing preparation or propulsion. Metoclopramide, tegaserod, simethicone, erythromycin, phosphates and polyethylene glycol (PEG) colon cleansing agents have been tried and some show improved visualization or increased propulsion where more capsules reach to colonic cecum while still recording within the limits of its 8 hour battery. Recently, our group had an observational report of our experience showing that either full bowel cleansing preparation or prokinetics such as metoclopramide or tegaserod enhanced visualization and functioning capsule transit to the colon. Lubiprostone is a novel chloride channel activator that increases intestinal fluid secretion and motility. It is FDA approved and indicated for treatment of chronic idiopathic constipation.

This investigation is designed to compare lubiprostone and placebo for cleansing and propulsion in preparation for capsule endoscopy. The FDA approved 24 mcg constipation dose was chosen because other medications used in similar single dose in our pilot studies appear effective.

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
Double (Participant, Investigator)

入排标准

年龄范围
19 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy volunteers

排除标准

  • Gi disorders, gi surgery, cardiac, renal, or hepatic insufficiency, severe diarrhea

研究组 & 干预措施

lubiprostone 24mcg single dose

Active Comparator

lubiprostone 24mcg single dose po prior to capsule endoscopy

干预措施: Lubiprostone (Drug)

Sugar pill

Placebo Comparator

Placebo (sugar pill) - matched single dose po prior to capsule endoscopy

干预措施: Placebo (Drug)

结局指标

主要结局

Complete Small Bowel Transit

时间窗: 8 hours

Percent of subjects with capsule passage through small bowel

次要结局

  • Small Bowel Transit(Duration of the test - 8 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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