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OpenTrials
Completed

NCT Number: NCT00746395

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

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

Completed

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Key information

Age range

19 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

USA Pavilion at Infirmary West

Mobile, Alabama, 36693, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy volunteers

Exclusion criteria

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

Treatment and study plan

Lubiprostone

Drug

24 mcg oral administration

Other names: Amitiza

Placebo

Drug

Oral administration

Other names: Sugar pill

Primary outcomes

  1. Complete Small Bowel Transit

    Time frame: 8 hours

    Percent of subjects with capsule passage through small bowel

Secondary outcomes

  1. Small Bowel Transit

    Time frame: Duration of the test - 8 hours

    Small bowel transit time

Sponsors and collaborators

Lead sponsor

University of South Alabama

Other

Collaborators

  • Sucampo Pharmaceuticals, Inc.
  • Takeda

Registry information

Important dates

Study start
2008
Primary completion
2008
Study completion
2008
First posted
Sep 4, 2008
Registry last updated
Oct 8, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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