Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
15 participants
INTERVENTIONAL
2013-03-31
2016-03-31
Brief Summary
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Detailed Description
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A better understanding of the modes of action of these drugs is required, in order to provide better treatment for chronic constipation. This is somewhat challenging; partly because techniques available to study intestinal contents are limited, and some are unpleasant for the patients. The GI MRI group at the University of Nottingham has recently developed a non-invasive, patient friendly MRI technique for studying the colon. The technique allows assessment of colonic volumes, the response to meals, motility of the colon and transit time of ingested meals. This technique has been used to demonstrate the laxative effect of mannitol and its subsequent reversal with loperamide.
Using MRI, water provides a bright image on T2-weighted images in the small bowel, but the signal is rapidly lost once it reaches the colon. Pilot studies suggest that ispaghula; which is highly hygroscopic and can form a 1.5% gel with water, is able to maintain water in a form which produces bright images on T2-weighted scanning of the colon. The GI MRI group now want to confirm this pilot data by performing a placebo controlled trial of ispaghula husk in healthy volunteers, with the aim of further understanding the mode of action of bulking agents and further improve understanding of MRI parameters when applied to the colon. The aims will be achieved by performing a dose-finding mechanistic study in healthy volunteers, assessing their response to a test meal while taking either placebo, or 2 different doses of ispaghula. Stools will be collected, assessed for water content and compared to water content assessed from T2 weighted MRI. The studies will validate the current technique, optimise current MRI parameters and provide insights into the modes of action of ispaghula.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
DOUBLE
Study Groups
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7 g Ispaghula
Volunteer will take 7 g of ispaghula 3 times daily for one week
7 g Ispaghula
7 g placebo
Volunteer will take 7 g of a placebo 3 times a day for one week
7 g placebo
3.5g ispaghula + 3.5 g placebo
Volunteers will take 3.5 g of ispaghula with 3.5 g placebo 3 times daily for one week
3.5g Ispaghula + 3.5 g placebo
Interventions
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7 g Ispaghula
7 g placebo
3.5g Ispaghula + 3.5 g placebo
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Male or female
* Body mass index (BMI) between 18.0 and 30.0 kg m-2
* Suitable for MRI scanning (eg absence of metal implants, infusion pumps and pacemakers as assessed by the MRI safety questionnaire
* No known gastrointestinal disease
* Not currently smoking
* No strenuous exercise greater than 10 hours per week
* No consumption of more than 21 units of alcohol in a typical week
* No reported participation in another nutritional or biomedical trial 3 months before the pre-study examination or during the study.
Exclusion Criteria
* Antibiotics in the 3 weeks before the pre-study examination
* Pre-existing condition making the need for antibiotics likely during the study
* Previous gastrointestinal surgery (excluding cholecystectomy and appendectomy)
* Known inflammatory bowel disease; coeliac disease
* Subjects considered by the investigator unlikely to comply with study protocol
* Regular (\>3 times/week) use of Probiotics in the 3 weeks prior to, or during the study
18 Years
65 Years
ALL
Yes
Sponsors
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Ironwood Pharmaceuticals, Inc.
INDUSTRY
University of Nottingham
OTHER
Responsible Party
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Principal Investigators
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Robin Spiller, MD, FRCP
Role: STUDY_CHAIR
University of Nottingham
Jeffrey Johnston, MD, FACP
Role: STUDY_DIRECTOR
Ironwood Pharmaceuticals, Inc.
Luca Marciani, Laurea, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Nottingham
Kathryn Murray, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Nottingham
Giles Major, MB BChir
Role: PRINCIPAL_INVESTIGATOR
University of Nottiingham
Ching Lam, MB BCh
Role: PRINCIPAL_INVESTIGATOR
University of Nottingham
Caroline Hoad, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Nottingham
Penny Gowland, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Nottingham
Locations
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NDD BRU and Sir Peter Mansfield Magnetic Resonance Centre
Nottingham, Nottinghamshire, United Kingdom
Countries
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Other Identifiers
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H13122012SCS
Identifier Type: -
Identifier Source: org_study_id
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