Skip to main content
OpenTrials
Completed

NCT Number: NCT01805999

Ispaghula and Colonic Water Content

Chronic constipation is a phenomenon which affects nearly 20% of the population worldwide. Bulking agents such as ispaghula are used as treatments, but only half of the patients are satisfied with the treatment. This highlights a need for better treatment options, which requires a deeper understanding of the gastrointestinal fate of the products. The GI MRI Research group at the University of Nottingham has been developing new, non-invasive magnetic resonance imaging (MRI) techniques to image the gastrointestinal tract. In collaboration with Ironwood Pharmaceuticals, the investigators now want to understand the gastrointestinal fate of an ispaghula treatment, and also to improve the understanding of MRI parameters when they are applied to the colon.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NDD BRU and Sir Peter Mansfield Magnetic Resonance Centre

Nottingham, Nottinghamshire, NG7 2RD, United Kingdom

About this study

The Rome III diagnostic criteria for constipation must include two or more of the following symptoms > 25 % of the time: straining, hard or lumpy stools, sense of incomplete evacuation, sensation of anorectal obstruction/blockage, the use of manual manoeuvres to facilitate defecation and fewer than 3 defecations per week. Treatments include osmotic laxatives such as polyethylene glycol and lactulose, stimulant laxatives such as bisacodyl, secretagogues like sodium docusate, and bulking agents such as psyllium.

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.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Apparently healthy; free from GI disorders, aged 18 and 65 years of age
  • 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

  • Inability to discontinue medication likely to alter GI transit
  • 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

Treatment and study plan

7 g Ispaghula

Dietary Supplement

Other names: Metamucil

7 g placebo

Dietary Supplement

3.5g Ispaghula + 3.5 g placebo

Dietary Supplement

Primary outcomes

  1. ascending colon free water content (ACWC)

    Time frame: 0 - 360 minutes

    An assessment of the volume of water in the ascending colon, as obtained from MR images

Secondary outcomes

  1. Ascending, transverse and descending colon volumes

    Time frame: 0 - 360 minutes

    The volumes of each region of the colon will be determined by segmenting MR images

  2. Geometric centres (GC) 24 and 48 hours

    Time frame: t = 24 hours and t = 48 hours

    The geometric centres of 5 transit marker pills will be determined at 24 and 48 hours after ingestion

  3. Small bowel water content

    Time frame: 0 - 360 minutes

    The volume of water in the small bowel will be evaluated from the MR images over the study day

  4. Gastric emptying

    Time frame: 0 - 360 minutes

    The rate of gastric emptying throughout the study day will be determined from MR images

Sponsors and collaborators

Lead sponsor

University of Nottingham

Other

Collaborators

  • Ironwood Pharmaceuticals, Inc.

Registry information

Official study title

Effect of Ispaghula on Colonic Water Content

Important dates

Study start
2013
Primary completion
2013
Study completion
2016
First posted
Mar 6, 2013
Registry last updated
Feb 23, 2017

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.

Published trials that share one or more normalized conditions with this study.