Ispaghula and Colonic Water Content

NCT ID: NCT01805999

Last Updated: 2017-02-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-03-31

Study Completion Date

2016-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Healthy

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

7 g Ispaghula

Volunteer will take 7 g of ispaghula 3 times daily for one week

Group Type EXPERIMENTAL

7 g Ispaghula

Intervention Type DIETARY_SUPPLEMENT

7 g placebo

Volunteer will take 7 g of a placebo 3 times a day for one week

Group Type PLACEBO_COMPARATOR

7 g placebo

Intervention Type DIETARY_SUPPLEMENT

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

Group Type ACTIVE_COMPARATOR

3.5g Ispaghula + 3.5 g placebo

Intervention Type DIETARY_SUPPLEMENT

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

7 g Ispaghula

Intervention Type DIETARY_SUPPLEMENT

7 g placebo

Intervention Type DIETARY_SUPPLEMENT

3.5g Ispaghula + 3.5 g placebo

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Metamucil

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ironwood Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role collaborator

University of Nottingham

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

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

Explore where the study is taking place and check the recruitment status at each participating site.

NDD BRU and Sir Peter Mansfield Magnetic Resonance Centre

Nottingham, Nottinghamshire, United Kingdom

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United Kingdom

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

H13122012SCS

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Mode of Action of Moviprep
NCT01622972 COMPLETED PHASE4
Fibers and Gut Health
NCT02234518 COMPLETED NA
Fiber and Water Improve Bowel Habit in Humans
NCT02838849 COMPLETED PHASE1/PHASE2
Gastrografin in Postoperative Ileus
NCT01648972 COMPLETED PHASE2/PHASE3
Prucalopride Versus Placebo in Gastroparesis
NCT02031081 COMPLETED PHASE2/PHASE3