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Gastrointestinal Motility in Severe Ulcerative Colitis Obtained by Motilis-3D-transit

Gastrointestinal Motility in Patients Suffering From Severe Ulcerative Colitis Obtained by Motilis-3D-transit

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01745029
Enrollment
20
Registered
2012-12-07
Start date
2013-04-30
Completion date
2015-03-31
Last updated
2014-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ulcerative Colitis

Keywords

Gastrointestinal Motility, Inflammatory Bowel Disease, Transit time

Brief summary

The purpose of this study is to describe gastrointestinal (GI) motility in patients suffering from severe Ulcerative Colitis (UC) and to compare these results with similar results obtained in remission. The study is done with the use of Motilis 3D-Transit system which consists of a small electronic capsule ingested and detected by a receiver carried by the patient. Position and orientation of the capsule are interpreted by dedicated computer software and transit times, progression velocity and contraction frequencies can be revealed. The study is mainly descriptive and is designed to test and evaluate the usefulness of the Motilis 3D Transit system in UC patients and to tell investigators more about GI motility during and after severe inflammation. Motilis 3D-Transit system gives investigators a unique chance to study the gastrointestinal canal as a whole during and after severe illness. The investigators expect to include 20 patients suffering from severe UC admitted to Hospital with the purpose of getting medical treatment. The investigators do not expect any drop out, but in case of drop out a new patient will be included.

Interventions

DEVICEMotilis-3D-transit

Sponsors

Motilis Medica A/S ,Switzerland
CollaboratorUNKNOWN
University of Aarhus
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Severe Ulcerative colitis (modified Truelove and Witt score) * Signed informed consent obtained * Fasted since midnight

Exclusion criteria

* Known GI related symptoms complaints or GI diseases * Swallowing disorders * Cancer or other life threatening diseases or conditions * Pregnancy or breast-feeding * Previous abdominal surgery * Abdominal diameter \>140cm? * Drug abuse or alcoholism * Irregular bowel movements * Known cardiovascular or pulmonary diseases * Participation in any clinical study within the last 30 days * Cardiac pacemaker or infusion pump or any other implanted or portable electro-mechanical medical device. * Medication affecting GI motility * MRI within the next four weeks

Design outcomes

Primary

MeasureTime frame
Velocity of progression through the inflamed part of the colon in severe UC compared to the velocity of progression in the corresponding colonic segment in quiescent UC.Three days from baseline visit

Secondary

MeasureTime frame
Velocity of progression through the non-inflamed colonic segments in severe UC compared to the velocity of progression in the corresponding colonic segments in quiescent UC.Three days from baseline

Other

MeasureTime frame
Velocity of progression through the colonic segments in quiescent UC compared to the velocity of progression in the corresponding colonic segments in healthy volunteers.three days from baseline visit

Countries

Denmark

Contacts

Primary ContactAnneMette Haase, ph.d student
annemette.haase@ki.au.dk+45 61658483
Backup ContactKlaus Krogh, Professor
klaukrog@rm.dk+45 2338 5937

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026