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CompletedNCT00587210Updated Jan 22, 2016

Evaluation of a New Oral Contrast Agent for MR Enterography in the Assessment of Crohn Disease in the Small Bowel

An observational study in Crohn Disease, sponsored by Mayo Clinic. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-01-22.

Sponsored by Mayo Clinic · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
34
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to assess the exam quality and accuracy of MR using a new oral contrast agent for the evaluation of Crohn Disease in the small bowel.

Read the detailed description

Crohn Disease is an inflammatory condition that involves the small bowel. Patients usually undergo multiple imaging exams in the diagnosis and surveillance of the disease. CT has been shown to have excellent results for detecting active inflammation. In the United States MR has lagged behind CT in utilization for imaging the small bowel. An advantage of MR over CT is the lack of radiation exposure to the patient. A new oral contrast agent is available that provides good distension of the small bowel and allows improved identification of active inflammation. The purpose of this study is to compare the accuracy of MR to CT using this new oral contrast agent and to assess exam quality.

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Conditions studied

  • Crohn Disease

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Keywords

  • Crohn Disease
  • Inflammatory Bowel Disease
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In context

Crohn Disease

1,880 studies on the registry are indexed under Crohn Disease; 462 are open to participants now.

This study's enrollment of 34 is below the median of 162 across 608 observational studies indexed under Crohn Disease.

Browse Crohn Disease studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Gastroenteroloy Clinic; Inflammatory Bowel Disease Clinic

Inclusion criteria

  • Known or suspected Crohn Disease
  • Undergoing colonoscopy and CT enterography

Exclusion criteria

Exclusion Criteria:

  • Contraindication to MR
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
34 participants (actual)

Groups and cohorts

  • Suspected or known Crohn Disease

    Suspected or known Crohn Disease

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What researchers measure

Primary outcomes

  1. exam quality

    Time frame: one time point

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Study locations

1 site
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 22, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00587210
Lead sponsor
Mayo Clinic
Responsible party
Jeff Fidler (Professor of Radiology College of Medicine, Mayo Clinic) — Principal investigator
First posted
Jan 7, 2008
Start date
Jun 2004
Primary completion
Dec 2008
Completion
Dec 2008
Last update
Jan 22, 2016

Study contacts

Jeff L Fidler, MD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2016. You cannot join it, but the record below documents what was studied.

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