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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00204165
Other study ID # 431-04150
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received September 13, 2005
Last updated September 7, 2006
Start date November 2004
Est. completion date June 2005

Study information

Verified date September 2006
Source University of Oslo
Contact n/a
Is FDA regulated No
Health authority Norway: Directorate of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare MRI enteroclysis with MRI of the small bowel with a per oral 6%mannitol solution.Our hypothesis is that the peroral technique preform the same way as MRI Enteroclysis.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date June 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- above 18 years

- known Crohns disease or strong suspicion.

- need of a small bowel examination

Exclusion Criteria:

- pregnant

- electrolyte disturbances.

- Any MRI contraindications.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms

  • Crohn Disease
  • Magnetic Resonance Imaging, Intestine Small, Crohn Disease.

Intervention

Procedure:
MRI of the small bowel


Locations

Country Name City State
Norway Ulleval Universitets sykehus Kirkeveien 166 Oslo

Sponsors (1)

Lead Sponsor Collaborator
University of Oslo

Country where clinical trial is conducted

Norway,