Comparison of MR Enteroclysis and MRI With Per Oral Contrast Using a 6 % Mannitol Solution.
Sponsor
University of Oslo (Other)
Overall Status
Unknown status
CT.gov ID
NCT00204165
Collaborator
(none)
40
1
7
5.7
Study Details
Study Description
Brief 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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Study Design
Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
MRI of the Small Bowel. Comparison of Different Techniques and Contrast.
Study Start Date
:
Nov 1, 2004
Study Completion Date
:
Jun 1, 2005
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Ulleval Universitets sykehus | Kirkeveien 166 | Oslo | Norway | 0407 |
Sponsors and Collaborators
- University of Oslo
Investigators
- Study Director: Nils-Einar Kløw, Prof. MD, Ulleval Universitetssykehus
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00204165
Other Study ID Numbers:
- 431-04150
First Posted:
Sep 20, 2005
Last Update Posted:
Sep 11, 2006
Last Verified:
Sep 1, 2006
Additional relevant MeSH terms: