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Clinical Trials/NCT00731809
NCT00731809
Unknown
Phase 4

Evaluation of PET CT in the Management of Patients With Crohn's Disease.

Rabin Medical Center1 site in 1 country50 target enrollmentApril 2008
ConditionsCrohn's Disease

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Crohn's Disease
Sponsor
Rabin Medical Center
Enrollment
50
Locations
1
Last Updated
17 years ago

Overview

Brief Summary

18F-FDG PET/CT (2-[fluorine-18] fluoro-2-deoxy-D-glucose, Positron emission tomography- CT) is a noninvasive technique that allows quantifying and precisely localizing 18F-FDG uptake in the entire body. 18F-FDG uptake is caused by increased local metabolic activity. Such increased uptake has been described not only in neoplastic lesions but also in inflammatory lesions. In this condition, uptake has been correlated with local stimulation of tumor necrosis factor, and with monocyte priming and activation. A physiologic variable uptake may be observed in the bowel, especially the cecum, and has limited the use of PET in inflammatory bowel diseases. The advantage of combined PET and CT devices lead to significant improvements in the interpretation of the bowel areas, and greatly reduces the number of false-positive findings in the gastrointestinal tract.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
October 2010
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients suspicious for active disease:
  • Patients with suspected but undiagnosed Crohn's disease
  • Patients with serological markers of inflammation (elevated ESR, CRP or thrombocytosis) but clinically in remission
  • Patients with a stricture which might be fibrous in which case surgery is indicated or inflammatory for which medical management is indicated
  • Able to sign a consent form

Exclusion Criteria

  • Pregnancy
  • Breastfeeding
  • Infectious colitis determined at the initial checkup
  • Allergy to iodine contrast

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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