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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00205062
Other study ID # M-2004-0251
Secondary ID
Status Terminated
Phase Phase 4
First received September 13, 2005
Last updated October 1, 2015
Start date October 2004
Est. completion date August 2008

Study information

Verified date September 2008
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The main hypothesis is that PET-CT will be a valuable diagnostic tool in diagnosing and evaluating treatment for IBD.


Recruitment information / eligibility

Status Terminated
Enrollment 0
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient with either Crohn's disease or ulcerative colitis whose disease is flaring

Exclusion Criteria:

- Indeterminate diagnosis, pregnant, breastfeeding, or other contraindication to PET-CT

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
PET-CT


Locations

Country Name City State
United States University of Wisconsin Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Does this technique provide an accurate assessment of disease inflammation compared to standard clinical markers?
Secondary Does this technique provide additional information for practitioners on extent of disease?
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