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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00604266
Other study ID # 07-0216
Secondary ID
Status Withdrawn
Phase N/A
First received January 17, 2008
Last updated May 1, 2017
Start date August 2007
Est. completion date August 2008

Study information

Verified date May 2017
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the feasibility and performance of coregistered 18F-FDG-PET/MRI in the staging of potentially respectable hilar cholangiocarcinoma.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- Hilar cholangiocarcinoma assessed by conventional imaging modalities (triphasic CT scan of the liver) and thought to be potentially resectable.

Exclusion Criteria:

- Biliary drain inserted.

- Contraindication for MRI.

- Pregnant or breast-feeding.

- Uncontrolled diabetes (over 9.7 mmol/L).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Canada UHN - Princess Margaret Hospital Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
University of Toronto University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

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