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Clinical Trial Summary

This is a prospective study which aims to validate a new diagnostic approach in the tissue characterization of adrenal tumors indeterminate on conventional imaging. For this purpose, it is not necessary to have a control group since the diagnostic accuracy in a well defined subset of patients. Visit 0 : Enrollment, eligibility. Visit 1 : FDG-PET. Visit 2 : Postoperative visit. Visit 3 : 6 months post-PET. Visit 4 : 12 months post-PET.


Clinical Trial Description

Primary objective The primary objective is to assess the diagnostic accuracy of FDG-PET, particularly the SUVmax tumor/liver ratio, in the diagnosis of indeterminate adrenal tumors on conventional imaging. Secondary objectives - To assess the diagnostic accuracy of the tumor SUVmax, and SUVmax of the tumor/mean SUV of the liver. - To evaluate the relationship between SUVmax tumor/liver ratio and Weiss score. - To evaluate the impact of the use of FDG-PET on the treatment options. - To evaluate the economic impact of FDG-PET in the management of indeterminate adrenal tumors (ancillary study). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01284829
Study type Interventional
Source Assistance Publique Hopitaux De Marseille
Contact
Status Completed
Phase N/A
Start date February 4, 2011
Completion date April 5, 2023

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