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Clinical Trial Summary

This study is to evaluate the accuracy of a novel radiopharmaceutical tracer, para-chloro-2-[18F]fluoroethyl etomidate (CETO), used with positron emission tomography (PET) and computed tomography (CT), as a way to subtype unilateral vs. bilateral forms of Primary Aldosteronism, compared to AVS as a reference gold standard.


Clinical Trial Description

This is a phase II study (with targeted recruitment of 30 participants) designed to evaluate the accuracy of a novel radiopharmaceutical tracer, para-chloro-2-[18F]fluoroethyl etomidate (CETO), used with positron emission tomography (PET) and computed tomography (CT), as a way to subtype unilateral vs. bilateral forms of Primary Aldosteronism, compared to AVS as a reference gold standard. Subjects consenting to study participation will receive the [18-F] CETO followed by the PET/CT scan. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05472493
Study type Interventional
Source University of Calgary
Contact Alexander Leung, MD
Phone (403) 955-8358
Email aacleung@ucalgary.ca
Status Not yet recruiting
Phase Phase 2
Start date January 1, 2023
Completion date June 30, 2024

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