Nuclear Imaging for Subtype Diagnosis of Primary Aldosteronism

Status Not yet recruiting

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

Clinical Trial Details

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

View Details

See also
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