drugset / Trial / NCT06616142

Subtyping Primary Aldosteronism With Para-chloro-2-[18F]Fluoroethyl-etomidate

NCT06616142 ↗

Phase 1/2 Recruiting 12 enrolled University Medical Center Groningen
Non-randomizedSingle-groupOpen-labelDiagnostic

Summary

The goal of this clinical trial is to investigate the uptake characteristics of \[18F\]CETO in adrenal tissue in patients with two different subtypes of primary aldosteronism. The main questions it aims to answer are: * What are the uptake characteristics of \[18F\]CETO in adrenal tissue in patients with primary aldosteronism? * What is the concordance between the adrenal vein sampling and the \[18F\]CETO PET/CT scan results? * What is the effect of adrenal perfusion on \[18F\]CETO uptake in the adrenal glands? Researchers will compare the results of the adrenal vein sampling to a \[18F\]CETO PET/CT scan to see if the PET/CT can accurately identify the subtypes of primary aldosteronism. Participants will: * Take dexamethasone three days prior to the scan * Undergo a \[18F\]CETO PET/CT * Report burden of pre-treatment and PET/CT scan

Timeline

Start
2024-11-06
Primary completion
2026-10
Completion
2027-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator [18F]CETO Diagnostic / imaging agent — —
Comparator Dexamethasone Small molecule — Oral

Indications