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Study identifier: NCT06616142 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Primary Aldosteronism  ·  Sponsor: University Medical Center Groningen

PhasePhase 1/Phase 2
Planned participants12
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

dr. M.N. Kerstens  ·  +31 0503613518  ·  m.n.kerstens@umcg.nl

Merit Schaafsma, MD-PhD candidate  ·  +31503610972  ·  m.schaafsma@umcg.nl

Always discuss trial participation with your own doctor first.

Locations (1)

University Medical Center GroningenGroningen, Provincie Groningen, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT06616142