About this trial

This study is a randomized controlled trial to assess the clinical utility of gallium-68 pentixafor PET/CT in the management of primary aldosteronism (PA). We aim to evaluate whether the addition of 68Ga-pentixafor PET/CT to standard adrenal venous sampling (AVS) improves surgical outcomes in patients with unilateral PA.

Eligibility criteria

Qualifiers

Age ≥19 years

Diagnosed with PA per 2016 Endocrine Society guidelines

Underwent adrenal CT

Signed informed consent

Disqualifiers

Women who are pregnant, breastfeeding, or may become pregnant

Individuals who refuse to undergo surgery

Individuals for whom 68Ga-Pentixafor PET/CT, 11C-Metomidate PET/CT, or adrenal venous sampling (AVS) is not feasible or is refused due to underlying conditions

Individuals who refuse or experience adverse effects from dexamethasone premedication required for 11C-Metomidate PET/CT

Trial design

Treatments tested in this trial

  • 68Ga-pentixafor PET/CT

Treatment groups

90 Participants
are divided into 2 treatment groups

Locations

2
Samsung Medical Center06351, SeoulGangnam-gu, South Korea
Seoul National University Hospital03080, SeoulJongno-gu, South Korea

Sponsors and collaborators

Seoul National University Hospital

Lead sponsor

Samsung Medical Center

Collaborator