Hyperaldosteronism

5

Review clinical trials related to Hyperaldosteronism. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluating the Functional Status of the Adrenal Glands With [68Ga]Ga-PentixaFor in Hyperaldosteronism and Hypercortisolism

Background: The adrenal glands are 2 small organs that sit on top of each kidney. They release hormones; these are chemicals that control how the body works. Tumors on or outside the adrenal glands are called functional if they release hormones; they are called nonfunctional if they do not. Doctors who treat adrenal tumors need to know which type a person has. Researchers want to find better ways to learn whether an adrenal tumor is functional. Objective: To see if a new radioactive tracer (\[68Ga\]Ga-PentixaFor) can make it easier to identify functional adrenal tumors with positron emission tomography (PET) scans. Eligibility: People aged 18 years and older with 1 or more adrenal tumors. They must have increased levels of the hormones aldosterone or cortisol. They must also be enrolled in at least 1 other related NIH study (protocols 19-DK-0066, 18-CH-0031, or 09-C-0242). Design: Participants will be screened. They may have imaging scans. Their ability to perform normal activities will be reviewed. Participants will have one PET scan with the study tracer. The tracer will be given through a tube attached to a needle inserted into a vein. Participants will receive the tracer 1 hour before the scan. They will lie still on a bed while a machine captures images of the inside of their body. The scan will take 45 to 90 minutes. Participants heart rate, blood pressure, and rate of breathing will be checked before, during, and after the scan. Participants will have a follow-up visit 3 days after their scan. This visit can be by phone, email, or in person.

Participants needed: 80
Trial details
Phase: Phase 2Age: 18-120Biological sex: AllType: InterventionalSponsor: National Cancer Institute (NCI)Updated: Jun 29, 2026Locations: 1
Eligibility criteria

one or more adrenal masses on CT and/or MRI and biochemical evidence of excess a... [+8]

Positive beta-human chorionic gonadotropin (beta-HCG) serum or urine pregnancy t... [+2]

Status: Recruiting

Superselective Adrenal Arterial Embolization Versus Oral Spironolactone for Treatment of Idiopathic Hyperaldosteronism

Idiopathic hyperaldosteronism (IHA) represents about 65% of primary hyperaldosteronism cases. Although mineralocorticoid receptor antagonists (MRAs) are the standard first-line treatment, they are often limited by adverse effects. Superselective adrenal artery embolization (SAAE) has been utilized for IHA over the last decade, yet comparative studies against MRAs are lacking. The objective of this study is to compare the safety and efficacy of SAAE and MRA to determine the feasibility of SAAE in treating IHA.

Participants needed: 172
Trial details
Age: 15-60Biological sex: AllType: InterventionalSponsor: Chinese Academy of Medical Sciences, Fuwai HospitalUpdated: Jan 9, 2026Locations: 3
Eligibility criteria

Aged from 15 to 60 with no limits in sex; [+3]

Unilateral adrenal hyperplasia; [+6]

Status: Recruiting

CHina Adrenal Venous saMPling InvestigatiON

Primary aldosteronism (PA) is a major cause of secondary hypertension, yet its optimal diagnosis and management remain challenging. This study comprehensively evaluates adrenal venous sampling (AVS), addressing key clinical, technical, and methodological issues, and aims to clarify the relationship between AVS-guided management and long-term clinical and biochemical outcomes to optimize patient care and prognosis.

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chinese Academy of Medical Sciences, Fuwai HospitalUpdated: Nov 26, 2025Locations: 76Duration: 5 Years
Eligibility criteria

Patients with confirmed primary aldosteronism; [+1]

Severe comorbidity, including stroke, myocardial infarction, heart failure, seve... [+5]

Status: Recruiting

Primary Aldosteronism in Western Norway

In this study the investigators aim to identify and include consecutively patients with primary aldosteronism (PA) diagnosed in the Western and Mid-parts of Norway, to describe the characteristics of these patients, to explore the cardiac effects of PA before and after specific treatment, and to identify long-term outcomes after treatment. One subgroup of the PA patients perform echocardiography to assess left ventricular systolic myocardial function before and after treatment. One subgroup of PA patients perform cardiac MRI to assess myocardial mass, myocardial fibrosis and myocardial function in rest and during stress, before and after treatment. For the cardiac MRI substudy, the PA patients are compared with a group of healthy controls, also included in the study. From 2022 onwards, PA patients diagnosed or subtyped with adrenal vein sampling at Oslo University Hospital will additionally be included in the study, thereby providing a national registration of PA patients.

Participants needed: 300
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Haukeland University HospitalUpdated: Nov 8, 2024Locations: 2
Eligibility criteria

Verified diagnosis or strong suspicion of primary aldosteronism [+1]

Active cancer disease at time of inclusion [+3]

Status: Not yet recruiting

China National Study of Adrenal Venous Sampling

This multicenter study intends to combine retrospective analysis and prospective registry to evaluate the success rate and safety of adrenal venous sampling (AVS) via antecubital and femoral approach for patients with primary aldosteronism. The consistency of AVS with pathological results and clinical outcomes, the factors affecting the success of AVS, and the optimal population for AVS will be aslo analyzed in this study.

Participants needed: 1,500
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Chinese Academy of Medical Sciences, Fuwai HospitalUpdated: Jan 9, 2024Locations: 48Duration: 3 Years
Eligibility criteria

Aged from 18 to 65 with no limits in sex; [+2]

Severe comorbidity, including stroke, myocardial infarction, heart failure, seve... [+5]