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Trials / Enrolling By Invitation

Enrolling By InvitationNCT07181213

Genetic Predisposition to High Blood Pressure

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
76 (estimated)
Sponsor
Linkoeping University · Other Government
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

Primary aldosteronism (PA) is a known but underdiagnosed cause of high blood pressure. It is estimated that more than 10% of all people with high blood pressure (HT) suffer from PA, which is often caused by aldosterone-producing adrenal cortical tumors (APAs). In a pilot study with 35 patients with APAs leading to hypertension, the investigators have identified a genetic variant in a presumed Calcium-channel gene. The variant was significantly overrepresented in patients with APAs compared to the normal population (12% compared to approximately 4%). Interestingly, all patients having APAs and the variant were men. The SCAPIS study is a world-unique Swedish research study in the field of heart/lungs, in which 30,000 randomly selected people between the ages of 50-64 participated. The study is a collaboration between the universities of Gothenburg, Lund, Linköping, Uppsala and Umeå, as well as the Karolinska Institute in Stockholm. In Linköping, about 5,000 persons participated. The investigators have now screened 4762 persons from the SCAPIS study for this variant and found it in little less than 6%. Overall, patients with the variant had more often been diagnosed with HT and were mote often treated for HT as well. Interestingly, this difference was only found in men. The investigators now want to investigate the following: 1. identify those persons with the genetic variant and HT that have PA, 2. identify those persons with PA that have APAs/unilateral disease, 3. identify how many patients with APAs/unilateral disease can be cured by surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREAdrenalectomySurgical removal of patients with unilateral primary aldosteronism in patients selected by the presence of a genetic variant and hypertension

Timeline

Start date
2026-01-01
Primary completion
2027-06-30
Completion
2027-12-31
First posted
2025-09-18
Last updated
2026-02-02

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT07181213. Inclusion in this directory is not an endorsement.