Skip to content

Activation of the innate immune system in patients with primary hyperaldosteronism

Activation of the innate immune system in patients with primary hyperaldosteronism - Innate immune activation in hyperaldosteronism

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43020
Enrollment
30
Registered
2016-11-08
Start date
2017-01-02
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

bloedvataandoeningen, arteriosclerose Conn's syndrome primary hyperaldosteronism

Interventions

hyperaldosteronism
inflammation
innate immune system
PET scan

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Patients with PA (primary hyperaldosteronism): - Diagnosis of PA according to current guideline - Age >=18 yrs - Written informed consent;Patients with essential hypertension: - Exclusion of PA according to current guidelines - Age >=18 yrs - Written informed consent

Exclusion criteria

Exclusion criteria: - Treatment with MR antagonists within the 4 weeks before participation - Smoking - Diabetes mellitus - Previous cardiovascular events (stroke, TIA, myocardial infarction) - Heart failure - Auto-inflammatory or auto-immune diseases - Use of immunomodulating drugs - Renal failure (MDRD 35 - Previous vaccination within 3 months prior to study entry. - Current infection or clinically significant infections within 3 months before participation (defined as fever >38.5).

Design outcomes

Primary

MeasureTime frame
Primary study parameter/endpoint: Vascular wall inflammation in the aorta, the left and right carotid artery and the left and right iliac and femoral arteries, as detected with FDG-PET scanning, according to current European guidelines.

Secondary

MeasureTime frame
Secondary study parameters/endpoints: The inflammatory/atherogenic phenotype of circulating monocytes in PA patients. FDG uptake in spleen and bone marrow.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)