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Primary aldosteronism in general practice: organ damage, epidemiology and treatment

Primary aldosteronism in general practice: organ damage, epidemiology and treatment - PAGODE

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37681
Enrollment
1100
Registered
2013-06-21
Start date
2013-08-13
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

high blood pressure primary aldosteronism

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Newly diagnosed hypertensive patients in general practice

Exclusion criteria

Exclusion criteria: Use of antihypertensive medication Heart failure class II, III or IV (according to the New York Heart Association) Pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frame
Part 1: Prevalence of primary aldosteronism in newly diagnosed hypertensive patients in Dutch general practice Part 2: Difference in cardiorenovascular damage in patients with versus without PA, based on a composite of the following parameters: - Left ventricular mass index in g/m2 - Intima-media thickness of carotid artery in mm - Pulse wave velocity in m/s - Central aortic blood pressure in mmHg - Flow-mediated dilation in % - Albuminuria in mg albumin per mmol creatinin Part 3: Difference in reduction of daytime systolic ABPM in patients with normokalemic PA versus patients with essential hypertension in a standardized treatment regimen during conventional antihypertensive therapy

Secondary

MeasureTime frame
Part 2: to observe differences in • Serum potassium • Low density lipoprotein • Total cholesterol to high density lipoprotein ratio Part 3: to observe differences in • Reduction of daytime systolic ABPM in patients with PA versus patients with essential hypertension in a standardized treatment regimen during spironolactone (or eplerenone) • Serum potassium response using conventional antihypertensive medication • Adverse effects using conventional antihypertensive medication • Serum potassium response using spironolactone (or eplerenone) • Adverse effects using spironolactone (or eplerenone)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)