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UnknownNCT06047912

Screening for Primary Aldosteronism in Hypertension With 24-hour URinary aLdosterone

Status
Unknown
Phase
Study type
Observational
Enrollment
120 (estimated)
Sponsor
Dr Ian B Wilkinson · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is an observational study compares the positivity rates of two tests for screening for primary aldosteronism: plasma aldosterone renin ratio and 24-hour urine aldosterone in patients with young-onset hypertension with or without other clinical features of primary aldosteronism.

Detailed description

Plasma aldosterone and renin measurements are subject to significant intra-individual variability, including variation related to posture, time of day and sodium balance. Aldosterone secretion is not constant and may be subject to diurnal variation. As such one-off testing of ARR, does not consider the salt status of the individual necessitating repetition of tests to ensure false negative or false positive test results are ruled out. The value of accumulated aldosterone in a 24-hour sample has the advantage that it does not depend on circadian variation. This pilot observational study will help establish the positivity rates of both standard plasma aldosterone renin ratio and 24-hour urine aldosterone, and the degree to which they correlate but will help establish if untargeted screening in young-onset hypertension is feasible and test the robustness of current standard guidelines for primary aldosteronism screening and case confirmation.

Conditions

Timeline

Start date
2023-09-15
Primary completion
2024-09-30
Completion
2024-12-30
First posted
2023-09-21
Last updated
2023-09-21

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06047912. Inclusion in this directory is not an endorsement.