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Clinical Trials in Canada / NCT05636995
Active, not recruiting Observational

HyperAldosteronism in Pregnancy Predicted Impacts (H.A.P.P.I. Trial)

NCT05636995 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2023-01-10
Last updated
2025-01-15

Condition(s) studied

Primary HyperaldosteronismHypertensive Disorder of Pregnancy

Investigational drug(s) / intervention(s)

Aldosterone/Renin Ratio

Aldosterone/Renin Ratio: Blood sample collected to measure the aldosterone/renin ratio for the primary hyperaldosteronism screening.

Study summary

Primary hyperaldosteronism confers a higher risk of cardiovascular complications compared to essential hypertension. Preliminary data is controversial in regards of excessive maternal fetal and neonatal excessive risks in pregnancy.

This study aims at establishing the prevalence of PHA in an population with a recent episode of hypertensive disorder of pregnancy (HDP). The goal is to determine if a universal screening for PHA after a HDP is worthed. The investigators also wish to evaluate the complication rate in pregnant women with PHA compared to women without PHA.

This is a prospective cohort study where all eligible women will be screened for PHA after a HDP episode in the last pregnancy. We will then compare PHA women to non PHA women according to pregnancy complications.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Between 4 and 24 weeks post-partum women who had a hypertensive disorder during their latest pregnancy. Exclusion Criteria: * Ongoing pregnancy * Diagnosed pheochromocytoma * Diagnosed Cushing syndrome * Diagnosed secondary hyperaldosteronism

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Centre Hopitalier Universiatire de Sherbrooke Sherbrooke Quebec
Centre Hospitalier Universitaire de Sherbrooke Sherbrooke Quebec

More Université de Sherbrooke trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05636995 on ClinicalTrials.gov ↗ ← All trials in Canada