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NCT05636995Active, not recruiting

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

HyperAldosteronism in Pregnancy Predicted Impacts

Source: ClinicalTrials.gov · Last updated 15 Jan 2025

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
25 Oct 2022
Start date
10 Jan 2023
Primary completion date
Mar 2025
Lead sponsor
Université de Sherbrooke
NCT number
NCT05636995

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 10 Jan 2023 to the primary completion date, Mar 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Diagnosed Cushing syndrome

Other

  • Ongoing pregnancy
  • Diagnosed pheochromocytoma
  • Diagnosed secondary hyperaldosteronism

Who the study is looking for

  • Between 4 and 24 weeks post-partum women who had a hypertensive disorder during their latest pregnancy.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hopitalier Universiatire de Sherbrooke
Coordinator of this site? Confirm its status
SherbrookeCanadaUnknown status
Centre Hospitalier Universitaire de Sherbrooke
Coordinator of this site? Confirm its status
SherbrookeCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.