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NCT05925569Active, not recruiting

Electronic Alert to Improve Testing For Primary Aldosteronism in Patients With Hypertension

Electronic Alert-Based Computerized Decision Support to Improve Testing For Primary Aldosteronism in Patients With Hypertension: ALERT-PA

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

Primary aldosteronism (PA) is common but rarely recognized cause of hypertension that carries excess cardiovascular and renal risk and has approved targeted treatments. Despite current clinical guidelines that recommend screening in a defined set of high-risk populations, less than 5% of eligible patients are ever screened for PA. This study aims to evaluate the impact of a computer decision support Best Practice Advisory (BPA) alert on rates of screening for PA in guideline-eligible patients, referral to specialist PA care, and treatment with mineralocorticoid receptor antagonists.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
12501 (actual)
First submitted
22 Jun 2023
Start date
13 Mar 2024
Primary completion date
9 Dec 2024
Lead sponsor
Brigham and Women's Hospital
NCT number
NCT05925569

What you commit to

  • Study type: Interventional
  • Participants enrolled: 12501
  • From 13 Mar 2024 to the primary completion date, 9 Dec 2024
  • 1 site 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

  • History of Primary Aldosteronism (ICD Code)

Other

  • Prescription for a Mineralocorticoid Receptor Antagonist (MRA) within the last 3 months

Who the study is looking for

  • Adults 18+
  • Seen by clinician at one of the intervention practices at least once in the prior 2 years
  • History of Hypertension (ICD Code) PLUS ≥1 of the below:
    • Outpatient BP \>150/100 on 2 or more occasions
    • Three or more current antihypertensive medication prescriptions
    • Potassium level \<3.5mEq/L or potassium supplement prescription in the last 5 years
    • History of Atrial Fibrillation or Atrial Flutter (ICD Code)

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Brigham and Women's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

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