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

NAActive, not recruitingINTERVENTIONAL
Enrollment

12,501

Participants

Timeline

Start Date

March 13, 2024

Primary Completion Date

December 9, 2024

Study Completion Date

December 31, 2029

Conditions
Primary AldosteronismResistant HypertensionSecondary HypertensionHyperaldosteronismMineralocorticoid ExcessHypertension
Interventions
OTHER

Best Practice Advisory Computerized Alert

For patients randomly assigned to the BPA Alert Group, an on-screen electronic alert will be issued during the outpatient clinical encounter than notifies the clinician that their patient should be screened for PA. The clinician will be provided with on-screen details of which patient-specific risk factors qualified them for PA screening and with an option to order a plasma renin activity, aldosterone, and basic metabolic panel. If screening labs are ordered, the clinician will also receive an option to order an eConsult for expert guidance on interpretation of the test results. If the clinician does not order the PA screening labs, they will be able to continue with clinical EHR documentation but will need to select a reason they opted not to follow the alert's evidence-based clinical practice recommendation.

Trial Locations (1)

02115

Brigham and Women's Hospital, Boston

All Listed Sponsors
collaborator

National Heart, Lung, and Blood Institute (NHLBI)

NIH

lead

Brigham and Women's Hospital

OTHER

NCT05925569 - Electronic Alert to Improve Testing For Primary Aldosteronism in Patients With Hypertension | Biotech Hunter | Biotech Hunter