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Clinical trialNCT06099665CompletedInterventional

Addressing Under-treatment and Health Equity in AS and MR Using an Integrated EHR Platform

SponsorTempus AIEnrollment2,118Aortic Valve StenosisMitral Regurgitation
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This multi-center, prospective, cluster-randomized controlled trial will evaluate Tempus Next automated notifications as an intervention to support identification and evaluation of patients possibly indicated for Valve Intervention (VI). This study will evaluate the impact of Tempus Next's automated notifications on: (1) Transcatheter or surgical procedure for AS or MR; and (2) Clinic visit with at least one member of the Multidisciplinary Heart Team (including time to evaluation) for patients with definitive or possible severe AS or MR on echocardiogram. These endpoints will also be examined within and between assigned groups according to race, ethnicity, sex, and geography. The primary question that will be answered: Do automated alerts sent to clinical providers decrease under-treatment of severe aortic stenosis and severe mitral regurgitation? The study will compare the rate of clinical follow-up and aortic valve surgery in a control group (no alerts sent) to a treatment group (alerts sent to an appropriate care provider).

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Wayne Batchelor, MD

    Director of Interventional Cardiology Inova Heart and Vascular Institute

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

6 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Saint Luke'S Health System

    Kansas City, Missouri, United States

  • Ohiohealth

    Columbus, Ohio, United States

  • Bon Secours Mercy Health - Lima Market

    Lima, Ohio, United States

  • Oregon Health and Science University

    Portland, Oregon, United States

  • Vanderbilt

    Nashville, Tennessee, United States

  • Bon Secours Mercy Health - Richmond Market

    Richmond, Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
27 Aug 2024
Primary completion
1 Dec 2025
Completion
1 Dec 2025
Last update posted
6 Mar 2026
Registered enrollment
2,118
Registry id
NCT06099665

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.