Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05730309

Point-of-care Ultrasound and Treatment Disparities for Left Ventricular Hypertrophy

Led by Yale University · Updated on 2025-04-10

200

Participants Needed

1

Research Sites

111 weeks

Total Duration

On this page

Sponsors

Y

Yale University

Lead Sponsor

R

Robert E. Leet and Clara Guthrie Patterson Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

The objective of the proposed project is to quantify the prevalence and disparities of undiagnosed left ventricular hypertrophy (LVH) in Emergency Department (ED) patients with persistently elevated asymptomatic BP, and to measure the effect of disclosure, education, and expedited referral on 3-month outpatient follow-up and treatment rates for ED patients with newly diagnosed LVH by POCUS. Additionally, investigators will create a database of annotated clips for future development of a machine learning algorithm for LVH detection on POCUS.

CONDITIONS

Official Title

Point-of-care Ultrasound and Treatment Disparities for Left Ventricular Hypertrophy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Two blood pressure measurements greater than 140 mmHg systolic and greater than 90 mmHg diastolic on two separate vital sign checks obtained as part of routine ED care
Not Eligible

You will not qualify if you...

  • Subjects in extremis or lacking capacity to consent
  • Active treatment of hypertension within the last year
  • History of/known left ventricular hypertrophy
  • Active cardiac disease under the care of a cardiologist within last year
  • Suspicion for hypertensive emergency by treating ED physician
  • Admission to the hospital

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Yale New Haven Hospital

New Haven, Connecticut, United States, 06512

Actively Recruiting

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Research Team

C

Cristiana Baloescu, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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