CClinicalTrials.gg
Enrolling by invitationNCT06749132Updated May 8, 2026

Deep Learning-enhanced Personalized Monitoring of Aortic Stenosis - The DETECT-AS Prognostic Study

An observational study in Aortic Stenosis, sponsored by Yale University. Enrolling by invitation at 3 sites in United States. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2026-05-08.

Sponsored by Yale University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
210
Ages
65 Years and older
Sex
All
01

Study summary

This study will evaluate the validity of a digital biomarker score for precision risk stratification among older adults with aortic sclerosis or mild aortic stenosis (AS) at three US health systems.

02

Conditions studied

  • Aortic Stenosis

Browse trials for

Keywords

  • aortic stenosis
  • artificial intelligence
03

In context

Aortic Valve Stenosis

985 studies on the registry are indexed under Aortic Valve Stenosis; 283 are open to participants now.

This study's planned enrollment of 210 is close to the median of 200 across 424 observational studies indexed under Aortic Valve Stenosis.

Browse Aortic Valve Stenosis studies →

Lead sponsor

Yale University is the lead sponsor of 1,725 studies on the registry; 299 are open to participants now.

Of its 210 completed or terminated interventional studies of FDA-regulated products, 126 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

US adults aged 65 and older with an echocardiogram within the prior 2-3 years that showed aortic sclerosis without stenosis or mild aortic stenosis (AS).

Inclusion criteria

  1. Age 65 years or older
  2. Prior transthoracic echocardiogram within the past 2-3 years showing aortic sclerosis without stenosis or mild AS

Exclusion criteria

Exclusion Criteria:

  1. Opted out of research studies
  2. Non-English speaking
  3. Any echocardiogram within 24 months of medical record review.
  4. Prior history of aortic valve replacement or repair, including transcatheter and surgical AVR with either a bioprosthetic or mechanical valve
  5. Presence of implantable cardiac devices, including permanent cardiac pacer, implantable cardioverter-defibrillator, or left ventricular assist device
  6. Prior heart transplant
  7. History of dementia
  8. Unable to attend study visit at echocardiogram lab within four years of most recent echocardiogram.
  9. Documented life expectancy of \<1 year or current participation in hospice services
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
210 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testTransthoracic echocardiogram

    All study participants will undergo a clinical transthoracic echocardiogram (TTE) performed by certified echocardiography technicians. The TTE includes standard transthoracic examination with acquisition of B-mode, color and spectral Doppler images and videos in line with standard echocardiographic guidelines.

06

What researchers measure

Primary outcomes

  1. Annualized change in AV Vmax in m/sec/years

    The primary outcome measure is the annualized change in AV Vmax in m/sec/years, defined as the absolute difference between the value on the enrollment and baseline echocardiogram measurement, divided by the time difference between the studies.

    Time frame: From baseline TTE to TTE performed at enrollment

07

Study locations

3 sites
  • Yale New Haven Health System
    New Haven, Connecticut 06519, United States
  • Icahn School of Medicine at Mount Sinai
    New York, New York 10029, United States
  • The Methodist Hospital Research Institute
    Houston, Texas 77030, United States
08

References and documents

Individual participant data

Plan to share: Yes — A de-identified dataset will be made available following publication of primary results.

Supporting information: Study protocol, Sap, Icf, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06749132
Lead sponsor
Yale University
Collaborators
National Institute on Aging (NIA), Icahn School of Medicine at Mount Sinai, The Methodist Hospital Research Institute
Responsible party
Sponsor
First posted
Dec 27, 2024
Start date
May 6, 2026
Primary completion
Aug 31, 2028 (estimated)
Completion
Aug 31, 2028 (estimated)
Last update
May 8, 2026

Study contacts

Rohan Khera, MD, MS
principal investigator · Yale University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion