Sign in

NCT06376851Active, not recruiting

AI DErived Plaque Quantification: CCTA and AI-QCPA for Determining Effective CAD Management

DECIDE Registry: AI DErived Plaque Quantification: CCTA and AI-QCPA for Determining Effective CAD Management

Source: ClinicalTrials.gov · Last updated 15 Sept 2026

Brief summary (registry, in English)

The objective of HeartFlow's DECIDE Registry is to collect observational data about the management of patients before and after HeartFlow Artificial Intelligence-Quantitative Coronary Plaque Analysis (AI-QCPA).

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
20000 (estimated)
First submitted
28 Mar 2024
Start date
27 Mar 2024
Primary completion date
27 Mar 2026
Lead sponsor
HeartFlow, Inc.
NCT number
NCT06376851

What you commit to

  • Study type: Observational
  • Planned participants: 20000
  • From 27 Mar 2024 to the primary completion date, 27 Mar 2026
  • 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.

Prior treatment

  • Groups 1,2,3,4, and 6: Previous history of CAD (prior to the CCTA or stress test with history of revascularization)
  • Group 5: Prior history of PCI in multiple vessel territories, PCI in the Left Main, CABG, and/or any other conditions or limitations which would prevent successful CCTA processing by HeartFlow
  • Previously evaluated with and/or in a study which includes AI-QCPA

Other

  • ED presentation (at the time of the CCTA or stress test)
  • Acute chest pain (in patients who have not been ruled out for ACS)

Who the study is looking for

  • Groups 1, 2,4,5 and 6: CCTA and plaque detected
  • Group 3: Any patient with a stress test (stress echocardiogram or nuclear imaging including SPECT or PET) and no CCTA within the 90 days prior to site activation
  • Groups 1,2,3 and 4: Clinically stable, symptomatic
  • Group 6: Clinically stable without symptoms suggestive of CAD at the time of the CCTA

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Moses Cone Memorial Hospital
Coordinator of this site? Confirm its status
GreensboroUnited StatesUnknown status

Related publications

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