Impact of Stress CT Myocardial Perfusion on Downstream Resources and Prognosis

NCT03976921 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2000

Last updated 2026-06-03

No results posted yet for this study

Summary

CT myocardial perfusion imaging (CTP) represents one of the newly developed CT-based techniques but its cost-effectiveness in the clinical pathway is undefined. The aim of the study is to evaluate the usefulness of combined evaluation of coronary anatomy and myocardial perfusion in intermediate to high-risk patients for suspected CAD or with known disease in terms of clinical decision-making, resource utilization and outcomes in a broad variety of geographic areas and patient subgroups.

Conditions

Interventions

DIAGNOSTIC_TEST

Integration of CCTA with stress CTP when indicated

When judged indicated, functional assessment with stress CTP perfusion will be performed on top of CCTA.

DIAGNOSTIC_TEST

Standard of care approach

(a) functional non-invasive tests (stress ECG, or imaging-based tests such as Stress Echo, Stress CMR, SPECT or PET) as a gatekeeper for ICA; (b) direct referral to ICA.

Sponsors & Collaborators

  • Semmelweis University Heart and Vascular Center

    collaborator OTHER
  • Emory University

    collaborator OTHER
  • Johns Hopkins University

    collaborator OTHER
  • Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

    collaborator OTHER
  • Vall d'Hebron Institute Research

    collaborator OTHER
  • Humanitas Research Hospital IRCCS, Rozzano-Milan

    collaborator OTHER
  • Ospedale Polispecialistico Humanitas Gavazzeni, Bergamo

    collaborator UNKNOWN
  • IRCCS San Raffaele

    collaborator OTHER
  • Mayo Clinic

    collaborator OTHER
  • Istituto Auxologico Italiano - IRCCS - Ospedale San Luca - Milano

    collaborator UNKNOWN
  • A.O.U. Città della Salute e della Scienza - Molinette Hospital

    collaborator OTHER
  • Centro Cardiologico Monzino

    lead OTHER

Principal Investigators

  • Gianluca Pontone, MD, PhD · Centro Cardiologico Monzino, IRCCS

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-01
Primary Completion
2026-06-30
Completion
2027-06-30

Countries

  • Italy

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03976921 on ClinicalTrials.gov