The PRECISE Protocol: Prospective Randomized Trial of the Optimal Evaluation of Cardiac Symptoms and Revascularization

NACompletedINTERVENTIONAL
Enrollment

2,103

Participants

Timeline

Start Date

November 27, 2018

Primary Completion Date

May 20, 2022

Study Completion Date

May 20, 2022

Conditions
Coronary Artery Disease
Interventions
DIAGNOSTIC_TEST

cCTA with selective FFRct

PRECISE will evaluate whether a precision evaluation strategy that combines contemporary risk stratification using the PROMISE Risk Tool with functional and anatomic non-invasive evaluation with cCTA with selective FFRct can improve outcomes over usual care in stable chest pain patients while safely deferring further testing in low-risk patients and reducing cost overall

Trial Locations (1)

70601

Participating site, Lake Charles

Sponsors
All Listed Sponsors
collaborator

Duke Clinical Research Institute

OTHER

collaborator

Cardiovascular Research Foundation, New York

OTHER

lead

HeartFlow, Inc.

INDUSTRY