FFRB: Validation of a Predictive Model of Coronary Fractional Flow Reserve in Patients With Intermediate Coronary Stenosis

Sponsor
National Heart Centre Singapore (Other)
Overall Status
Unknown status
CT.gov ID
NCT03054324
Collaborator
(none)
132
2
27.9
66
2.4

Study Details

Study Description

Brief Summary

Coronary fraction flow reserve (FFR), the ratio of the mean coronary pressure distal to a coronary stenosis to the mean aortic pressure during maximal coronary blood flow (hyperemia), defines the hemodynamic significance of coronary artery narrowing. Noninvasive assessment of FFR via a combination of computational fluid dynamics (CFD) and coronary CT angiography CCTA (the so-called FFRCT) has potential. Coronary computed tomographic angiography is a noninvasive test for diagnosis of anatomic coronary stenosis (i.e., narrowing of a blood vessel). A new analytical model of FFR from the general Bernoulli equation (conservation of energy) (FFRB) is simple and has potential. A collaborator group has recently developed a new analytical model to quantify pressure drop, and hence FFR, based on lesion dimensions (i.e., the cross-section area along the lesion and the length of lesion) and coronary flow, with no empirical parameters. The investigators hypothesize that this new model will allow quantification of FFR (FFRB) in a cohort of human patients with intermediate coronary stenosis. The study will compare FFRB with invasive FFR measurements from invasive coronary angiography (ICAG).

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Fractional Flow Reserve

Detailed Description

Coronary fraction flow reserve (FFR), the ratio of the mean coronary pressure distal to a coronary stenosis to the mean aortic pressure during maximal coronary blood flow (hyperemia), defines the hemodynamic significance of coronary artery narrowing. Recent landmark studies showed a clear benefit of FFR in guiding percutaneous coronary intervention (PCI) for better clinical outcome and cost-effectiveness. The reference method for FFR measurement requires the use of a pressure wire inserted across the stenosis invasively. Therefore, a non-invasive method to quantify FFR is clinically desired.

Noninvasive assessment of FFR via a combination of computational fluid dynamics (CFD) and coronary CT angiography CCTA (the so-called FFRCT) has potential. Coronary computed tomographic angiography is a noninvasive test for diagnosis of anatomic coronary stenosis (i.e., narrowing of a blood vessel). However, CCTA alone does not determine whether a stenosis causes ischemia. Computational fluid dynamics (CFD), applied to CCTA images, enables computation of FFR (FFRCT). Recent studies have demonstrated the potential of FFRCT as a promising noninvasive method for identification of individual lesion with ischemia from both single centre and multi-centre prospective studies. However, the FFRCT is currently performed remotely and it takes several hours to complete the computation for each study. This potentially impedes the wider clinical application of FFRCT.

A new analytical model of FFR from the general Bernoulli equation (conservation of energy) (FFRB) is simple and has potential. The Bernoulli equation has many clinical applications. A collaborator group has recently developed a new analytical model to quantify pressure drop, and hence FFR, based on lesion dimensions (i.e., the cross-section area along the lesion and the length of lesion) and coronary flow, with no empirical parameters. The investigators validated it using in vitro and in vivo experiments and finite-element method. The study team hypothesize that this new model will allow quantification of FFR (FFRB) in a cohort of human patients with intermediate coronary stenosis. The investigators will compare FFRB with invasive FFR measurements from invasive coronary angiography (ICAG).

Aims and Objectives

Primary aim: Diagnostic performance of FFRB with CCTA data in patients with intermediate coronary artery disease (CAD), as compared to an invasive FFR reference standard (FFR<=0.80)

Secondary aims: Diagnostic performance with FFRB for lesions of intermediate stenosis severity; Determining the per-vessel correlation of FFRB value to FFR from ICA

Study Design

Study Type:
Observational
Anticipated Enrollment :
132 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
FFRB Study: Validation of a Predictive Model of Coronary Fractional Flow Reserve in Patients With Intermediate Coronary Stenosis
Actual Study Start Date :
Sep 2, 2016
Anticipated Primary Completion Date :
Dec 31, 2018
Anticipated Study Completion Date :
Dec 31, 2018

Outcome Measures

Primary Outcome Measures

  1. Diagnostic performance of FFRB to invasive FFR [6 months from CT Angiogram]

    The diagnostic performance of FFRB with CCTA data in patients with intermediate coronary artery disease (CAD), as compared to an invasive FFR reference standard (FFR<=0.80)

Secondary Outcome Measures

  1. Diagnostic performance with FFRB for lesions of intermediate stenosis severity [6 months from CT Angiogram]

  2. Per-vessel correlation of FFRB to invasive FFR [6 months from CT Angiogram]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 98 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 21-98.

  • Underwent CCTA within 180 days and is scheduled to undergo coronary angiography and FFR in vessels having diameter stenosis between 30-90%, and deemed clinically indicated for evaluation.

Exclusion Criteria:
  • Previous PCI

  • Previous coronary artery bypass surgery

  • Contraindication to beta blockers , nitroglycerin or adenosine, including second- or third-degree heart block; sick sinus syndrome; long QT syndrome; severe hypotension; asthma, chronic obstructive pulmonary disease, heart rate <50 beats/min.

  • Acute coronary syndrome (acute myocardial infarction, unstable angina or unstable arrhythmias) is suspected.

  • Had recent myocardial infarction within 30 days before CCTA or between CCTA and coronary angiography

  • Has known complex congenital heart disease.

  • Has had pacemaker or internal defibrillator leads implanted.

  • Has a prosthetic heart valve or significant valvular pathology.

  • Has tachycardia or significant arrhythmia; heart rate ≥ 100 beats/min; systolic blood pressure ≤90 mmHg.

  • Renal dysfunction (glomerular filtration rate (GFR) <30 mL/min/1.73m2).

  • Allergy to iodinated contrast.

  • Individuals unable to provide informed consent.

  • Non-cardiac illness with life expectancy <2 years.

  • Pregnant state.

  • Canadian Cardiovascular Society class IV angina.

  • Patients with a left ventricular ejection fraction less than 30%.

  • Patients with hypertrophic cardiomyopathy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 National University Hospital Singapore Singapore 119074
2 National Heart Centre Singapore Singapore Singapore 169609

Sponsors and Collaborators

  • National Heart Centre Singapore

Investigators

  • Principal Investigator: Soo Teik Lim, MBBS, National Heart Centre Singapore

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Heart Centre Singapore
ClinicalTrials.gov Identifier:
NCT03054324
Other Study ID Numbers:
  • 2016/2097
First Posted:
Feb 15, 2017
Last Update Posted:
Oct 18, 2018
Last Verified:
Mar 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Heart Centre Singapore
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 18, 2018