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Clinical Trials/NCT04569669
NCT04569669
Unknown
Not Applicable

A Clinical Trial on the Diagnostic Performance Based on CT-Derived Fractional Flow Reserve Score Analysis Software for Coronary Artery Stenosis

CCRF Inc., Beijing, China8 sites in 1 country325 target enrollmentOctober 9, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Stenosis
Sponsor
CCRF Inc., Beijing, China
Enrollment
325
Locations
8
Primary Endpoint
Sensitivity and specificity (subject level) of FFRCT
Last Updated
5 years ago

Overview

Brief Summary

The device involved in this trail is a diagnostic software with a Prospective, Multicenter, Self Controlled design. FFRCT diagnostic performance was calculated by CardioSimFFRct Analysis software, and the diagnostic accuracy, sensitivity, specificity, positive predictive value and negative predictive performance of FFRCT for myocardial ischemia were calculated per-patient level and per-vessel level with invasive FFR value as gold standard.

Detailed Description

The present study is a single arm, open label, prospective trial. Measurement of FFR during invasive cardiac catheterization represents the "gold standard" for assessment of the hemodynamic significance of coronary artery lesions. As we know, the major disadvantage of FFR is that it has to be measured invasively. CardioSimFFRct Analysis software is a non-invasive method to determine FFR which computes the hemodynamic significance of Coronary Artery Disease (FFRCT) from coronary computed tomography angiography(CCTA)data of the subject by using computational fluid dynamics.The FFR derived from FFR-CT will be compared with invasive FFR as gold standard.Moreover CardioSimFFRct also simplifies the coronary artery into a one-dimensional piping model, omits grid engineering, and greatly reduces the complexity of pretreatment.Based on the pressure loss along the pipe flow and the local pressure loss, a fast method for FFR calculation in engineering is proposed. The calculation time can be reduced to several minutes. FFRct from CardioSimFFRct Analysis software is mainly based on CCTA images to image the coronary arteries. Through three-dimensional reconstruction of the coronary arteries and computational fluid Dynamics (CFD) technology, the simulation of blood flow in the blood vessels is realized to extract the coronary blood flow reserve score (FFR).FFRct has the following characteristics such as the FFR value can be measured noninvasively, without additional damage to patients, avoiding the risks brought by invasive surgery, and the side effects brought by drugs during invasive surgery.FFRct can realize the examination quickly, save the time of doctors' coronary functional assessment, and simplify the process of coronary functional assessment.It also has the function of three-dimensional reconstruction of blood vessels, which makes it convenient for users to view the whole structure of coronary arteries and make artificial correction.The results of FFRct have high repeatability and are easy for users to evaluate.

Registry
clinicaltrials.gov
Start Date
October 9, 2020
End Date
March 9, 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
CCRF Inc., Beijing, China
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects that participate in this study must fulfill all the following criteria:
  • General inclusion criteria:
  • Age ≥18 years and ≤ 80 years;
  • Subject providing written informed consent;
  • After the researcher assessed the suspected presence of coronary artery stenosis, coronary angiography and CCTA examination were proposed.
  • Angiographic inclusion criteria:
  • CCTA inspection should be performed on instruments with at least 64 multidetector rows;
  • CCTA images are clear and readable;
  • The diameter of coronary artery lesion stenosis was measured by CCTA image with 30%-90%;
  • The reference vessel diameter of coronary stenosis was ≥2.5mm by CCTA imaging.

Exclusion Criteria

  • If subjects fulfill any of below criteria, this subject shall be exclude from this study.
  • General exclusion criteria:
  • Pregnant and breast-feeding women;
  • Previous ST-segment elevation myocardial infarction 30 days before CCTA examination, and a history of non-ST-segment elevation myocardial infarction 7 days before CCTA examination;
  • Prior Coronary Artery Bypass Graft(CABG),Pacemaker, Implantable Cardioverter Defibrillator(ICD), Artificial Valve Implantation;
  • Hypertrophic obstructive cardiomyopathy;
  • Heart failure(NYHA≥III or Left Ventricular Ejection Fraction(LVEF)\< 40%);
  • Atrial fibrillation, supraventricular tachycardia, ventricular tachycardia and other arrhythmias;
  • Body mass index \>35kg/m2;
  • Serum creatinine \>178µmol/L or 2mg/dl;

Outcomes

Primary Outcomes

Sensitivity and specificity (subject level) of FFRCT

Time Frame: Measurement at Procedure/Baseline Visit

Sensitivity and specificity (subject level) for predicting the functional significance of coronary artery stenosis using CT-Derived Fractional Flow Reserve Score Analysis Software.

Secondary Outcomes

  • Positive Predictive Value (PPV) between FFRCT vs. FFR(Measurement at Procedure/Baseline Visit)
  • Sensitivity and Specificity between FFRCT vs. FFR(Measurement at Procedure/Baseline Visit)
  • Negative Predictive Value (NPV) between FFRCT vs. FFR(Measurement at Procedure/Baseline Visit)
  • AUC between FFRCT vs. FFR(Measurement at Procedure/Baseline Visit)
  • Accuracy (lesion level and subject level) between FFRCT vs. FFR(Measurement at Procedure/Baseline Visit)

Study Sites (8)

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