Functional Diagnostic Accuracy of Quantitative Flow Ratio in Tandem Lesions and Virtual Stenting

• Conditions: Heart Diseases; Vascular Diseases; Coronary Artery Disease; Cardiovascular Diseases; Arteriosclerosis; Myocardial Ischemia; Arterial Occlusive Diseases

• Registration Number: NCT03405506
• Lead Sponsor: Pulse Medical Imaging Technology (Shanghai) Co., Ltd

Brief Summary

Quantitative Flow Ratio (QFR) is a novel method for evaluating the functional significance of coronary stenosis. Virtual stent implantation technique combined with QFR was recently developed to predict the functional significance of coronary stenosis as if the stenosis was revascularized.

The purpose of this study is to evaluate the diagnostic accuracy of QFR in in tandem lesions with fractional flow reserve (FFR) as the reference standard. The secondary purpose is to evaluate the diagnostic accuracy of QFR-based virtual stent technique in predicting the FFR values after revascularizing the culprit lesion.

Detailed Description

QFR is a novel method for evaluating the functional significance of coronary stenosis by calculation of the pressure drop in the vessel. 3D coronary models can be reconstructed based on two angiographic projections to obtain the geometric parameters, including vascular diameter or cross-sectional area. According to the lesion stenosis, vessel curvature, conical geometry and reference lumen characteristics, pressure drop can be calculated in real time based on its relationship with blood flow. There is no need for pressure wire and adenosine / ATP induced maximum hyperemia compared with FFR.

The FAVOR Pilot Study and FAVOR II China Study showed promising results for diagnostic accuracy in consecutive patients. However, the diagnostic accuracy of QFR in specific tandem lesions needs further investigation. Furthermore, using the virtual stent technology to accurately assess the culprit lesion and choose the optimal treatment is significant in precisely guiding PCI surgery.

Study Timeline

• Status Verified: 2018-01
• Study First Submitted: 2018-01-12
• Study First Submitted QC: 2018-01-19
• Last Update Submitted: 2018-01-19
• Study First Posted: 2018-01-23
• Last Update Posted: 2018-01-23
• Study Start: 2018-02-02
• Primary Completion: 2019-02-02
• Study Completion: 2019-02-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 69

Inclusion Criteria

• General inclusion Criteria:

  1. Stable and unstable angina pectoris or secondary evaluation of stenosis after acute MI;
  2. Age > 18 years;
  3. Able to provide signed informed consent.

• Angiographic inclusion criteria:

  1. At least two localized lesions on the same coronary artery;
  2. More than 50% diameter stenosis (DS) estimated by QCA on each lesion;
  3. At least 10 mm relatively normal lumen (at most 20% DS) between two lesions;
  4. Reference vessel size > 2 mm in stenotic segment by visual estimate.

Exclusion Criteria

• General exclusion criteria:

  1. Ineligible for diagnostic intervention or FFR examination;

  2. Myocardial infarction within 72 hours;

  3. Severe heart failure (NYHA≥III);

  4. S-creatinine>150µmol/L or GFR<45 ml/kg/1.73m2;

  5. Allergy to contrast agent or adenosine;

  6. Factors that might substantially impact the angiographic image quality, e.g, frequent atrial premature beat or atrial fibrillation;

  7. Serious complications:

     1. Evidence of cardiac rupture;
     2. History of bleeding (intracranial hemorrhage, gastrointestinal bleeding, etc.);
     3. Acute or chronic blood system diseases, including hemoglobin < 10 g / L, or platelet count < 50 × 109 / L;
     4. Accompanied by other diseases might inducing life expectancy shorter than several months;
     5. History of severe renal insufficiency and hypohepatia (liver failure, cirrhosis, portal hypertension and active hepatitis)
     6. Aneurysm, arterial / venous malformation, aortic dissection;

  8. Cardiogenic shock or circulation capacity failure;

  9. Two-degree and more severe atrioventricular block, with no permanent pacemaker implanted;

  10. Pregnancy or lactation;

  11. The investigators believe that the treatment regimen may be detrimental to the patient or the enrollment of this subject may affect the specific assessment of the trial;

• Angiographic exclusion criteria:

  1. The interrogated stenosis is caused by myocardial bridge;
  2. Ostial lesions less than 3 mm to the aorta;
  3. Side branches of the bifurcation lesions with Median Classification of 111 or 101;
  4. Severe overlap or shorten of stenosis segment;
  5. Severe tortuosity of target vessel;
  6. Poor angiographic image quality precluding contour detection.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Diagnostic accuracy of QFR in tandem lesions as compared with FFR prior to intervention	1 hour	Diagnostic accuracy was defined as the concordance ratio of QFR evaluated outcomes (≤ 0.8 or \> 0.8) with the reference standard FFR evaluated outcomes (≤ 0.8 or \> 0.8)

Secondary Outcome Measures

Name	Time	Method
Diagnostic accuracy of QFR-based virtual stenting in predicting FFR values after revascularizing the culprit lesion	1 hour	Diagnostic accuracy was defined as the concordance ratio of QFR evaluated outcomes (≤ 0.8 or \> 0.8) with the reference standard FFR evaluated outcomes (≤ 0.8 or \> 0.8)

Trial Locations

Locations (1)

Shanghai Chest Hospital; 🇨🇳 Shanghai, Shanghai, China