FORECAST: Fluid-dynamics in Bifurcation PCI

Sponsor
Catholic University of the Sacred Heart (Other)
Overall Status
Unknown status
CT.gov ID
NCT03174418
Collaborator
(none)
300
1
42
7.2

Study Details

Study Description

Brief Summary

Investigator-initiated, international, multicentre, observational study with two cohorts.

The two study cohorts will be:

Cohort A: to understand if the local blood flow patterns (associated with low WSS), as evaluated by computational fluid dynamic tools from combined angiographic and OCT invasive images, may better predict the clinical outcome of patients with bifurcated coronary lesions treated by PCI.

Cohort B: to understand if the local blood flow patterns (associated with low WSS), as evaluated by computational fluid dynamic tools from combined angiographic and OCT invasive images, may better predict the clinical outcome of patients with sub-critical bifurcated lesions managed conservatively.

Coronary angiography and OCT images will be combined to obtain a three-dimensional model of the diseased coronary vessels that will be used to calculate the local blood flow patterns and the time-averaged WSS at the bifurcated lesion level by using computational fluid dynamics software.

Baseline (in patients both managed conservatively and treated by PCI) and post-PCI (in patients treated by PCI) images will be processed.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Coronary angiography and optical coherence tomography

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Multicentre Prospective Study on the Role of Fluid Dynamics OCT-based REconstruction of Coronary Atherosclerosis in bifurcationS to Predict ouTcome
Anticipated Study Start Date :
Sep 1, 2017
Anticipated Primary Completion Date :
Sep 1, 2018
Anticipated Study Completion Date :
Mar 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Cohort A

Patients with bifurcated coronary lesions treated by percutaneous coronary interventions.

Procedure: Coronary angiography and optical coherence tomography
Coronary angiography and OCT images will be combined to obtain a three-dimensional model of the diseased coronary vessels that will be used to calculate the local blood flow patterns and the arterial time-averaged wall shear stress at the bifurcated lesion level

Cohort B

Patients with untreated bifurcated coronary lesions.

Procedure: Coronary angiography and optical coherence tomography
Coronary angiography and OCT images will be combined to obtain a three-dimensional model of the diseased coronary vessels that will be used to calculate the local blood flow patterns and the arterial time-averaged wall shear stress at the bifurcated lesion level

Outcome Measures

Primary Outcome Measures

  1. Target bifurcation failure (TBF) [1,6,12,18,24 and 36 months]

    - Target bifurcated lesion-related major adverse coronary event (MACE) defined as the composite of: cardiac death myocardial infarction (MI) not clearly related with another vessel target vessel revascularization (TVR)

Secondary Outcome Measures

  1. Target vessel failure [1,6,12,18,24 and 36 months]

    - In the absence of target bifurcated lesion-related MACE, target bifurcated lesion angiographic failure defined, in patients treated by PCI, as: > 50% restenosis on the main vessel (MV) or TIMI (Thrombolysis In Myocardial Infarction) flow < 3 on the side branch (SB) at angiography eventually performed during the clinical course.

  2. Bifurcated lesion angiographic failure [1,6,12,18,24 and 36 months]

    Cardiac death MI TVR Definite or probable stent thrombosis

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

  • Patients with stable or unstable coronary artery disease;

  • TIMI 3 on both MV and SB;

  • MV visual diameter > 2.5 mm;

  • SB visual diameter > 2.0 mm;

  • Documentation of angiographically-critical (visually estimated percentage diameter stenosis ≥80% <100%) coronary lesion treated by PCI and underwent post-PCI OCT assessment or angiographically-intermediate (visually estimated percentage diameter stenosis ranging between 30-80%) lesion in the MV considered suitable for conservative management (myocardial revascularization not planned).

Exclusion Criteria

  • Age < 18 years or impossibility to give informed consent.

  • Female sex with child-bearing potential.

  • Life expectancy of less than 12 months or factors making clinical follow-up difficult (no fixed address, etc.).

  • Ascertained or suspected contraindications to prolonged (up to 6 month) double antiplatelet therapy.

  • Known hypersensitivity to aspirin, heparin, contrast dye, sirolimus, everolimus, zotarolimus, cobalt, chromium, nickel, tungsten acrylic, and fluoro-polymers.

  • Poor cardiac function as defined by left ventricular global ejection fraction ≤ 30%.

  • Recent (< 48 hours) ST-segment elevation myocardial infarction.

  • Severe myocardial hypertrophy (interventricular septum thickness > 15 mm, ECG Sokolow's criteria fulfilled).

  • Severe valvular heart disease.

  • Significant platelet count alteration (<100,000 cells/mm3 or > 700,000 cells/mm3).

  • Gastrointestinal bleeding requiring surgery or blood transfusions within 4 previous weeks.

  • History of clotting pathology.

  • Advance renal failure with glomerular filtration rate < 30 ml/min (Cockcroft-Gault equation)

  • Left main lesion.

  • Target bifurcation located on a distal coronary segment.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Policlinico A. Gemelli. Università Cattolica del Sacro Cuore Roma Italy 00168

Sponsors and Collaborators

  • Catholic University of the Sacred Heart

Investigators

  • Principal Investigator: Francesco Burzotta, MD, Policlinico A. Gemelli. Università Cattolica del Sacro Cuore

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Francesco Burzotta, MD, PhD, Catholic University of the Sacred Heart
ClinicalTrials.gov Identifier:
NCT03174418
Other Study ID Numbers:
  • 01012017
First Posted:
Jun 2, 2017
Last Update Posted:
Jun 2, 2017
Last Verified:
May 1, 2017
Keywords provided by Francesco Burzotta, MD, PhD, Catholic University of the Sacred Heart
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 2, 2017