WE REMAIN EBC: Registry on Left Main Coronary Artery Bifurcation Percutaneous Intervention

Sponsor
G. d'Annunzio University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04321473
Collaborator
Azienda Sanitaria Locale n. 2 - Lanciano Vasto Chieti (Other), Hospital Clínico Universitario de Valladolid (Other), VZW Cardiovascular Research Center Aalst (Other), Federico II University (Other), Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other), Clinica Mediterranea (Other), Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland (Other), San Raffaele University Hospital, Italy (Other), Instituto Dante Pazzanese de Cardiologia (Other), University Medical Centre Maribor (Other), Clinica Di Montevergine (Other), Clinical Hospital Centre Zagreb (Other), Clinical Centre of Serbia (Other), Chiba University (Other), Université Paris-Sud (Other), Hospital Universitario Reina Sofia de Cordoba (Other), Mount Sinai Hospital, New York (Other), Hospital Pablo Tobón Uribe (Other), Pauls Stradins Clinical University Hospital (Other), University Hospital Monastir, Tunis (Other)
1,500
12.9

Study Details

Study Description

Brief Summary

The slowly accruing evidence on the treatment of patients with left main coronary artery (LMCA) disease drove evolution in guidelines, that currently establish equivalent safety and efficacy for percutaneous coronary intervention (PCI) as compared to surgery, with a class of recommendation that is subjected to the extension and complexity of concomitant coronary artery disease, as assessed by the SYNTAX score.

The severity of LMCA disease, although extremely relevant due to the extent of the supplied myocardium, is often difficult to assess with traditional angiography, due to lack of appropriate angiographic views, absence of a true "reference" segment, interaction with the intubating catheter. Intravascular techniques with either imaging or functional assessment have been variously tested, although with a disturbing rate of discordant results; moreover, they are frequently underused for a number of reasons, including the additional time needed to assess both left anterior descending (LAD) and left circumflex (LCx) arteries, technical challenges, costs and the small risk associated with maneuvering such devices. Fractional flow reserve (FFR) measured from the coronary angiogram (FFRangio) alone recently documented a high diagnostic accuracy compared with pressure-wire derived FFR.

As for the anatomical localization, the majority of LMCA lesions occur at the bifurcation, where PCI results are less favourable. The distal LMCA differs from the other bifurcations in several characteristics: a) a notable mismatch between the LMCA and the left anterior descending (LAD) artery, hampering the selection of an adequately sized stent, b) the presence of a trifurcation, with a large ramus arising from LMCA in about 10% of cases, c) the presence of left or co-dominant circulation, with the LMCA supplying all or nearly all left ventricular myocardium in about 15% of cases.

Therefore, although the European Bifurcation Club (EBC) recommends a provisional side branch approach in most cases of distal LMCA disease, the threshold for placing a second stent in the side branch may be lower in lesions located on LM bifurcation compared with non-LMCA bifurcations. As for double stenting, the evidence is controversial and a consensus is lacking. Moreover, the optimal treatment of patients with LM trifurcations is still undefined.

The aim of this study is therefore to determine the optimal strategy for the treatment of LM bifurcated lesions.

Condition or Disease Intervention/Treatment Phase
  • Procedure: PCI on left main

Detailed Description

PCI access site and technique will be left at the operator's discretion, as well as antithrombotic management.

No limitation will be applied for the technique of PCI. As regards data collection and endpoints, Case Report Form (CRF) will be entered on a web-based platform, where study participants will be able to access and retrieve data at any time during study progress.

In-hospital outcomes will be recorded; all patients discharged alive will be followed up with a 30-day, 6-month, and 1-year telephone interview.

On a center-to-center voluntary basis, pre-PCI and post-PCI angiographic images (made blind regarding patients' identity) will be sent to a study angiographic core-lab for Quantitative Angiography Substudy. The images will be processed using a validated quantitative coronary angiography (QCA) Bifurcation software to assess quantitative data describing bifurcation geometry before and after LMCA PCI. In the Quantitative Angiography Substudy, on exploratory bases, FFRangio data reconstructed by angiographic software will be tested against stenosis LMCA lesion severity and LMCA PCI result.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
1500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Web-based Registry on Left Main From the Euro Bifurcation Club (WE REMAIN EBC)
Anticipated Study Start Date :
Sep 1, 2020
Anticipated Primary Completion Date :
Apr 30, 2021
Anticipated Study Completion Date :
Sep 30, 2021

Outcome Measures

Primary Outcome Measures

  1. Major adverse cardiac events (MACE) [12 months]

    The composite of: death from any cause, myocardial infarction (MI), stent thrombosis (ST), defined as definite, probable or possible following the Academic Research Consortium.

Secondary Outcome Measures

  1. Death [12 months]

    All-cause death and cardiovascular death

  2. MI [12 months]

    Myocardial Infarction

  3. ST [12 months]

    Stent thrombosis (definite, probable or possible)

  4. In-hospital MACE [12 Months]

    Composite of death, MI and ST

  5. Target Vessel Revascularization (TVR) [12 Months]

    Target Vessel Revascularization

  6. Bleeding [12 Months]

    The occurrence of major bleeding, as a bleeding defined by the academic research consortium (BARC)- classified as type 3 (a, b or c) or 5 bleeding event

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients ≥18 years of age with a diagnosis of documented silent ischemia, stable angina, or acute coronary syndrome (ACS).

  • PCI with single or multiple drug-eluting stent (DES) for the treatment of lesion located at LMCA bifurcation and defined as a diameter stenosis of ≥50% by visual estimation.

Exclusion Criteria:
  • Patients who cannot give informed consent or have a life expectancy of ≤12 months;

  • Pregnant or nursing mothers. Women of child-bearing age will be asked if they are pregnant or think that they may be pregnant.

  • Contraindication or suspected intolerance to anticoagulant (heparin, bivalirudin) or oral antiplatelet therapy (aspirin, clopidogrel, prasugrel, ticagrelor).

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • G. d'Annunzio University
  • Azienda Sanitaria Locale n. 2 - Lanciano Vasto Chieti
  • Hospital Clínico Universitario de Valladolid
  • VZW Cardiovascular Research Center Aalst
  • Federico II University
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS
  • Clinica Mediterranea
  • Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland
  • San Raffaele University Hospital, Italy
  • Instituto Dante Pazzanese de Cardiologia
  • University Medical Centre Maribor
  • Clinica Di Montevergine
  • Clinical Hospital Centre Zagreb
  • Clinical Centre of Serbia
  • Chiba University
  • Université Paris-Sud
  • Hospital Universitario Reina Sofia de Cordoba
  • Mount Sinai Hospital, New York
  • Hospital Pablo Tobón Uribe
  • Pauls Stradins Clinical University Hospital
  • University Hospital Monastir, Tunis

Investigators

  • Principal Investigator: Marco Zimarino, MD, PhD, Azienda Sanitaria Locale n. 2 - Lanciano Vasto Chieti

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Marco Zimarino, MD, PhD, G. d'Annunzio University
ClinicalTrials.gov Identifier:
NCT04321473
Other Study ID Numbers:
  • WE_REMAIN_EBC_19
First Posted:
Mar 25, 2020
Last Update Posted:
Mar 27, 2020
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2020