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Randomized-controlled Trial of a Combined vs. Conventional Percutaneous Intervention for Near-Infrared Spectroscopy Defined High-Risk Native Coronary Artery Lesions (CONCERTO)

Primary Purpose

Arteriosclerosis, Near-infrared Spectroscopy, Peri-procedural Myocardial Infarction

Status
Terminated
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Combined Intervention
Conventional PCI
Sponsored by
North Texas Veterans Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Arteriosclerosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥18 years.
  2. Willing and able to provide informed consent and able to comply with study procedures and follow-up.
  3. Undergoing a clinically indicated left heart coronary catheterization
  4. Need PCI of a high-risk native coronary artery lesion. High-risk lesions will be defined as lesions with ≥2 contiguous yellow blocks on block chemogram.

Exclusion Criteria:

  1. Coexisting conditions that limit life expectancy to less than 30-days or that could affect the patient's compliance with the protocol.
  2. Positive pregnancy test or breast-feeding.
  3. High risk for bleeding.
  4. Subject is currently, or within the 30 preceding days, participating in a device or pharmaceutical treatment protocol.
  5. Clinical presentation with ST-segment elevation MI.
  6. Persistent (>10 minutes) hypotension (systolic blood pressure <90 mmHg)
  7. Need for revascularization of multiple lesions during the index PCI.
  8. Unprotected left main (>50%) or equivalent left main disease.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Combined Intervention

    Conventional PCI

    Arm Description

    Combined intervention: pre-PCI intracoronary vasodilator and glycoprotein IIb/IIIa inhibitor administration, use of an EPD if technically feasible, and complete coverage of the lipid core plaque, if technically feasible

    Conventional PCI

    Outcomes

    Primary Outcome Measures

    Reduction of the incidence and size of periprocedural MI, as assessed by the peak post-PCI troponin distribution

    Secondary Outcome Measures

    Reduction in the incidence of >3x and >10x upper limit of normal increase in CK-MB
    Reduction in the incidence of slow flow/no-reflow post PCI
    Lower incidence of major adverse cardiac events, defined as the composite of death, acute coronary syndrome, or coronary revascularization) during 30-day follow-up

    Full Information

    First Posted
    November 6, 2015
    Last Updated
    June 27, 2016
    Sponsor
    North Texas Veterans Healthcare System
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02601664
    Brief Title
    Randomized-controlled Trial of a Combined vs. Conventional Percutaneous Intervention for Near-Infrared Spectroscopy Defined High-Risk Native Coronary Artery Lesions
    Acronym
    CONCERTO
    Official Title
    Randomized-controlled Trial of a Combined vs. Conventional Percutaneous Intervention for Near-Infrared Spectroscopy Defined High-Risk Native Coronary Artery Lesions
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2016
    Overall Recruitment Status
    Terminated
    Why Stopped
    Due to lack of eligible patients.
    Study Start Date
    November 2015 (undefined)
    Primary Completion Date
    January 2016 (Actual)
    Study Completion Date
    February 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    North Texas Veterans Healthcare System

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Design: Single center, single-blind randomized controlled trial of patients with high risk native coronary artery lesions (defined as ≥2 contiguous yellow blocks on the block chemogram) requiring clinically indicated percutaneous coronary intervention. Patients will be randomized to either a combined intervention or conventional PCI. Cardiac biomarker measurements will be performed before PCI and 18-24 hours later. Treatment: Combined intervention consisting of pre-PCI intracoronary vasodilator and glycoprotein IIb/IIIa inhibitor administration, use of an EPD if technically feasible, and complete coverage of the lipid core plaque, if technically feasible. Control: Conventional PCI. Duration: 30 days follow-up. The primary trial objective is to compare the incidence and size of periprocedural MI, as assessed by the peak post-PCI troponin distribution in the two study groups. The secondary endpoints are: (1) Reduction in the incidence of >3x and >10x upper limit of normal increase in CK-MB. (2) Reduction in the incidence of slow flow/no-reflow post PCI. (3) Lower incidence of major adverse cardiac events, defined as the composite of death, acute coronary syndrome, or coronary revascularization) during 30-day follow-up.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Arteriosclerosis, Near-infrared Spectroscopy, Peri-procedural Myocardial Infarction, Coronary Artery Disease

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    3 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Combined Intervention
    Arm Type
    Active Comparator
    Arm Description
    Combined intervention: pre-PCI intracoronary vasodilator and glycoprotein IIb/IIIa inhibitor administration, use of an EPD if technically feasible, and complete coverage of the lipid core plaque, if technically feasible
    Arm Title
    Conventional PCI
    Arm Type
    Active Comparator
    Arm Description
    Conventional PCI
    Intervention Type
    Procedure
    Intervention Name(s)
    Combined Intervention
    Intervention Description
    pre-PCI intracoronary vasodilator administration and glycoprotein IIb/IIIa inhibitor administration, use of an embolization protection device if technically feasible, and complete coverage of the lipid core plaque, if technically feasible
    Intervention Type
    Procedure
    Intervention Name(s)
    Conventional PCI
    Intervention Description
    Conventional PCI
    Primary Outcome Measure Information:
    Title
    Reduction of the incidence and size of periprocedural MI, as assessed by the peak post-PCI troponin distribution
    Time Frame
    18-24 hours post-procedure
    Secondary Outcome Measure Information:
    Title
    Reduction in the incidence of >3x and >10x upper limit of normal increase in CK-MB
    Time Frame
    18-24 hours post-procedure
    Title
    Reduction in the incidence of slow flow/no-reflow post PCI
    Time Frame
    2-3 hours after
    Title
    Lower incidence of major adverse cardiac events, defined as the composite of death, acute coronary syndrome, or coronary revascularization) during 30-day follow-up
    Time Frame
    30 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age ≥18 years. Willing and able to provide informed consent and able to comply with study procedures and follow-up. Undergoing a clinically indicated left heart coronary catheterization Need PCI of a high-risk native coronary artery lesion. High-risk lesions will be defined as lesions with ≥2 contiguous yellow blocks on block chemogram. Exclusion Criteria: Coexisting conditions that limit life expectancy to less than 30-days or that could affect the patient's compliance with the protocol. Positive pregnancy test or breast-feeding. High risk for bleeding. Subject is currently, or within the 30 preceding days, participating in a device or pharmaceutical treatment protocol. Clinical presentation with ST-segment elevation MI. Persistent (>10 minutes) hypotension (systolic blood pressure <90 mmHg) Need for revascularization of multiple lesions during the index PCI. Unprotected left main (>50%) or equivalent left main disease.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Emmanouil S Brilakis, MD, PhD
    Organizational Affiliation
    North Texas Veterans Healthcare System
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    22511587
    Citation
    Brilakis ES, Abdel-Karim AR, Papayannis AC, Michael TT, Rangan BV, Johnson JL, Banerjee S. Embolic protection device utilization during stenting of native coronary artery lesions with large lipid core plaques as detected by near-infrared spectroscopy. Catheter Cardiovasc Interv. 2012 Dec 1;80(7):1157-62. doi: 10.1002/ccd.23507. Epub 2012 Apr 17.
    Results Reference
    background
    PubMed Identifier
    21575750
    Citation
    Raghunathan D, Abdel-Karim AR, Papayannis AC, daSilva M, Jeroudi OM, Rangan BV, Banerjee S, Brilakis ES. Relation between the presence and extent of coronary lipid core plaques detected by near-infrared spectroscopy with postpercutaneous coronary intervention myocardial infarction. Am J Cardiol. 2011 Jun 1;107(11):1613-8. doi: 10.1016/j.amjcard.2011.01.044.
    Results Reference
    background
    PubMed Identifier
    24254480
    Citation
    Patel VG, Brayton KM, Mintz GS, Maehara A, Banerjee S, Brilakis ES. Intracoronary and noninvasive imaging for prediction of distal embolization and periprocedural myocardial infarction during native coronary artery percutaneous intervention. Circ Cardiovasc Imaging. 2013 Nov;6(6):1102-14. doi: 10.1161/CIRCIMAGING.113.000448. No abstract available.
    Results Reference
    background
    PubMed Identifier
    26003018
    Citation
    Stone GW, Maehara A, Muller JE, Rizik DG, Shunk KA, Ben-Yehuda O, Genereux P, Dressler O, Parvataneni R, Madden S, Shah P, Brilakis ES, Kini AS; CANARY Investigators. Plaque Characterization to Inform the Prediction and Prevention of Periprocedural Myocardial Infarction During Percutaneous Coronary Intervention: The CANARY Trial (Coronary Assessment by Near-infrared of Atherosclerotic Rupture-prone Yellow). JACC Cardiovasc Interv. 2015 Jun;8(7):927-36. doi: 10.1016/j.jcin.2015.01.032. Epub 2015 May 20.
    Results Reference
    background
    PubMed Identifier
    25266075
    Citation
    Erlinge D, Harnek J, Goncalves I, Gotberg M, Muller JE, Madder RD. Coronary liposuction during percutaneous coronary intervention: evidence by near-infrared spectroscopy that aspiration reduces culprit lesion lipid content prior to stent placement. Eur Heart J Cardiovasc Imaging. 2015 Mar;16(3):316-24. doi: 10.1093/ehjci/jeu180. Epub 2014 Sep 28.
    Results Reference
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