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
About this trial
This is an interventional treatment trial for Arteriosclerosis
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.
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
NCT ID
NCT02601664
First Posted
November 6, 2015
Last Updated
June 27, 2016
Sponsor
North Texas Veterans Healthcare System
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
background
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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
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