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Correlation Study of Imaging Data Acquired During CABG With Data Acquired in the Cath Lab (PERSEUS)

Primary Purpose

Coronary Artery Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ComboMap XT Guidewire
'SPY' NIRF During CABG
Sponsored by
East Carolina University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Coronary Artery Disease focused on measuring Fractional Flow Reserve (FFR), Instantaneous Wave Free Ratio (iFR), Coronary Flow Reserve (CFR), Hyperemic Stenosis Resistance Index (HSR), Hyperemic microvascular resistance (HMR), Wave intensity analysis (WIA), Myocardial Perfusion, SPY NIRF Regional Myocardial Perfusion Analysis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >18<80
  • Patients with stable angina or NSTEMI with total CK rise of <1000 U/litre who after planned coronary angiography are going to be referred for CABG and have at least one vessel with a visual 40-80% stenosis that is interrogated with intracoronary physiology

Exclusion Criteria:

  • Emergent status, or Cardiogenic shock
  • LVEF <40%
  • History of actively malignant disease
  • Patient needing concomitant valvular surgery or other cardiac structural reconstructive surgery
  • As is standard of care, those vessels that are extremely tortuous, very small caliber and/or heavily calcified would not have such wires passed down them. Furthermore, those vessels that are 80-90+% stenosed, with <TIMI 3 flow, which we would not normally pass a diagnostic physiology pressure wire, would not be studied with ComboXT wire.

Sites / Locations

  • East Carolina Heart Institute at Vidant Medical Center

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patients referred for CABG

Arm Description

Patients who after undergoing standard of care diagnostic coronary angiography will be referred for CABG ComboMap XT Guidewire 'SPY' NIRF During CABG

Outcomes

Primary Outcome Measures

Correlation Analysis
Correlation between anatomy, functional anatomy, FFR, SPY® RMP change, and the presence or absence of imaged competitive flow

Secondary Outcome Measures

Full Information

First Posted
May 12, 2014
Last Updated
August 23, 2019
Sponsor
East Carolina University
Collaborators
Volcano Corporation, Imperial College London
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1. Study Identification

Unique Protocol Identification Number
NCT02138305
Brief Title
Correlation Study of Imaging Data Acquired During CABG With Data Acquired in the Cath Lab
Acronym
PERSEUS
Official Title
Collaborative Pilot Study to Determine the Correlation Between Intra-Operative Observations Using SPY® Near Infra-Red Imaging and Cardiac Catheterization Laboratory Physiological Assessment of Lesion Severity (PERSEUS Pilot Study)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
December 2014 (undefined)
Primary Completion Date
March 30, 2018 (Actual)
Study Completion Date
March 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
East Carolina University
Collaborators
Volcano Corporation, Imperial College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Visual assessment of a coronary artery narrowing (called stenosis) seen on angiography is conventionally used to infer how likely the stenosis will limit blood flow (called ischemia) under conditions of increased demand (e.g exercise). This is based on animal work and data from humans with simple single vessel disease with no co-existing conditions. These data have been extrapolated to more complex patients/ complex disease but clearly over-simplifies the situation in the majority of patients cardiologists treat. Pivotal work by DeBruyne, Pils and colleagues in the 90's convincingly showed that pressure derived measurements, called FFR, from the coronary artery during a cardiac catheterization, more accurately identify stenoses that would cause ischemia compared to visual assessment alone. A strategy of FFR guided coronary stenting with drug eluting stents significantly improved outcomes and reduced costs compared to visual assessment alone (FAME trial). Deferring treatment based on FFR has been shown to be safe (DEFER Trial). FFR has excellent sensitivity and specificity. A FFR of <=0.80 was used as this identified ischemia causing lesions 90% of the time. Therefore, the concept of FFR guided percutaneous revascularisation and treatment deferral has a robust evidence base to support it. Coronary bypass grafting (CABG) is traditionally based solely on a visual assessment of angiography images. SPY® Infrared Fluorescence Angiography (NIRF, FDA approved 2005) is used by some cardiac surgeons to assess the patency of bypass grafts in real-time in the operating room, as a surrogate for immediate traditional coronary angiography. Dr. Ferguson observed that regional myocardial perfusion (RMP) image data was also captured in these video sequences. Study Hypotheses: In patients who are likely CABG candidates, target vessel epicardial coronary arteries (TVECAs) with FFR > 0.80 will not demonstrate an increase in RMP despite an anatomically patent bypass conduit during SPY® imaging. In TVECAs with an increase in RMP during SPY® imaging, cardiac catheter laboratory measures of coronary physiology from that TVECA, namely one or a combination of FFR, CFR, HSR and HMR, will correlate with the SPY® data on myocardial perfusion, and suggest a potential mechanism for this physiologic response to TVECA grafting.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Fractional Flow Reserve (FFR), Instantaneous Wave Free Ratio (iFR), Coronary Flow Reserve (CFR), Hyperemic Stenosis Resistance Index (HSR), Hyperemic microvascular resistance (HMR), Wave intensity analysis (WIA), Myocardial Perfusion, SPY NIRF Regional Myocardial Perfusion Analysis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Controlled prospective observational study
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients referred for CABG
Arm Type
Other
Arm Description
Patients who after undergoing standard of care diagnostic coronary angiography will be referred for CABG ComboMap XT Guidewire 'SPY' NIRF During CABG
Intervention Type
Device
Intervention Name(s)
ComboMap XT Guidewire
Intervention Description
Intracoronary pressure and flow measurements
Intervention Type
Procedure
Intervention Name(s)
'SPY' NIRF During CABG
Intervention Description
FDA approved use of injection of indocyanine green for the purposes of performing pre and post coronary grafting graft patency and perfusion assessment with the SPY near infra red fluorescence system
Primary Outcome Measure Information:
Title
Correlation Analysis
Description
Correlation between anatomy, functional anatomy, FFR, SPY® RMP change, and the presence or absence of imaged competitive flow
Time Frame
18 months
Other Pre-specified Outcome Measures:
Title
Correlation Analysis
Description
Correlation analysis between anatomy, functional anatomy, FFR, CFR, HMR and SPY® perfusion data for each TVECA and perfusion territory.
Time Frame
18 months
Title
Instantaneous Wave Free Ratio (iFR)
Description
Offline analysis of de-identified encrypted data for each TVECA interrogated with ComboMap XT wire by Dr Justin Davies's research group, Imperial College, London for iFR determination. Correlation analysis between iFR and presence or absence of imaged competitive flow and intra-operative RMP data on SPY® NIRF
Time Frame
18 months
Title
Wave Intensity Analysis (WIA)
Description
Offline wave wave intensity analysis (WIA) of de-identified encrypted data for each TVECA interrogated with ComboMap XT wire by Dr Justin Davies's research group, Imperial College, London. Correlation analysis between WIA data and presence or absence of imaged competitive flow and intra-operative RMP data on SPY® NIRF
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18<80 Patients with stable angina or NSTEMI with total CK rise of <1000 U/litre who after planned coronary angiography are going to be referred for CABG and have at least one vessel with a visual 40-80% stenosis that is interrogated with intracoronary physiology Exclusion Criteria: Emergent status, or Cardiogenic shock LVEF <40% History of actively malignant disease Patient needing concomitant valvular surgery or other cardiac structural reconstructive surgery As is standard of care, those vessels that are extremely tortuous, very small caliber and/or heavily calcified would not have such wires passed down them. Furthermore, those vessels that are 80-90+% stenosed, with <TIMI 3 flow, which we would not normally pass a diagnostic physiology pressure wire, would not be studied with ComboXT wire.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashesh N Buch, MBChB, MD
Organizational Affiliation
East Carolina University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
T. Bruce Ferguson, MD
Organizational Affiliation
East Carolina University
Official's Role
Principal Investigator
Facility Information:
Facility Name
East Carolina Heart Institute at Vidant Medical Center
City
Greenville
State/Province
North Carolina
ZIP/Postal Code
27834
Country
United States

12. IPD Sharing Statement

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Correlation Study of Imaging Data Acquired During CABG With Data Acquired in the Cath Lab

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