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Resting Full-cycle Flow Ratio (RFR) Versus Angiography to Guide Revascularization Strategy in Patients Undergoing Coronary Artery By-pass Grafting (CABG) (RFR-CABG)

Primary Purpose

Coronary Artery Disease

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
RFR guided CABG
Angio guided CABG
Sponsored by
Diagram B.V.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring RFR guided CABG, angiography guided CABG, Graft dysfunction

Eligibility Criteria

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

Inclusion Criteria:

  • All patients between 18 or older undergoing CABG
  • Patients willing and capable to provide written informed consent

Exclusion Criteria:

  • Previous CABG
  • Concomitant severe valvular disease intervention
  • Remaining (expected) coronary stenosis of > 50% diameter stenosis distally to graft anastomosis
  • Left ventricular ejection fraction <30%
  • Known transmural myocardial infarction
  • Documented microvascular disease
  • RFR/FFR measurement judged impossible
  • Life expectancy <2 years
  • Participation in other investigational clinical trials

Sites / Locations

  • Imelda ziekenhuisRecruiting
  • AZ Sint-Jan Brugge
  • Medical University of SilesiaRecruiting
  • SUSCCHRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

angiography guided CABG

RFR guided CABG

Arm Description

angiography guided CABG

RFR guided CABG

Outcomes

Primary Outcome Measures

Number of participants who deceased, had a Myocardial Infarction (MI), Clinically-Driven Target Vessel Revascularization (CD-TVR), Stroke or Graft Dysfunction at 3 months post CABG

Secondary Outcome Measures

Cut-off value for the RFR that best predicts graft occlusion
Number of participants with graft dysfunction at 3 months post CABG
Major adverse cardiac or cerebrovascular event (MACCE), a composite of Death, MI, CD-TVR and Stroke at 1 year
Major adverse cardiac or cerebrovascular event (MACCE), a composite of Death, MI, CD-TVR and Stroke at 3 years
CD-TVR at 3 months post CABG
CD-TVR at 1 year post CABG
CD-TVR at 3 years post CABG

Full Information

First Posted
May 1, 2020
Last Updated
July 8, 2022
Sponsor
Diagram B.V.
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1. Study Identification

Unique Protocol Identification Number
NCT04375306
Brief Title
Resting Full-cycle Flow Ratio (RFR) Versus Angiography to Guide Revascularization Strategy in Patients Undergoing Coronary Artery By-pass Grafting (CABG)
Acronym
RFR-CABG
Official Title
Resting Full-cycle Flow Ratio (RFR) Versus Angiography to Guide Revascularization Strategy in Patients Undergoing Coronary Artery By-pass Grafting (CABG): RFR-CABG Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 3, 2020 (Actual)
Primary Completion Date
October 31, 2024 (Anticipated)
Study Completion Date
June 30, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Diagram B.V.

4. Oversight

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

5. Study Description

Brief Summary
Different trials have shown that fractional flow reserve (FFR) could successfully guide revascularization in patients undergoing percutaneous coronary intervention (PCI). It is conceivable that a similar revascularization guidance could be useful also for surgical revascularization i.e. coronary by-pass graft (CABG). Experience learns that grafts placed on vessels with hemodynamically non-significant stenosis often occlude due to competitive antegrade flow. Resting full-cycle Flow Ratio (RFR) is a measurement performed to evaluate the hemodynamic severity of coronary stenosis. Differently from FFR which is a measurement performed in maximal hyperemia, the RFR is a measurement that is performed in rest and therefore may predict better than FFR the baseline equilibriums that could lead to graft failure, while it has similar capacity to identify hemodynamically significant stenosis as FFR. It is unknown whether RFR guided CABG revascularization is superior as compared to angiography alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
RFR guided CABG, angiography guided CABG, Graft dysfunction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
International prospective randomized multicenter superiority trial
Masking
ParticipantCare ProviderInvestigator
Masking Description
All patients will undergo RFR and FFR measurement before CABG. RFR and FFR values will be blinded to the patients in both arms. In the control arm (angiography guided CABG) the RFR values will be blinded to the cardiothoracic surgeon.
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
angiography guided CABG
Arm Type
Active Comparator
Arm Description
angiography guided CABG
Arm Title
RFR guided CABG
Arm Type
Experimental
Arm Description
RFR guided CABG
Intervention Type
Procedure
Intervention Name(s)
RFR guided CABG
Intervention Description
All patients will undergo RFR and FFR measurement before CABG. RFR and FFR values will be blinded to the patients. In the experimental arm the decision to revascularize will be based on RFR.
Intervention Type
Procedure
Intervention Name(s)
Angio guided CABG
Intervention Description
All patients will undergo RFR and FFR measurement before CABG. RFR and FFR values will be blinded to the patients. In the control arm the RFR values will be blinded to the cardiothoracic surgeon.
Primary Outcome Measure Information:
Title
Number of participants who deceased, had a Myocardial Infarction (MI), Clinically-Driven Target Vessel Revascularization (CD-TVR), Stroke or Graft Dysfunction at 3 months post CABG
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Cut-off value for the RFR that best predicts graft occlusion
Time Frame
Baseline
Title
Number of participants with graft dysfunction at 3 months post CABG
Time Frame
3 months
Title
Major adverse cardiac or cerebrovascular event (MACCE), a composite of Death, MI, CD-TVR and Stroke at 1 year
Time Frame
1 year
Title
Major adverse cardiac or cerebrovascular event (MACCE), a composite of Death, MI, CD-TVR and Stroke at 3 years
Time Frame
3 years
Title
CD-TVR at 3 months post CABG
Time Frame
1 year
Title
CD-TVR at 1 year post CABG
Time Frame
1 year
Title
CD-TVR at 3 years post CABG
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients between 18 or older undergoing CABG Patients willing and capable to provide written informed consent Exclusion Criteria: Previous CABG Concomitant severe valvular disease intervention Remaining (expected) coronary stenosis of > 50% diameter stenosis distally to graft anastomosis Left ventricular ejection fraction <30% Known transmural myocardial infarction Documented microvascular disease RFR/FFR measurement judged impossible Life expectancy <2 years Participation in other investigational clinical trials
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Prof. E. Kedhi, MD, PhD
Phone
+31 384262999
Email
ekedhi@me.com
First Name & Middle Initial & Last Name or Official Title & Degree
S. Postma, PhD
Phone
+31 384262999
Email
rfrcabg.trial@diagram-zwolle.nl
Facility Information:
Facility Name
Imelda ziekenhuis
City
Bonheiden
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr. Dewilde, MD, PhD
Facility Name
AZ Sint-Jan Brugge
City
Brugge
Country
Belgium
Individual Site Status
Active, not recruiting
Facility Name
Medical University of Silesia
City
Katowice
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pawel Gasior, MD
Facility Name
SUSCCH
City
Banská Bystrica
Country
Slovakia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martin Hudec, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
This has not been decided yet.

Learn more about this trial

Resting Full-cycle Flow Ratio (RFR) Versus Angiography to Guide Revascularization Strategy in Patients Undergoing Coronary Artery By-pass Grafting (CABG)

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