Role of FFR in ACS Patients: Pressure ACS Registry

Role of Fractional Flow Reserve Assessment Using Pressure Wire in Patients With Acute Coronary Syndrome Who Treated With Xience Stent; a Multicenter, Prospective, and Observational Registry

Currently, fractional flow reserve (FFR) is regarded as a gold-standard invasive method to define lesion-specific ischemia and FFR-guided PCI has been proven to reduce unnecessary revascularization and to enhance patient's clinical outcomes. Therefore, current guidelines recommend FFR measurement for intermediate coronary stenosis when there is no definite evidence of lesion-specific ischemia. However, previous evidences which well demonstrated the benefit of FFR-guided strategy were mostly generated from patients with stable coronary artery disease.4 FFR may be overestimated and the hemodynamic relevance of a coronary stenosis underestimated in patients with acute coronary syndrome (ACS).Its role in ACS patients still needs to be defined although several studies have recently published addressing the value of FFR-guided PCI in ACS. In fact, recent evidence suggests that culprit lesions of patients presenting with a non-ST-segment elevation myocardial infarction that were deferred based on a "negative" FFR have a relatively high event rate, calling into question the use of FFR in that patient population.

Study Overview

• Status: Active, not recruiting
• Conditions: Acute Coronary Syndrome
• Intervention / Treatment: Device: Fractional Flow Reserve

Detailed Description

STUDY OBJECTIVE

1. To evaluate the impact of FFR on decision for PCI in ACS patients
2. To assess the long term prognosis of deferring PCI based on FFR value in non-culprit lesion; defying the cut-off value of FFR for PCI in the non-culprit lesion of ACS patients
3. To identify the relation between OCT findings and FFR value in culprit and non-culprit lesions of ACS patients
4. To compare the long term prognosis of PCI or deferring PCI based on FFR value in non-culprit lesion of ACS patients
5. To identify OCT findings to predict the lesion progression in deferred lesions.
6. To assess the long term prognosis of post-PCI FFR value in the culprit lesion of NSTE-ACS patients
7. To assess the efficacy of routine use of FFR to guide PCI in ACS patients; angiographically guidance versus FFR guidance

• Study Type: Observational
• Enrollment (Actual): 500

Contacts and Locations

Study Locations

• Korea, Republic of
  • Daejeon, Korea, Republic of
    • Daejeon St.Mary's Hospital
  • Incheon, Korea, Republic of
    • Incheon St.Mary's Hospital
  • Seoul, Korea, Republic of
    • The Catholic University of Korea Seoul St. Mary'S Hospital
  • Gyeonggido
    • Suwon, Gyeonggido, Korea, Republic of
      • St.Vincent's hospital
    • Uijeongbu, Gyeonggido, Korea, Republic of
      • Uijeongbu St.Mary's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: N/A

• Sampling Method: Non-Probability Sample

Study Population

Patients with acute coronary syndrome and intermediate stenosis

Description

Inclusion Criteria:

• Subject age 19-85 years old

  • Diagnosed as ACS (unstable angina/ Non ST elevation myocardial infarction, ST elevation myocardial infarction)

    • At least one stenosis of >50% in a non-culprit vessel ≥ 2.0 mm by visual estimation with TIMI 3 - multivessel disease after PCI for culprit lesion or single vessel disease with ambiguity for PCI ④ FFR within hospitalization for index PCI for ACS

Exclusion Criteria:

• Severe stenosis with TIMI flow ≤ II of the non-IRA artery

  • Cardiogenic shock (Killip class IV) already at presentation or the completion of culprit PCI

    • Intolerance to Aspirin, Clopidogrel, Prasugrel, Ticagrelor, Heparin, Bivaluridin, or Everolimus

      • Known true anaphylaxis to contrast medium (not allergic reaction but anaphylactic shock)

        ⑤ Pregnancy or breast feeding

        ⑥ Non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol noncompliance (per site investigator's medical judgment).

        ⑦ Other primary valvular disease with severe degree: severe mitral regurgitation or mitral stenosis, severe aortic regurgitation or aortic stenosis

        ⑧ Patients with a history of Coronary Artery Bypass Graft(CABG)

        ⑨ Unwillingness or inability to comply with the procedures described in this protocol.

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Rate of Major adverse cardiac events	Rate of the composite of all-cause death, recurrent myocardial infarction	24 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Rate of Major adverse cardiac events at 1 year	Rate of composite of all-cause death, recurrent myocardial infarction	12 months
Rate of Ischemic events	Rate of the composite of all-cause death, recurrent myocardial infarction, and any repeat revascularization	24 months
Rate of Death	Rate of All cause death and cardiac death	24 months
Rate of Repeat revascularization	Rate of Any repeat revascularization	24 months

Collaborators and Investigators

• Sponsor: The Catholic University of Korea
• Investigators: Principal Investigator: Eun Ho Choo, M.D.,PhD, The Catholic University of Korea

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2020
• Primary Completion (Estimated): December 31, 2025
• Study Completion (Estimated): December 31, 2026

Study Registration Dates

• First Submitted: May 31, 2023
• First Submitted That Met QC Criteria: May 31, 2023
• First Posted (Actual): June 9, 2023

Study Record Updates

• Last Update Posted (Actual): October 2, 2024
• Last Update Submitted That Met QC Criteria: October 1, 2024
• Last Verified: October 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Myocardial Ischemia; Heart Diseases; Cardiovascular Diseases; Vascular Diseases; Disease; Syndrome; Acute Coronary Syndrome
• Other Study ID Numbers: PressureACS

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No