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The Use Of FFR Guided PCI Versus Complete Revascularization and Treatment Of Infarct Related Artery Only In Patients With STEMI (FAIO)

U

University of Limerick

Status and phase

Unknown
Phase 3

Conditions

FFR Guided PCI
Multivessel Coronary Artery Disease
STEMI

Treatments

Procedure: Angio guided PCI
Procedure: FFR guided PCI

Study type

Interventional

Funder types

Other

Identifiers

NCT02637440
FA 2015

Details and patient eligibility

About

In patients with ST elevation myocardial infarction (STEMI) the treatment goal is revascularization of the occluded artery with the use of primary percutaneous coronary intervention (PCI). There is a large subset of patients with STEMI who also have significant disease in arteries other than the site of occlusion, and away from the culprit artery. It is estimated that up to 50% have disease of more than 50% in the non-culprit arteries.

The evidence on how to treat those patients with multi vessel disease is conflicting. Earlier large-scale studies and registries have suggested early and complete revascularization is of no benefit or even harmful. More recent studies have showed the opposite of that. The CVLPRIT study showed that early complete revascularization or preventive PCI reduced primary endpoint of a composite of all cause mortality, myocardial infarction and need for repeat revascularization. The benefit was mainly due to reduced repeat revascularization in the more intensive intervention group. The PRAMI study showed very similar results as well.

The use of Fractional flow Reserve (FFR) in deciding complete revascularization has also showed conflicting results so far. A previous trial showed that FFR guided intervention post STEMI increased MACE. This was conflicted with more recent study, which showed FFR guided complete revascularization improved outcome when compared with more conservative treatment of ischaemia driven intervention.

In this study, the investigators are going to assess the issue of staged revascularization guided by FFR or by angiogram, compared to the standard treatment of ischaemia driven revascularization

Full description

To compare the clinical outcomes measured by composite of mortality, myocardial infarction and repeat revascularization by using FFR guided and angiographically guided revascularization to the standard strategy of ischaemia driven revascularization.

Participants will be allocated to three arms, first conservative group of ischaemia guided PCI, second FFR guided PCI and third angiogram guided PCI where patients where patients with more than 50% lesion will undergo revascularization.

Enrollment

560 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with STEMI and multi-vessel disease on initial angiogram.
  2. Above 18 years of age
  3. Able to give consent

Exclusion criteria

  1. Patients with indication for CABG
  2. Left main stem lesion of >50%
  3. Cardiogenic shock
  4. Intractable angina during hospital admission
  5. Patients with limited life expectancy
  6. Patients with severe chronic kidney disease
  7. Patients with contraindication to dual antiplatelet therapy
  8. Patients with very complex lesions that deemed not favourable for PCI
  9. Pregnancy or childbearing age

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

560 participants in 3 patient groups

Conservative
No Intervention group
Description:
After the index primary PCI. The control group will receive best medical therapy and regular follow up and only PCI for recurrent angina with evidence of inducible ischaemia.
FFR guided
Active Comparator group
Description:
FFR group will undergo FFR at 4 weeks of the index primary PCI as OPD. If FFR is less than 0.8, then PCI will be performed
Treatment:
Procedure: FFR guided PCI
angiogram guided
Active Comparator group
Description:
The group will undergo PCI for all significant lesions more than 50
Treatment:
Procedure: Angio guided PCI

Trial contacts and locations

2

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Central trial contact

Abdullah S Abdullah, MBBS, MRCPI, MSc; Thomas J Kiernan, MD

Data sourced from clinicaltrials.gov

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